Aflatoxin M1 is a chemical compound of the aflatoxin class, a group of mycotoxins produced by three species of Aspergillus – Aspergillus flavus, Aspergillus parasiticus, and the rare Aspergillus nomius – which contaminate plant and plant products.
Aspergillus flavus produces only B-type aflatoxins. Aflatoxin M1 is the hydroxylated metabolite of aflatoxin B1 and can be found in milk or milk products obtained from livestock that have ingested contaminated feed. The detection of mycotoxin residues such as Aflatoxin M1 in raw milk is of great concern for the dairy industry because of the potential interfering and adverse effects of mycotoxin residues frequently found in raw milk.
Intended Use
Aflatoxin M1 Quantitative Rapid Test Kit is a lateral flow assay that determines the presence of Aflatoxin M1 residues in raw milk. This test is designed for on-site rapid detection in various enterprises, testing institutions and supervision departments.
96T/Kit
Analyte:Mycotoxin
Samples:Raw milk
Aflatoxin M1 is a chemical compound of the aflatoxin class, a group of mycotoxins produced by three species of Aspergillus – Aspergillus flavus, Aspergillus parasiticus, and the rare Aspergillus nomius – which contaminate plant and plant products.
Aspergillus flavus produces only B-type aflatoxins. Aflatoxin M1 is the hydroxylated metabolite of aflatoxin B1 and can be found in milk or milk products obtained from livestock that have ingested contaminated feed. The detection of mycotoxin residues such as Aflatoxin M1 in raw milk is of great concern for the dairy industry because of the potential interfering and adverse effects of mycotoxin residues frequently found in raw milk.
Intended Use
Aflatoxin M1 Qualitative Rapid Test Kit is a lateral flow assay that determines the presence of Aflatoxin M1 residues in raw milk. This test is designed for on-site rapid detection in various enterprises, testing institutions and supervision departments.
96T/Kit
Analyte:Mycotoxin
Samples:Raw milk
Zeranol, also known as α-zearalanol or simply zearalanol, is a synthetic nonsteroidal estrogen and is used mainly as an anabolic agent in veterinary medicine, and is approved for use as a growth promoter in livestock.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the zeranol in the sample is extracted, filtered, and diluted, and then passed slowly through the zeranol immunoaffinity column. The target substances bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Zeranol is eluted with methanol and then injected into an analytical instrument for detection.
3mL, 25T/50T
Analyte:Mycotoxin
Samples:Dairy product
Aflatoxin M1/M2 is a chemical compound of the aflatoxin class, a group of mycotoxins produced by three species of Aspergillus – Aspergillus flavus, Aspergillus parasiticus, and the rare Aspergillus nomius – which contaminate plant and plant products.
Aspergillus flavus produces only B-type aflatoxins. Aflatoxin M1/M2 is the hydroxylated metabolite of aflatoxin B1/B2 and can be found in milk or milk products obtained from livestock that have ingested contaminated feed. The detection of mycotoxin residues such as Aflatoxin M1/M2 in raw milk is of great concern for the dairy industry because of the potential interfering and adverse effects of mycotoxin residues frequently found in raw milk.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the aflatoxin in the sample is extracted, filtered, and diluted, and then passed slowly through the aflatoxin immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Aflatoxin is eluted with methanol and then injected into an analytical instrument for detection.
3mL, 25T/50T
Analyte:Mycotoxin
Samples:Dairy product
Citrinin is a toxic secondary metabolite produced by a fungus (Monascus monascus). Its main target organ is the kidney, also known as nephrotoxin. At the same time, citrinin is teratogenic. It mainly pollutes red yeast rice products, corn, rice, cheese, etc., which are harmful to human and animal health.
Principle:
The basis of the measurement is the antigen-antibody reaction. Antibodies are connected to the column and the citrinin in the sample is extracted, filtered, and diluted, and then passed slowly through the citrinin immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Citrinin is eluted with methanol, and then injected into the analytical instrument for detection.
