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APOA1 antibody

The Mouse Monoclonal anti-APOA1 antibody has been validated for EIA and ELISA (Capture). It is suitable to detect APOA1 in samples from Human.
Catalog No. ABIN112523

Quick Overview for APOA1 antibody (ABIN112523)

Target

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

Reactivity

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Human

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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This APOA1 antibody is un-conjugated

Application

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Enzyme Immunoassay (EIA), ELISA (Capture)

Clone

G2
  • Specificity

    Reacts with both free Apolipoprotein A1 and HDL bearing Apo-A1. Does not cross-react with ApoE, ApoB or Albumin.Aff. Const.:Kd = 3nM (for Human Apolipoprotein A1)

    Purification

    Affinity Chromatography on Protein A

    Immunogen

    Native Human Apolipoprotein A1 from Human plasma.

    Isotype

    IgG1
  • Application Notes

    ELISA (1/2.500 - 1/10.000). This antibody is suitable for coating microtitre plates in asandwich ELISA using catalogue number ABIN114061 for detection. Western Blot (1/250 - 1/1000). Immunohistochemistry on frozen sections (1/20 - 1/80).
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Reconstitution

    Restore with 1.0 mL distilled water. Care should be taken during reconstitution as the protein may appear as a film at the bottom of the vial. We recommend that the vial is gently mixed after reconstitution.

    Buffer

    0.01 M Sodium Phosphate, 0.01 M Sodium Borate, 0.11 M Sodium Chloride with 1 % Mannitol and 1 % Dextran.

    Storage

    4 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C. DO NOT FREEZE! This product is photosensitve and should protected from light.
  • Target

    APOA1 (Apolipoprotein A-I (APOA1))

    Alternative Name

    Apolipoprotein A I (APO AI)

    Background

    Apolipoprotein A I promotes cholesterol efflux from tissues to the liver for excretion. Apolipoprotein A I is the major protein component of high density lipoprotein (HDL) in the plasma. Synthesized in the liver and small intestine, it consists of two identical chains of 77 amino acids, an 18 amino acid signal peptide is removed co-translationally and a 6 amino acid propeptide is cleaved post-translationally. Apolipoprotein A I is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. Defects in the Apolipoprotein A I gene are associated with HDL deficiency and Tangier disease. The therapeutic potential of apoA-I has been recently assessed in patients with acute coronary syndromes, using a recombinant form of a naturally occurring variant of apoA-I. The availability of recombinant normal apoA-I should facilitate further investigation into the potential usefulness of apoA-I in preventing atherosclerotic vascular diseases.Synonyms: APOA1, Apo-AI, ApoA-I, ApoAI

    Gene ID

    335

    NCBI Accession

    NP_000030

    UniProt

    P02647

    Pathways

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