R&D Systems代理5536-SK-010 Recombinant Human Sphingosine Kinase 1/SPHK1 Protein, CF (10 UG)

2025-06-25

货号:5536-SK-010

品牌:R&D Systems

规格:10ug

目录价:¥4490.00

市场价格:¥3592.00

会员价格:¥3592.00

  • 到货时间:3~4周

    金山科研平台,产品价格货期咨询微信:jinshanbio Source:Spodoptera frugiperda, Sf 21 (baculovirus)-derived, Asp2-Leu398 with an N-terminal Met and 6-His tag Accession #:NP_068807 N-terminal Sequence Analysis:Inconclusive result, Met predicted. Protein identity confirmed by MS analysis of tryptic fragments. Purity:>75%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain at 5 µg per lane. Endotoxin Level: Predicted Molecular Mass:45kDa SDS-PAGE:40-43 kDa, reducing conditions Activity:Measured by its ability to phosphorylate Omega-(7-nitro-2-1,3-benzoxadiazol-4-yl)-D-erythro-sphingosine (NBD-sphingosine).The specific activity is >200 pmol/min/µg, as measured under the described conditions. Formulation:Supplied as a 0.2 µm filtered solution in MES, NaCl, Glycerol and DTT.See Certificate of Analysis for details. Molecule Information: Sphingosine Kinase 1/SPHK1 Aliases: SK1; SPK1 Entrez Gene IDs: 8877 (Human); 20698 (Mouse); 170897 (Rat) Background: SPHK1 Sphingosine kinases are cytosolic or membrane-associated enzymes that catalyze the phosphorylation of sphingosine to sphingosine-1-phosphate (S1P). Two types of sphingosine kinases, SPHK1 and SPHK2, are known to be expressed in human cells. The two enzymes share considerable amino acid sequence similarity, but differ in their N-terminal and central regions. The two proteins also differ in tissue distribution and some kinetic properties. S1P is a lipid messenger that regulates diverse physiological processes including cell proliferation, migration, apoptosis, inflammation, calcium homeostasis and cytoskeletal structure. The level of S1P is tightly controlled by SPHKs and S1P degrading enzymes. SPHK1 and its activation can be stimulated by several growth factors such as tumor necrosis factor-alpha, epidermal growth factor and transforming growth factor-beta. Expression of SPHK1 has been found to increase in many human solid tumors and overexpression of SPHK1 is associated with tumor angiogenesis. Such studies have implicated SPHK1 as a new target for cancer treatment.

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