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APOB antibody

This anti-APOB antibody is a Rabbit Polyclonal antibody detecting APOB in IF. Suitable for Human, Mouse and Rat.
Catalog No. ABIN6567867

Quick Overview for APOB antibody (ABIN6567867)

Target

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

Reactivity

  • 107
  • 27
  • 27
  • 7
  • 3
Human, Mouse, Rat

Host

  • 71
  • 49
  • 14
  • 2
  • 2
Rabbit

Clonality

  • 85
  • 51
Polyclonal

Conjugate

  • 62
  • 23
  • 17
  • 7
  • 6
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This APOB antibody is un-conjugated

Application

  • 79
  • 48
  • 43
  • 32
  • 23
  • 17
  • 10
  • 10
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human APOB (NP_000375.2).

    Isotype

    IgG
  • Application Notes

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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.

    Molecular Weight

    Observed_MW: 110kDa

    Calculated_MW: 515kDa

    Gene ID

    338

    UniProt

    P04114

    Pathways

    Lipid Metabolism
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