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Prosaposin Protein (PSAP) (His tag)

Recombinant Prosaposin protein expressed in HEK-293 Cells.
Catalog No. ABIN7317152

Quick Overview for Prosaposin Protein (PSAP) (His tag) (ABIN7317152)

Target

See all Prosaposin (PSAP) Proteins
Prosaposin (PSAP)

Protein Type

Recombinant

Origin

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Human

Source

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HEK-293 Cells

Purity

> (79.8+19.7) % as determined by reducing SDS-PAGE..
  • Purification tag / Conjugate

    This Prosaposin protein is labelled with His tag.

    Purpose

    Recombinant Human PSAP/Prosaposin Protein (His Tag)

    Sequence

    Met 1-Asn524

    Characteristics

    A DNA sequence encoding the human PSAP (NP_002769.1) (Met1-Asn524) was expressed with a polyhistidine tag at the C-terminus.

    Endotoxin Level

    < 1.0 EU per μg of the protein as determined by the LAL method.
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from sterile PBS, pH 7.4

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Target

    Prosaposin (PSAP)

    Alternative Name

    PSAP/Prosaposin

    Background

    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.

    Synonym: GLBA,SAP1

    Molecular Weight

    57.9 kDa

    NCBI Accession

    NP_002769

    Pathways

    Positive Regulation of Endopeptidase Activity
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