PSAP (Human) Matched Antibody Pair

Catalog # H00005660-AP11

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Size:1 Set
Price: USD $ 607.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human PSAP.

    Reactivity

    Human

    Quality Control Testing

    Standard curve using recombinant protein ( H00005660-P02 ) as an analyte.

    Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-PSAP (100 ug)
    2. Detection antibody: mouse monoclonal anti-PSAP, IgG2a Kappa (20 ug)
    *Reagents are sufficient for at least 1-2 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Recombinant protein)

  • Gene Info — PSAP

    Entrez GeneID

    5660

    Gene Name

    PSAP

    Gene Alias

    FLJ00245, GLBA, MGC110993, SAP1

    Gene Description

    prosaposin

    Omim ID

    176801 249900 610539

    Gene Ontology

    Hyperlink

    Gene Summary

    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. [provided by RefSeq

    Other Designations

    OTTHUMP00000019776|sphingolipid activator protein-1

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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