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Mouse Monoclonal AFP antibody [6E6] (STJ97817)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-1:2000; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for AFP Monoclonal Antibody.
Check alternative names for the antibodyExpand
AFP antibody, HPAFP antibody,|Afp antibody|Alpha fetoglobulin antibody|Alpha fetoprotein antibody|Alpha fetoprotein precursor antibody|Alpha-1-fetoprotein antibody|Alpha-fetoglobulin antibody|Alpha-fetoprotein antibody|alpha-fetoprotein, Hereditary persistence of, included antibody|FETA antibody|FETA_HUMAN antibody|Hereditary persistence of alpha fetoprotein antibody|HPAFP antibody|Anti-alpha 1 Fetoprotein antibody [AFP-01] (ab3980)
SCBT cat No: sc-80464|sc-130302|sc-69857|sc-51506|sc-8108|sc-8399|sc-166450|sc-166325|sc-15375|sc-166335|
AFP Monoclonal Antibody
|Catalogue No.|| |
AFP Monoclonal Antibody detects endogenous levels of AFP protein.
Purified recombinant fragment of human AFP expressed in E Coli
|Recommended dilution|| |
WB 1:500-1:2000; ELISA 1:10000
AFP Antibody was tube-contained. Antibody are purified by protein G affinity chromatography. Liquid in PBS containing 50% glycerol and 0.03% sodium azide.
AFP Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Alpha-fetoprotein antibody, Alpha-1-fetoprotein antibody, Alpha-fetoglobulin antibody
|Protein names|| |
Alpha-fetoprotein , Alpha-1-fetoprotein , Alpha-fetoglobulin
|Protein function|| |
Binds copper, nickel, and fatty acids as well as, and bilirubin less well than, serum albumin. Only a small percentage (less than 2%) of the human AFP shows estrogen-binding properties.
|Protein tissue specificity|| |
Plasma. Synthesized by the fetal liver and yolk sac.
|Involvement in disease|| |
Alpha-fetoprotein deficiency (AFPD) [MIM:615969]: A benign condition characterized by undetectable AFP levels in the amniotic fluid. Affected individuals are asymptomatic and present normal development. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Alpha-fetoprotein, hereditary persistence (HPAFP) [MIM:615970]: A benign autosomal dominant condition characterized by continued expression of alpha-fetoprotein in adult life. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the ALB/AFP/VDB family. / Contains 3 albumin domains.
|Protein post-translational modifications|| |
Independent studies suggest heterogeneity of the N-terminal sequence of the mature protein and of the cleavage site of the signal sequence. / Sulfated.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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