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Mouse Monoclonal ALB antibody (STJ98462)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB
Recommended dilution: WB 1:1000-1:2000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
ALB antibody, GIG20 antibody, GIG42 antibody, PRO0903 antibody, PRO1708 antibody, PRO2044 antibody, PRO2619 antibody, PRO2675 antibody, UNQ696/PRO1341 antibody,|ALB antibody|Fas (TNFRSF6) binding factor 1 antibody|Fas binding protein 1 antibody|fas-binding factor 1 antibody|FBF 1 antibody|FBF1 antibody|FLJ00103 antibody|KIAA1863 antibody|Protein albatross antibody|Anti-Human Serum Albumin antibody (ab8940)
SCBT cat No: sc-58688|sc-51515|sc-271604|sc-271605|sc-374670|sc-515019|sc-50535|sc-46289|sc-50536|sc-46290|sc-46291|
ALB Monoclonal Antibody
|Catalogue No.|| |
ALB Monoclonal Antibody detects endogenous levels of ALB protein.
Purified recombinant human ALB protein fragments expressed in Ecoli
|Recommended dilution|| |
ALB Antibody was tube-contained. Purified in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
ALB Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Serum albumin antibody
|Protein names|| |
|Protein function|| |
Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca2+, Na+, K+, fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood. Major zinc transporter in plasma, typically binds about 80% of all plasma zinc.
|Protein tissue specificity|| |
|Involvement in disease|| |
Hyperthyroxinemia, familial dysalbuminemic (FDAH) [MIM:615999]: A disorder characterized by abnormally elevated levels of total serum thyroxine (T4) in euthyroid patients. It is due to abnormal serum albumin that binds T4 with enhanced affinity. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Analbuminemia (ANALBA) [MIM:616000]: A rare autosomal recessive disorder manifested by the presence of a very low amount of circulating serum albumin. Affected individuals manifest mild edema, hypotension, fatigue, and, occasionally, lower body lipodystrophy (mainly in adult females). The most common biochemical finding is hyperlipidemia, with a significant increase in the total and LDL cholesterol concentrations, but normal concentrations of HDL cholesterol and triglycerides. . 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|| |
Kenitra variant is partially O-glycosylated at Thr-620. It has two new disulfide bonds Cys-600 to Cys-602 and Cys-601 to Cys-606. / Glycated in diabetic patients. / Phosphorylated by FAM20C in the extracellular medium. / Acetylated on Lys-223 by acetylsalicylic acid.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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