PSAP polyclonal antibody (A01)

Catalog # H00005660-A01

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Size:50 uL
Price: USD $ 243.00
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  • +1-909-264-1399
    +1-909-992-0619
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QC Test

Western Blot detection against Immunogen (81.88 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a full-length recombinant PSAP.

    Immunogen

    PSAP (AAH01503, 18 a.a. ~ 524 a.a) full-length recombinant protein with GST tag.

    Sequence

    PVLGLKECTRGSAVWCQNVKTASDCGAVKHCLQTVWNKPTVKSLPCDICKDVVTAAGDMLKDNATEEEILVYLEKTCDWLPKPNMSASCKEIVDSYLPVILDIIKGEMSRPGEVCSALNLCESLQKHLAELNHQKQLESNKIPELDMTEVVAPFMANIPLLLYPQDGPRSKPQPKDNGDVCQDCIQMVTDIQTAVRTNSTFVQALVEHVKEECDRLGPGMADICKNYISQYSEIAIQMMMHMQPKEICALVGFCDEVKEMPMQTLVPAKVASKNVIPALELVEPIKKHEVPAKSDVYCEVCEFLVKEVTKLIDNNKTEKEILDAFDKMCSKLPKSLSEECQEVVDTYGSSILSILLEEVSPELVCSMLHLCSGTRLPALTVHVTQPKDGGFCEVCKKLVGYLDRNLEKNSTKQEILAALEKGCSFLPDPYQKQCDQFVAEYEPVLIEILVEVMDPSFVCLKIGACPSAHKPLLGTEKCIWGPSYWCQNTETAAQCNAVEHCKRHVWN

    Host

    Mouse

    Reactivity

    Human

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (81.88 KDa) .

    Storage Buffer

    50 % glycerol

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — PSAP

    Entrez GeneID

    5660

    GeneBank Accession#

    BC001503

    Protein Accession#

    AAH01503

    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
  • Publication Reference
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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