Albumin (PT0561R) PT® Rabbit mAb

    • Catalog No.:YM8377
    • Applications:WB;IHC;IF;IP;ELISA
    • Reactivity:Human; Mouse; Rat;
      • Target:
      • Albumin
      • Fields:
      • >>Thyroid hormone synthesis
      • Gene Name:
      • ALB
      • Protein Name:
      • Serum albumin
      • Human Gene Id:
      • 213
      • Human Swiss Prot No:
      • P02768
      • Mouse Swiss Prot No:
      • P07724
      • Specificity:
      • endogenous
      • Formulation:
      • PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
      • Source:
      • Monoclonal, rabbit, IgG, Kappa
      • Dilution:
      • IHC 1:500-1:2000;WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
      • Purification:
      • Protein A
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • ALB;GIG20;GIG42;Serum albumin
      • Molecular Weight(Da):
      • 69kD
      • Observed Band(KD):
      • 69kD
      • 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
      • Subcellular Location:
      • Secreted
      • Expression:
      • Plasma.
      • Products Images
      • Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-Albumin (PT0561R) antibody. The HRP-conjugated Goat anti-Rabbit IgG(H + L) antibody was used to detect the antibody. Lane 1: huh-7 Lane 2: HepG2 Lane 3: HEK293 Lane 4: Mouse liver Lane 5: Rat liver Predicted band size: 69kDa Observed band size: 69kDa
      • Human hepatocellular carcinoma was stained with anti-Albumin (PT0561R) rabbit antibody
      • Human kidney was stained with anti-Albumin (PT0561R) rabbit antibody
      • Rat kidney was stained with anti-Albumin (PT0561R) rabbit antibody