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APOA1 antibody (N-Term)

This anti-APOA1 antibody is a Chicken Polyclonal antibody detecting APOA1 in WB, IF and EIA. Suitable for Human, Mouse and Rat.
Catalog No. ABIN499311

Quick Overview for APOA1 antibody (N-Term) (ABIN499311)

Target

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

Reactivity

  • 122
  • 38
  • 23
  • 12
  • 12
  • 12
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 99
  • 61
  • 19
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  • 3
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Chicken

Clonality

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Polyclonal

Conjugate

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  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This APOA1 antibody is un-conjugated

Application

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  • 20
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  • 8
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Enzyme Immunoassay (EIA)
  • Binding Specificity

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    N-Term

    Specificity

    This antibody reacts to ApoA1.

    Purification

    Affinity chromatography purified via peptide column

    Immunogen

    ApoA1 antibody was raised against a 17 amino acid peptide from near the amino terminus of human ApoA1.

    Isotype

    IgG
  • Application Notes

    ELISA. Western Blot: ApoA1 antibody can be used for detection of ApoA1 at 1 - 2 μg/mL. Immunofluorescence.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Buffer

    PBS containing 0.02 % sodium azide.

    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

    Storage Comment

    Store the antibody undiluted at 2-8 °C.
  • Target

    APOA1 (Apolipoprotein A-I (APOA1))

    Alternative Name

    Apolipoprotein A I (APO AI)

    Background

    Apolipoprotein A1 (ApoA1) is the major protein component of high density lipoprotein (HDL) in plasma. ApoA1 is synthesized in the liver and small intestine and promotes cholesterol efflux from tissues to the liver for excretion. It is a cofactor for lecithin cholesterolacyltransferase (LCAT), the enzyme responsible for the formation of most plasma cholesteryl esters. Defects in ApoA1 are associated with HDL deficiency, Tangier disease, and systemic non-neuropathic amyloidosis.Synonyms: APOA1, Apo-AI, ApoA-I, ApoAI

    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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