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Human Serum Albumin mouse mAb

Product code: YP-Ab-02959
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Product introduction

Reactive species
Human
Applications
WB;ELISA;sELISA
Antibody type
Monoclonal antibodies
Gene Name
alb
Protein name
Dalton(DA)
67kD
Immunogen
Purified Human serum albumin.
Specificity
This antibody detects endogenous levels of Serum Albumin and does not cross-react with related proteins.
Constitute
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Source
Monoclonal, Mouse
Dilution rate
wb 1:1000
Purification process
The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
Concentration
mg/ml
Stockpile
-20°C/1 year
Other name
ALB;ALBU_HUMAN;Albumin (32 AA);Albumin (AA 34);Albumin;Analbuminemia;Bisalbuminemia;Cell growth inhibiting protein 42;DKFZp779N1935;Dysalbuminemic hyperthyroxinemia;Growth inhibiting protein 20;HSA;Hyperthyroxinemia dysalbuminemic;PRO0883;PRO0903;PRO1341; PRO2044;PRO2619;Serum albumin.
Background
This gene encodes the most abundant protein in human blood. This protein functions in the regulation of blood plasma colloid osmotic pressure and acts as a carrier protein for a wide range of endogenous molecules including hormones, fatty acids, and metabolites, as well as exogenous drugs. Additionally, this protein exhibits an esterase-like activity with broad substrate specificity. The encoded preproprotein is proteolytically processed to generate the mature protein. A peptide derived from this protein, EPI-X4, is an endogenous inhibitor of the CXCR4 chemokine receptor. [provided by RefSeq, Jul 2016],
Function
caution:A peptide arising from positions 166 to 174 was originally (PubMed:3087352 and PubMed:2437111) termed neurotensin-related peptide (NRP) or kinetensin and was thought to regulates fat digestion, lipid absorption, and blood flow.,disease:A variant structure of albumin could lead to increased binding of zinc resulting in an asymptomatic augmentation of zinc concentration in the blood [MIM:194470].,disease:Defects in ALB are a cause of familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:103600]. FDH is a form of euthyroid hyperthyroxinemia that is due to increased affinity of ALB for T(4). It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population.,function:Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca(2+), Na(+), K(+), fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the collo

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