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Prosaposin antibody (AA 325-524)

PSAP Reactivity: Human WB, ELISA, IHC, FACS, IF/ICC Host: Mouse Monoclonal unconjugated
Catalog No. ABIN1845961
  • Target See all Prosaposin (PSAP) Antibodies
    Prosaposin (PSAP)
    Binding Specificity
    • 15
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 325-524
    Reactivity
    • 37
    • 22
    • 22
    Human
    Host
    • 40
    • 12
    Mouse
    Clonality
    • 42
    • 10
    Monoclonal
    Conjugate
    • 25
    • 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
    • 39
    • 20
    • 14
    • 14
    • 13
    • 11
    • 5
    • 5
    • 5
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (fixed cells) (IF/ICC)
    Purification
    Purified antibody
    Immunogen
    Purified recombinant fragment of human PSAP (AA: 325-524) expressed in E. Coli.
    Isotype
    IgG1
    Top Product
    Discover our top product PSAP Primary Antibody
  • 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 (PSAP Products)
    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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