3mL, 25T/50T
Analyte:Mycotoxin
Samples:Dairy product
Citrinin is a toxic secondary metabolite produced by a fungus (Monascus monascus). Its main target organ is the kidney, also known as nephrotoxin. At the same time, citrinin is teratogenic. It mainly pollutes red yeast rice products, corn, rice, cheese, etc., which are harmful to human and animal health.
Principle:
The basis of the measurement is the antigen-antibody reaction. Antibodies are connected to the column and the citrinin in the sample is extracted, filtered, and diluted, and then passed slowly through the citrinin immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Citrinin is eluted with methanol, and then injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Grains, red koji products
T-2 toxin (T-2) is a mycotoxin produced by a variety of Fusaria. It mainly pollutes food crops such as wheat, barley, and corn, and their products, and is relatively harmful to human health and cattle industry. HT-2 toxin is the main metabolite of T-2 toxin.
These two toxins are strong inhibitors of protein synthesis in the body and mainly affect the functions of blood, liver, kidney, pancreatic muscle and lymphocytes. The general clinical symptoms after poisoning are anorexia, vomiting, diarrhea, growth arrest, as well as reproduction and neurological dysfunction, etc.
Principle:
The basis of the measurement is the antigen-antibody reaction. Antibodies are connected to the column and after the sample has been pre-treated, it is passed slowly through the immunoaffinity column.
The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. T-2/HT-2 toxins are then eluted with 2% acetic acid-methanol, and then injected into the analytical instrument or derivatized and injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Cereals, feed, vegetable oil
T-2 toxin (T-2) is a mycotoxin produced by a variety of Fusaria. It mainly pollutes food crops such as wheat, barley, and corn, and their products, and is relatively harmful to human health and cattle industry.
Principle:
The basis of the measurement is the antigen-antibody reaction. Antibodies are connected to the column and after the sample has been pre-treated, it is passed slowly through the immunoaffinity column.
The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. T-2/HT-2 toxins are then eluted with 2% acetic acid-methanol, and then injected into the analytical instrument or derivatized and injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Cereals, feed, vegetable oil
Fumonisin is a metabolite produced by Fusarium. It has acute and chronic toxicities, and is species-specific and organ-specific.
Studies have found that high concentrations of fumonisin can cause acute species-specific toxicity symptoms in many domestic and laboratory animals, such as Equine Leukomalacia Syndrome,porcine pulmonary edema, and liver and kidney diseases in sheep. The toxin has also been found to be related to esophageal and liver cancer in humans.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the fumonisin column and the toxins in the sample are extracted, filtered, and passed slowly through the immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Fumonisin then elute with the eluent, and then injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Cereal, peanut, feed, alcohol, condiment, herbs, etc.
Ochratoxin A (OTA) is a toxic metabolite produced by some species of Aspergillus and Penicillium; it is a mycotoxin with high kidney and liver toxicities, and has teratogenic, mutagenic and carcinogenic effects.
Principle:
The basis of the measurement is the antigen-antibody reaction. Antibodies are connected to the Ochratoxin A column and the toxins in the sample are extracted, filtered, and passed slowly through the immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Ochratoxin A is eluted with methanol, and then injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Cereal, peanut, feed, alcohol, condiment, herbs, etc.
DON belongs to the single-endomycin family of molds and is produced by certain Fusarium fungi. 3-ADON and 15-ADON are derivatives of DON.
These toxins are mostly distributed in grain seeds such as wheat, barley, and corn. Due to their high cytotoxicities and immunosuppressive properties, they pose a health threat to humans and animals
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the toxins in the sample are extracted, filtered, and passed slowly through the immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. The toxin is then eluted, blown dry with nitrogen, redissolved and then injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Grains, feed
Deoxynivalenol, also known as vomitoxin, are monoposporin family of fungi, produced by some fusarium fungi.
