ARG43986

anti-PSAP antibody

anti-PSAP antibody for ELISA,Flow cytometry,ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes PSAP
Tested Reactivity Hu
Tested Application ELISA, FACS, ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Target Name PSAP
Antigen Species Human
Immunogen Human PSAP recombinant protein
Expression System E.coli
Conjugation Un-conjugated
Protein Full Name Prosaposin
Alternate Names PSAP; Prosaposin; GLBA; SAP1; Sphingolipid Activator Protein-1; Sphingolipid Activator Protein-2; Proactivator Polypeptide; Saposin-A; Saposin-B; Saposin-C; Saposin-D; SAP2; Variant Gaucher Disease And Variant Metachromatic Leukodystrophy; PARK24; PSAPD

Application Instructions

Application Suggestion
Tested Application Dilution
ELISA0.1-0.5 µg/ml
FACS1-3 µg/1x10^6
ICC/IF5 µg/ml
IHC-P2-5 µg/ml
WB0.25-0.5 µg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Buffer 0.9% NaCl, 0.2% Na2HPO4 and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.

Bioinformation

Database Links

GeneID: 5660 Human PSAP

Swiss-port # P07602 Human Prosaposin

Gene Symbol PSAP
Gene Full Name Prosaposin
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.
Function Saposin-A and saposin-C stimulate the hydrolysis of glucosylceramide by beta-glucosylceramidase (EC 3.2.1.45) and galactosylceramide by beta-galactosylceramidase (EC 3.2.1.46). Saposin-C apparently acts by combining with the enzyme and acidic lipid to form an activated complex, rather than by solubilizing the substrate.
Cellular Localization Lysosome, Secreted
Calculated MW 58 kDa
PTM Disulfide bond, Glycoprotein

Images (4) Click the Picture to Zoom In

  • ARG43986 anti-PSAP antibody IHC-P image

    Immunohistochemistry: Human thyroid papillary carcinoma stained with ARG43986 anti-PSAP antibody at 2 μg/ml dilution.

  • ARG43986 anti-PSAP antibody WB image

    Western blot: A431, Hela, HepG2 and MCF-7 stained with ARG43986 anti-PSAP antibody at 0.5 μg/mL dilution.

  • ARG43986 anti-PSAP antibody ICC/IF image

    Immunofluorescence: A549 cells stained with ARG43986 anti-PSAP antibody at 5 μg/ml dilution.

  • ARG43986 anti-PSAP antibody FACS image

    Flow Cytometry: MCF-7 cells stained with ARG43986 anti-PSAP antibody (blue) at 1 μg/1x10^6 cells dilution.