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APOB antibody

This anti-APOB antibody is a Rabbit Polyclonal antibody detecting APOB in IHC and ELISA. Suitable for Human.
Catalog No. ABIN7189848

Quick Overview for APOB antibody (ABIN7189848)

Target

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

Reactivity

  • 127
  • 35
  • 34
  • 10
  • 3
Human

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
  • 80
  • 64
  • 45
  • 43
  • 18
  • 17
  • 14
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of Human APOB

    Isotype

    IgG
  • Application Notes

    ELISA:1:1000-1:5000, IHC:1:15-1:50,

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

    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,-80 °C

    Storage Comment

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    APOB (Apolipoprotein B (APOB))

    Alternative Name

    APOB

    Background

    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.

    Aliases: Apo B 100 antibody, Apo B antibody, Apo B-100 antibody, Apo B-48 antibody, Apo B100 antibody, Apo B48 antibody, ApoB 100 antibody, ApoB 48 antibody, APOB antibody, APOB_HUMAN antibody, Apolipoprotein B (including Ag(x) antigen) antibody, Apolipoprotein B 100 antibody, Apolipoprotein B 48 antibody, Apolipoprotein B antibody, Apolipoprotein B-48 antibody, Apolipoprotein B100 antibody, Apolipoprotein B48 antibody, FLDB antibody, LDLCQ4 antibody

    UniProt

    P04114

    Pathways

    Lipid Metabolism
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