Vomitoxin are found mainly in wheat, barley, corn and other grains with the level of mg/kg, due to their high cytotoxicity and immunosuppression traits, they hold the threats to humans and animals’ health.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the sample is extracted, filtered, and diluted, and then passed slowly through the deoxynivalenol immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Deoxynivalenol is eluted with methanol, and then dried with nitrogen and injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Grains, feed, alcohol, etc.
Zearalenone (ZEN), also known as F-2 toxin, is mainly produced by Fusarium strains. Its components are 2,4-dihydroxybenzoic acid lactones produced by Fusarium graminearum and Fusarium culmorum.
ZEN mainly pollutes crops such as corn, wheat, and grains. It has a strong estrogenic effect and can cause hyperestrogen, as well as severe reproductive tract symptoms and infertility, and is also immunotoxic and genotoxic.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the toxins in the sample are extracted, filtered, and passed slowly through the zearalenone immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Zearalenone is eluted with methanol, and then injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Grains, feed
Aflatoxins are toxic metabolites of a class of fungi (such as Aspergillus flavus and Aspergillus parasiticus). They are highly carcinogenic and are found mainly in grains, peanuts, nuts, cottonseeds, animal feed, vegetable oils, as well as animal tissues and blood.
Among them, Aflatoxin B1 (AFT B1) ranks first in terms of toxicity, carcinogenicity and frequency of contamination.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the aflatoxin in the sample is extracted, filtered, and diluted, and then passed slowly through the aflatoxin immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Aflatoxin is eluted with methanol, and then injected into the analyticalinstrument for detection.
Analyte:Mycotoxin
Samples:Food, oil, nut, feed, herbs, tea, dairy product, etc.
Aflatoxins are toxic metabolites of a class of fungi (such as Aspergillus flavus and Aspergillus parasiticus). They are highly carcinogenic and are found mainly in grains, peanuts, nuts, cottonseeds, animal feed, vegetable oils, as well as animal tissues and blood.
Among them, Aflatoxin B1 (AFT B1) ranks first in terms of toxicity, carcinogenicity and frequency of contamination. Aflatoxin M1 is a hydroxylated metabolite of Aflatoxin B1 and a strong carcinogen. Cow milk and its products are prone to Aflatoxin M1 contamination.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the aflatoxin in the sample is extracted, filtered, and diluted, and then passed slowly through the aflatoxin immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Aflatoxin is eluted with methanol, and then injected into the analytical instrument for detection.
Analyte:Mycotoxin
Samples:Food, oil, nut, feed, herbs, tea, dairy product, etc.
Aflatoxins are toxic metabolites of a class of fungi (such as Aspergillus flavus and Aspergillus parasiticus). They are highly carcinogenic and are found mainly in grains, peanuts, nuts, cottonseeds, animal feed, vegetable oils, as well as animal tissues and blood.
Among them, Aflatoxin B1 (AFT B1) ranks first in terms of toxicity, carcinogenicity and frequency of contamination.
Principle:
The basis of the measurement is the antigen-antibody reaction.
Antibodies are connected to the column and the aflatoxin in the sample is extracted, filtered, and diluted, and then passed slowly through the aflatoxin immunoaffinity column. The toxins bind to the antibodies in the column and the immunoaffinity column is then washed to remove other unrelated substances that have not been bound. Aflatoxin is then eluted with methanol and injected into an analytical instrument for detection.
Analyte:Mycotoxin
Samples:Food,oil, nut, feed, herbs, tea, etc.
Zearalenone (ZEN) is a potent fungal toxin that affects crops grown or stored in cool and moist conditions. Zearalenone is known to cause estrogenic effects such as precocious development in swine.
The toxin is formed by the Fusarium species and mainly affects corn, wheat, sorghum, barley and rye. Such Fusarium species are known to co-produce other toxins such as deoxynivalenol.
Intended Use
The Zearalenone ELISA Kit is a competitive ELISA for the qualitative or quantitative analysis of Zearalenone in feed and feed material.
