Aflatoxin (AFM1+AFB1) Rat Monoclonal Antibody [Clone ID: 1C6]

Specifications

Product Data
Clone Name	1C6
Applications	ELISA
Recommend Dilution	ELISA (Indirect): Reactive to Aflatoxin M1 (AFM1) and Aflatoxin B1 (AFB1).  Fluorimetric Immunoassay: Reactive to Aflatoxin M1 (AFM1) and Aflatoxin M2 (AFM2) (See Reference 1).
Host	Rat
Clonality	Monoclonal
Immunogen	Aflatoxin M1-BSA conjugate
Specificity	The selected monoclonal antibodies are reactive to Aflatoxin M1 (AFM1) and Aflatoxin B1 (AFB1), but not reactive to BSA and other irrelevant antigens by ELISA. Similarly, a competitive binding assay using AFM1 as binding competitor to compete with AFM1-BSA-125I showed that AFM1 can effectively inhibit the binding of this monoclonal to AFM1-BSA-125I and the inhibition degree corresponded to the amounts of AFM1 used.
Formulation	0.01M PBS, pH 7.2 without preservatives State: Purified State: Lyophilized purified Ig fraction
Reconstitution Method	Restore in double distillated water to adjust the final concentration to 1.0 mg/ml
Concentration	1.0 mg/ml (after reconstitution)
Purification	Affinity Chromatography on protein G
Conjugation	Unconjugated
Storage Condition	Prior to reconstitution store at 2-8°C for one month or at -20°C for longer. Following reconstitution store undiluted at 2-8°C for two weeks or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing.
Background	The aflatoxins are a group of closely related mycotoxins that are widely distributed in nature. The most important of the group is aflatoxin B1 (AFB1), which has a range of biological activities, including acute toxicity, teratogenicity, mutagenicity and carcinogenicity. In order for AFB1 to exert its effects, it must be converted to its reactive epoxide by the action of the mixed function mono-oxygenase enzyme systems (cytochrome P450-dependent) in the tissues (in particular, the liver) of the affected animal. This epoxide is highly reactive and can form derivatives with several cellular macromolecules, including DNA, RNA and protein. Cytochrome P450 enzymes may additionally catalyse the hydroxylation (to AFQ1 and AFM1) and demethylation (to AFP1) of the parent AFB1 molecule, resulting in products less toxic than AFB1. Conjugation of AFB1 to glutathione (mediated by glutathione S-transferase) and its subsequent excretion is regarded as an important detoxification pathway in animals.
Reference Data

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