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WB analysis of human serum lysates using GTX88654 Apolipoprotein B antibody, Internal. This antibody showed background below 150kDa in serum samples. Dilution : 0.5microg/ml
WB analysis of human serum lysates using GTX88654 Apolipoprotein B antibody, Internal. This antibody showed background below 150kDa in serum samples. Dilution : 0.5microg/ml
WB analysis of human serum lysates using GTX88654 Apolipoprotein B antibody, Internal. This antibody showed background below 150kDa in serum samples. Dilution : 0.5microg/ml

Apolipoprotein B antibody, Internal

GTX88654
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetAPOB
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Overview

  • Supplier
    GeneTex
  • Product Name
    Apolipoprotein B antibody, Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.3-1microg/ml. IHC-P: 2microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID338
  • Target name
    APOB
  • Target description
    apolipoprotein B
  • Target synonyms
    apoB-100; apoB-48; apolipoprotein B (including Ag(x) antigen); apolipoprotein B-100; apolipoprotein B48; FCHL2; FLDB; LDLCQ4
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP04114
  • Protein Name
    Apolipoprotein B-100
  • Scientific Description
    This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203