ALB Monoclonal Antibody

    • Catalog No.：YM1006
    • Applications：WB
    • Reactivity：Human
      • 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
      • Immunogen：
      • Purified recombinant human ALB protein fragments expressed in E.coli.
      • Specificity：
      • ALB Monoclonal Antibody detects endogenous levels of ALB protein.
      • Formulation：
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source：
      • Monoclonal, Mouse
      • Dilution：
      • WB 1:1000 - 1:2000. Not yet tested in other applications.
      • Purification：
      • Affinity purification
      • Concentration：
      • 1 mg/ml
      • 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
      • 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
      • Western Blot analysis using ALB Monoclonal Antibody against human albumin whole cell lysate.

      Attributes

      • Code：
      • YM1006
      • Size
      • 50μL / 100μL / 200μL
      • Price$：
      • 210 / 350 / 600
      • Delivery：
      • 2024-12-31
      Order

      Related Products