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SCARB1 antibody (AA 104-294)

This Mouse Monoclonal antibody specifically detects SCARB1 in WB and IF. It exhibits reactivity toward Human and has been mentioned in 4+ publications.
Catalog No. ABIN968230

Quick Overview for SCARB1 antibody (AA 104-294) (ABIN968230)

Target

See all SCARB1 Antibodies
SCARB1 (Scavenger Receptor Class B, Member 1 (SCARB1))

Reactivity

  • 50
  • 31
  • 29
  • 2
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 49
  • 9
  • 2
Mouse

Clonality

  • 40
  • 20
Monoclonal

Conjugate

  • 38
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
This SCARB1 antibody is un-conjugated

Application

  • 35
  • 19
  • 16
  • 12
  • 10
  • 10
  • 10
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)

Clone

25-CLA
  • Binding Specificity

    • 7
    • 6
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 104-294

    Characteristics

    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.

    Purification

    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

    Immunogen

    Human CLA-1 aa. 104-294

    Isotype

    IgG1
  • Comment

    Related Products: ABIN968535, ABIN967389

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    250 μg/mL

    Buffer

    Aqueous buffered solution containing BSA, glycerol, and ≤0.09 % 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

    -20 °C

    Storage Comment

    Store undiluted at -20°C.
  • Lasley, Narayan, Uittenbogaard, Smart: "Activated cardiac adenosine A(1) receptors translocate out of caveolae." in: The Journal of biological chemistry, Vol. 275, Issue 6, pp. 4417-21, (2000) (PubMed).

    Kozarsky, Donahee, Rigotti, Iqbal, Edelman, Krieger: "Overexpression of the HDL receptor SR-BI alters plasma HDL and bile cholesterol levels." in: Nature, Vol. 387, Issue 6631, pp. 414-7, (1997) (PubMed).

    Acton, Rigotti, Landschulz, Xu, Hobbs, Krieger: "Identification of scavenger receptor SR-BI as a high density lipoprotein receptor." in: Science (New York, N.Y.), Vol. 271, Issue 5248, pp. 518-20, (1996) (PubMed).

    Calvo, Vega: "Identification, primary structure, and distribution of CLA-1, a novel member of the CD36/LIMPII gene family." in: The Journal of biological chemistry, Vol. 268, Issue 25, pp. 18929-35, (1993) (PubMed).

  • Target

    SCARB1 (Scavenger Receptor Class B, Member 1 (SCARB1))

    Alternative Name

    CLA-1

    Background

    CLA-1 (CD36 and LIMPII Analogous-1) is member of a novel gene family that includes CD36, LIMPII, and SR-BI. CD36 is a cell surface glycoprotein that binds to collagen type I and thrombospondin. LIMPII (lysosomal integral membrane protein II), as its name suggests, is expressed on the membrane of lysosomes. SR-BI (scavenger receptor type B class I) is involved in the selective uptake of cholesterol esters. These proteins include two membrane-anchoring regions, two short cytoplasmic tails, and a large extracellular/luminal domain. CLA-1 mRNA is detected in a wide range of tissues including adrenal glands, liver, and testis. Its expression and similarity with other family members suggest it may play a role in HDL metabolism. However, identification of the CLA-1 receptor on monocytes indicates additional CLA-1 functions in leukocytes.
    Synonyms: CD36 and LIMPII Analogous-1

    Molecular Weight

    80 kDa

    Pathways

    Cellular Response to Molecule of Bacterial Origin, Hepatitis C, Lipid Metabolism, SARS-CoV-2 Protein Interactome
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