Analyte:Mycotoxin
Samples:liquid milk, milk powder, fermented milk,cheese, milk beverage
Deoxynivalenol is known as vomitoxin or DON. It is a potent fungal toxin to affect crops grown in cool and moist conditions. Fusarium graminearum is the principal DON-producing fungus in grains but Fusarium culmorum is often involved as well especially in certain geographical areas of the world.
Deoxynivalenol is a known immunosuppressant and may cause kidney problems. Consuming DON-contaminated grain can cause vomiting in humans and animals.
Intended Use
The Deoxynivalenol ELISA Kit is a competitive ELISA for the qualitative or quantitative analysis of Deoxynivalenol in rice flour, wheat, barley, corn, flour, oats etc.
Analyte:Mycotoxin
Samples:liquid milk, milk powder, fermented milk,cheese, milk beverage
Ochratoxin A (OTA) is a toxic metabolite produced by Aspergillus flavus and Penicillium genera. Ochratoxin A has a strong liver and kidney toxicity, and has teratogenic, mutagenic and carcinogenic.
OTA is the second important and harmful mycotoxin in the family following with Aflatoxin flavus. As the OTA producing fungi exist widely in nature, especially higher yield in cereals and cereals products, coffee, cocoa contaminated with OTA, it has been potential threat for human health and development of animal husbandry.
Intended Use
The Ochratoxin A ELISA Kit is an indirect competitive ELISA for the quantitative analysis of Ochratoxin A in grain, feed, etc.
Analyte:Mycotoxin
Samples:liquid milk, milk powder, fermented milk, cheese, milk beverage
Fumonisin is one of the mycotoxins produced by F. Moniliforme. And has 28 derivatives. FB is the most universal one of the derivatives, which mainly contaminate corn and their products. FB has a toxin effects to animals because of its powerful toxicity. As study shown that FB can cause the Leukoencephalopathy softening syndrome of horses and Pulmonary edema syndrome of pigs and can also induce human esophageal cancer, liver cancer, gastric cancer and other diseases, so it poses a threat to husbandry and human health.
This kit is toxin detection products from the latest ELISA technology research and development, it has advantages of rapid, simple, accurate and high sensitivity compared with the instrument analysis technology, and its operation time only 15 min and also can minimize the work intensity and operation error.
Intended Use
FB ELISA Kit is an indirect competitive ELISA kit for the quantitative analysis of fumonisins in feed, corn and corn by- products.
Analyte:Mycotoxin
Samples:Corn, wheat, compound feed, cattle fine feed, corn by-product
Fumonisin is one of the mycotoxins produced by F. Moniliforme. And has 28 derivatives. FB is the most universal one of the derivatives, which mainly contaminate corn and their products. FB has a toxin effects to animals because of its powerful toxicity.
As study shown that FB can cause the Leukoencephalopathy softening syndrome of horses and Pulmonary edema syndrome of pigs and can also induce human esophageal cancer, liver cancer, gastric cancer and other diseases, so it poses a threat to husbandry and human health.
Intended Use
The kit is a one-step lateral flow immunochromatographic assay that determines a quantitative level for the presence of Fumonisins and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, feed raw material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Ochratoxin A (OTA) is a toxic metabolite produced by Aspergillus flavus and Penicillium genera. Ochratoxin A has a strong liver and kidney toxicity, and has teratogenic, mutagenic, and carcinogenic.
OTA was considered to be the second important and harmful mycotoxin in the family following with Aflatoxin flavus. As the OTA producing fungi exist widely in nature, especially higher yield in cereals and cereals products, coffee, cocoa contaminated with OTA, it has been potential threat for human health and development of animal husbandry.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a quantitative level for the presence of Ochratoxin A and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, feed raw material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Deoxynivalenol is known as vomitoxin or DON. It is a potent fungal toxin to affect crops grown in cool and moist conditions. Fusarium graminearum is the principal DON-producing fungus in grains but Fusarium culmorum is often involved as well especially in certain geographical areas of the world. Deoxynivalenol is a known immunosuppressant and may cause kidney problems. Consuming DON-contaminated grain can cause vomiting in humans and animals.
