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Prosaposin antibody (AA 325-524)

This Mouse Monoclonal antibody specifically detects Prosaposin in WB, IHC, ELISA, FACS and IF/ICC. It exhibits reactivity toward Human.
Catalog No. ABIN1845961

Quick Overview for Prosaposin antibody (AA 325-524) (ABIN1845961)

Target

See all Prosaposin (PSAP) Antibodies
Prosaposin (PSAP)

Reactivity

  • 51
  • 23
  • 22
Human

Host

  • 46
  • 20
Mouse

Clonality

  • 47
  • 19
Monoclonal

Conjugate

  • 39
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Prosaposin antibody is un-conjugated

Application

  • 53
  • 27
  • 23
  • 14
  • 14
  • 14
  • 12
  • 11
  • 9
  • 6
  • 5
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS), Immunofluorescence (fixed cells) (IF/ICC)
  • Binding Specificity

    • 15
    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 325-524

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human PSAP (AA: 325-524) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.0 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 0.5 % protein stabilizer.

    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

    Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
  • Target

    Prosaposin (PSAP)

    Alternative Name

    PSAP

    Background

    This gene encodes a highly conserved glycoprotein which is a precursor for 4 cleavage products: saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease, Tay-Sachs disease, and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants encoding different isoforms.

    Molecular Weight

    58.1 kDa

    Gene ID

    5660

    UniProt

    P07602

    Pathways

    Positive Regulation of Endopeptidase Activity
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