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APOA1 antibody

This Rabbit Polyclonal antibody specifically detects APOA1 in WB, IHC and IF. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7255570

Quick Overview for APOA1 antibody (ABIN7255570)

Target

See all APOA1 Antibodies
APOA1 (Apolipoprotein A-I (APOA1))

Reactivity

  • 134
  • 43
  • 28
  • 22
  • 17
  • 13
  • 6
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Mouse

Host

  • 115
  • 83
  • 19
  • 5
  • 3
  • 3
  • 2
Rabbit

Clonality

  • 139
  • 90
Polyclonal

Conjugate

  • 134
  • 38
  • 17
  • 11
  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This APOA1 antibody is un-conjugated

Application

  • 165
  • 101
  • 82
  • 72
  • 65
  • 20
  • 12
  • 11
  • 9
  • 8
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human APOA1 (NP_000030.1).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IHC 1:50-1:100 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

    APOA1 (Apolipoprotein A-I (APOA1))

    Alternative Name

    APOA1

    Background

    This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The encoded preproprotein is proteolytically processed to generate the mature protein, which promotes cholesterol efflux from tissues to the liver for excretion, and is a cofactor for lecithin cholesterolacyltransferase (LCAT), an enzyme responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein.

    Molecular Weight

    Observed_MW: 31 kDa

    Calculated_MW: 30 kDa

    Gene ID

    335

    UniProt

    P02647

    Pathways

    Regulation of Lipid Metabolism by PPARalpha, Production of Molecular Mediator of Immune Response, Lipid Metabolism
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