Deoxynivalenol is formed by the Fusarium species and mainly affects corn, wheat, oats and barley.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a quantitative level for the presence of deoxynivalenol and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, feed raw material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
The mycotoxin zearalenone is formed by fungi of the genus fusarium and mainly affects corn, wheat, sorghum, barley and rye. Zearalenone is a phytohormone which displays, apart from its anabolic properties, mainly estrogenic effects.
Because of its estrogenic properties, zearalenone may induce fertility disorders in animals with clinical signs of hyperestrogenism – an aspect of a disease which although reported mainly in hogs, is described in other species such as cow, horse and sheep.
Intended Use
The kit is a one-step lateral flow immunochromatographic assay that determines a quantitative level for the presence of zearalenone and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, feed raw material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Aflatoxins are toxic and carcinogenic. They are metabolites of the fungi Aspergillus flavus and Aspergillus parasiticus.
There are four principle types of aflatoxin: B1, B2, G1 and G2, which are named for their respective innate fluorescent properties. Aflatoxins can be found mainly in cereals, nuts, cottonseed and human blood.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a quantitative level for the presence of Aflatoxin B1 and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Aflatoxins are toxic and carcinogenic. They are metabolites of the fungi Aspergillus flavus and Aspergillus parasiticus.
There are four principle types of aflatoxin: B1, B2, G1 and G2, which are named for their respective innate fluorescent properties. Aflatoxins can be found mainly in cereals, nuts, cottonseed and human blood.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a quantitative level for the presence of Aflatoxin B1 and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
T2 toxin is a trichothecene mycotoxin initially produced by species of Fusarium. T2 toxin is often found in grains and grain products such as cereals and breads.
T2 toxin may act as an anticoagulant at low doses, decreasing fibrinolytic and coagulant signaling pathways. In vivo, T2 toxin alters permeability of the blood-brain barrier (BBB). In the brain and spleen, T2 toxin induces oxidative stress by decreasing levels of glutathione and increasing levels of ROS and lipid peroxidation; it also decreases expression of tissue inhibitor of metalloproteinase 1 (TIMP-1) and increases expression of matrix metalloproteinase 9 (MMP9), TNF-α, IL-1β, and IL-6. In vitro, T2 toxin alters steroidogenesis by inhibiting production of follicular-stimulating hormone (FSH) and progesterone and inhibiting the stimulatory effects of IFG-1.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a quantitative level for the presence of T-2 Toxin and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
T2 toxin is a trichothecene mycotoxin initially produced by species of Fusarium. T2 toxin is often found in grains and grain products such as cereals and breads.
T2 toxin may act as an anticoagulant at low doses, decreasing fibrinolytic and coagulant signaling pathways. In vivo, T2 toxin alters permeability of the blood-brain barrier (BBB). In the brain and spleen, T2 toxin induces oxidative stress by decreasing levels of glutathione and increasing levels of ROS and lipid peroxidation; it also decreases expression of tissue inhibitor of metalloproteinase 1 (TIMP-1) and increases expression of matrix metalloproteinase 9 (MMP9), TNF-α, IL-1β, and IL-6. In vitro, T2 toxin alters steroidogenesis by inhibiting production of follicular-stimulating hormone (FSH) and progesterone and inhibiting the stimulatory effects of IFG-1.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a quantitative level for the presence of T-2 Toxin and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Fumonisin is one of the mycotoxins produced by F. Moniliforme. And has 28 derivatives. FB is the most universal one of the derivatives, which mainly contaminate corn and their products. FB has a toxin effects to animals because of its powerful toxicity.
As study shown that FB can cause the Leukoencephalopathy softening syndrome of horses and Pulmonary edema syndrome of pigs and can also induce human esophageal cancer, liver cancer, gastric cancer and other diseases, so it poses a threat to husbandry and human health.
Intended Use
The kit is a one-step lateral flow immunochromatographic assay that determines a qualitative level for the presence of Fumonisins and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
The mycotoxin zearalenone is formed by fungi of the genus fusarium and mainly affects corn, wheat, sorghum, barley and rye. Zearalenone is a phytohormone which displays, apart from its anabolic properties, mainly estrogenic effects.
