APCS Protein (AA 17-524) (His tag)

Produktnummer ABIN7538131

Produktdetails

Target: APCS (Amyloid P Component, Serum (APCS))

Protein-Typ: Recombinant

Proteineigenschaft: AA 17-524

Spezies: Human

Quelle: Mammalian Cells

Aufreinigungstag / Konjugat: Dieses APCS Protein ist gelabelt mit His tag.

Verwendungszweck: Recombinant human SAP Protein with C-terminal 6xHis tag

Spezifität: SAP (Gly17-Asn524) 6xHis tag

Produktmerkmale: Extracellular Domain Protein

Aufreinigung: Purified from cell culture supernatant by affinity chromatography

Reinheit: The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.

Anwendungsinformationen

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Buffer: Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

Lagerung: -20 °C,-80 °C

Informationen zur Lagerung: Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

Haltbarkeit: 12 months

Antigendetails

Target: APCS (Amyloid P Component, Serum (APCS))

Andere Bezeichnung: SAP (APCS Produkte)

Synonyme: PTX2 Protein, SAP Protein, Sap Protein, APCS Protein, FP Protein, SAP(FP) Protein, apcs Protein, ptx2 Protein, sap Protein, amyloid P component, serum Protein, serum amyloid P-component Protein, amyloid P component, serum protein L homeolog Protein, APCS Protein, Apcs Protein, apcs.L Protein

Hintergrund: 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. [provided by RefSeq, Feb 2016]

Molekulargewicht: predicted molecular mass of 57.3 kDa after removal of the signal peptide. The apparent molecular mass of SAP-His is 55-70 kDa due to glycosylation.

UniProt: P07602