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Prosaposin antibody (AA 17-216)

This Mouse Monoclonal antibody specifically detects Prosaposin in WB, IHC, ELISA, ICC and FACS. It exhibits reactivity toward Human and Rat.
Catalog No. ABIN7193617

Quick Overview for Prosaposin antibody (AA 17-216) (ABIN7193617)

Target

See all Prosaposin (PSAP) Antibodies
Prosaposin (PSAP)

Reactivity

  • 51
  • 22
  • 22
Human, Rat

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
  • 13
  • 12
  • 11
  • 9
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)

Clone

3B4A8
  • Binding Specificity

    • 15
    • 7
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 17-216

    Purpose

    PSAP Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human PSAP (AA: 17-216) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200-1/400

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    Prosaposin (PSAP)

    Alternative Name

    PSAP

    Background

    This gene encodes a highly conserved preproprotein that is proteolytically processed to generate four main cleavage products including 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 and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.

    Molecular Weight

    58.1 kDa

    UniProt

    P07602

    Pathways

    Positive Regulation of Endopeptidase Activity
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