Because of its estrogenic properties, zearalenone may induce fertility disorders in animals with clinical signs of hyperestrogenism – an aspect of a disease which although reported mainly in hogs, is described in other species such as cow, horse and sheep.
Intended Use
The kit is a one-step lateral flow immunochromatographic assay that determines a qualitative level for the presence of zearalenone and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Intended Use
Aflatoxin M1 Rapid Test Kit is a lateral flow assay that determines a qualitative level for the presence of aflatoxin M1 in raw cow’s milk.
This test is designed for rapid field use or daily control in laboratories.
Analyte:Mycotoxin
Samples:Milk
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Deoxynivalenol is known as vomitoxin or DON. It is a potent fungal toxin to affect crops grown in cool and moist conditions.
Fusarium graminearum is the principal DON-producing fungus in grains but Fusarium culmorum is often involved as well especially in certain geographical areas of the world. Deoxynivalenol is a known immunosuppressant and may cause kidney problems. Consuming DON-contaminated grain can cause vomiting in humans and animals. Deoxynivalenol is formed by the Fusarium species and mainly affects corn, wheat, oats and barley.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a qualitative level for the presence of deoxynivalenol and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some of finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Ochratoxin A (OTA) is a toxic metabolite produced by Aspergillus flavus and Penicillium genera. Ochratoxin A has a strong liver and kidney toxicity, and has teratogenic, mutagenic, and carcinogenic.
OTA was considered to be the second important and harmful mycotoxin in the family following with Aflatoxin flavus. As the OTA producing fungi exist widely in nature, especially higher yield in cereals and cereals products, coffee, cocoa contaminated with OTA, it has been potential threat for human health and development of animal husbandry.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a qualitative level for the presence of Ochratoxin A and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some of finished feed products.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Aflatoxins are toxic and carcinogenic. They are metabolites of the fungi Aspergillus flavus and Aspergillus parasiticus.
There are four principle types of aflatoxin: B1, B2, G1 and G2, which are named for their respective innate fluorescent properties. Aflatoxins can be found mainly in cereals, nuts, cottonseed and so on.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a qualitative level for the presence of Aflatoxin B1 and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some finished feed and Vegetable oil
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
T2 toxin is a trichothecene mycotoxin initially produced by species of Fusarium. T2 toxin is often found in grains and grain products such as cereals and breads. T2 toxin may act as an anticoagulant at low doses, decreasing fibrinolytic and coagulant signaling pathways.
In vivo, T2 toxin alters permeability of the blood-brain barrier (BBB). In the brain and spleen, T2 toxin induces oxidative stress by decreasing levels of glutathione and increasing levels of ROS and lipid peroxidation; it also decreases expression of tissue inhibitor of metalloproteinase 1 ( TIMP-1) and increases expression of matrix metalloproteinase 9 (MMP9), TNF-α, IL-1β, and IL-6. In vitro, T2 toxin alters steroidogenesis by inhibiting production of follicular-stimulating hormone (FSH) and progesterone and inhibiting the stimulatory effects of IFG-1.
Intended Use
FB ELISA Kit is an indirect competitive ELISA kit for the quantitative analysis of fumonisins in feed, corn and corn by-products.
Analyte:Mycotoxin
Samples: Corn, wheat, compound feed, cattle fine feed, corn by-product
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Aflatoxins are toxic and carcinogenic. They are metabolites of the fungi Aspergillus flavus and Aspergillus parasiticus.
There are four principle types of aflatoxin: B1, B2, G1 and G2, which are named for their respective innate fluorescent properties. Aflatoxin B1 is the most frequently encountered of the group and the most toxic one. Aflatoxins can be found mainly in milk, cereals, nuts, cottonseed and human blood.
Aflatoxin B1 is a potent human carcinogen and may contribute to human liver cancer.
