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APOB antibody

This Rabbit Polyclonal antibody specifically detects APOB in IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7008155

Quick Overview for APOB antibody (ABIN7008155)

Target

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

Reactivity

  • 127
  • 34
  • 33
  • 10
  • 3
Human, Mouse, Rat

Host

  • 90
  • 68
  • 14
  • 2
  • 2
Rabbit

Clonality

  • 97
  • 77
Polyclonal

Conjugate

  • 92
  • 27
  • 21
  • 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

  • 113
  • 81
  • 64
  • 45
  • 44
  • 18
  • 17
  • 13
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    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.

    Gene ID

    338

    UniProt

    P04114

    Pathways

    Lipid Metabolism
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