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APOB antibody

This Mouse Monoclonal antibody specifically detects APOB in WB, IHC, ELISA and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN865414
$422.30
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 12 to 14 Business Days

Quick Overview for APOB antibody (ABIN865414)

Target

See all APOB Antibodies
APOB (Apolipoprotein B (APOB))

Reactivity

  • 116
  • 27
  • 26
  • 6
  • 2
Human

Host

  • 80
  • 47
  • 14
  • 2
  • 2
Mouse

Clonality

  • 84
  • 60
Monoclonal

Conjugate

  • 62
  • 24
  • 15
  • 7
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This APOB antibody is un-conjugated

Application

  • 86
  • 46
  • 42
  • 31
  • 30
  • 19
  • 17
  • 9
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)

Clone

6G6
  • Purification

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human ApoB expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    WB: 1/500 - 1/2000, IHC: 1/200 - 1/1000, FC: 1/200 - 1/400 ELISA: Propose dilution 1/10000.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    100g/100l

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C
  • Target

    APOB (Apolipoprotein B (APOB))

    Alternative Name

    ApoB

    Background

    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. Synonyms: FLDB, LDLCQ4

    Molecular Weight

    516kDa

    Gene ID

    338

    Pathways

    Lipid Metabolism
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