Intended Use
The Aflatoxin B1 ELISA Test Kit is a competitive ELISA for the qualitative or quantitative analysis of aflatoxin B1 in rice flour, milk etc.
Analyte:Mycotoxin
Samples:Peanut, feed, edible oil, corn and other grains
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.
Aflatoxins are toxic and carcinogenic. They are metabolites of the fungi Aspergillus flavus and Aspergillus parasiticus.
There are four principle types of aflatoxin: B1, B2, G1 and G2, which are named for their respective innate fluorescent properties. Aflatoxins can be found mainly in cereals, nuts, cottonseed and human blood.
Intended Use
For the quantitative analysis of aflatoxin in grain, nuts, cottonseed and feed products.
Analyte:Mycotoxin
Samples:Peanut, feed, edible oil, corn and other grains
1. Reagents should be brought to room temperature, 20–25ºC prior to use. Avoid prolonged (> 24 hours) storage at room temperature.
2. Immediately start the next step of operation after the washing procedure, avoid the microwell be dry affecting the detecting result.
3. Shake the reagent before use.
4. The Stop Solution is 2M sulphuric acid. Avoid contact with skin and mucous membranes. Immediately clean up any spills and wash area with copious amounts of water. If contact should occur, immediately flush with copious amounts of water.
5. Do not use reagents after expiration date. Do not substitute reagents from any other manufacturer into the test kit. Do not combine reagents from other Mycotoxin ELISA Kits with different Lot numbers.
6. The kit should be store at the temperature 2-8℃, do not freeze. Be sure to re-seal unused wells in the zip-lock bag with desiccant stored. Avoid directly exposure the reagents to light.
7. Any color conversion indicates that the reagent is deteriorated, please drop it. If the absorbance of negative control absorbance is less than 0.5, the reagent is probably deteriorated.
8. The incubating time is usually 15-20 minutes after dispensing Substrate A and 50µL Substrate B into the wells. If the color too less, please prolong the incubating time but should not exceed 30 minutes. Conversely, reduce the incubating time.
9. Crystallization of the Concentrated Wash buffer is a normal phenomenon, heat it before using.
10. The optimum reaction temperature is 25℃, too high or two low temperature would arise the change of the absorbance and sensitivity.
Aflatoxins are toxic and carcinogenic. They are metabolites of the fungi Aspergillus flavus and Aspergillus parasiticus.
There are four principle types of aflatoxin: B1, B2, G1 and G2, which are named for their respective innate fluorescent properties. Aflatoxins can be found mainly in cereals, nuts, cottonseed and so on.
Intended Use
The kit is a lateral flow immunochromatographic assay that determines a qualitative level for the presence of Aflatoxin B1 and is intended for use in grains, feed materials and feed products. This method is suitable for the rapid on-site test.
Analyte:Mycotoxin
Samples:Grain, raw feed material, some of finished feed.
1. Adhere to the instructions of test procedures.
2. Store test kits at 4-30˚C when not in use, and do not use the kits beyond the expiration date.
3. Please don’t touch the membrane on the strips.
4. Remove microwell sealer slightly to prevent the powder from being released from the wells.
5. Avoid direct sunlight and direct blows during testing.
6. Do not re-use pipette tips, test strips or microwells.
7. The unsealed microwells should be used within 1 hour.
8. This test method is just used for rapid screening purpose; if positive results are occurred,please verify them by a quantitative method.
9. Methanol/ Ethanol are flammable. Caution must be taken in its use and storage.
10. Please avoid direct sunlight or blowing when testing.
11. Do not take tap-water, distilled water or deionized water as a negative control.
12. Considering that all materials, containers and devices exposed to the sample are contaminated with toxins, please wear protective gloves and safety glasses while using a kit.
13. The components in this test kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers.
14. If the sample extract is too alkaline (pH>9) or acid (pH<5), please adjust the pH value of the sample extract to be 6.0-8.0 by using NaOH or HCl (2.0 mol/L) before dilution.
15. Any problem encountered during usage, please contact with the supplier.