规格 | 价格 | 库存 |
---|---|---|
100ug | ¥ 2980.00 | 10 |
500ug | ¥ 9880.00 | 10 |
产品编号 | bs-10832P |
英文名称 | Recombinant human S100B protein, N-His |
中文名称 | 重组人S100B蛋白 |
别????名 | NEF; Protein S100 B; Protein S100-B; S 100 calcium binding protein beta chain; S 100 protein beta chain; S 100 protein beta subunit; S-100 protein beta chain; S-100 protein subunit beta; S100; S100 calcium binding protein B; S100 calcium binding protein beta (neural); S100 calcium binding protein beta chain; S100 calcium-binding protein B; S100 protein beta chain; S100B_HUMAN; S100beta; Recombinant human S100B protein, N-His??S100 β; S100-β; S100β; |
![]() | Specific References??(1)?????|?????bs-10832P has been referenced in 1 publications. [IF=3.559]?Yin X et al. Zinc?oxide?nanoparticles?ameliorate?collagen?lattice?contraction?in?human?tenon?fibroblasts. Arch Biochem Biophys.?2019 Jul 15;669:1-10.??ICC?;??Human.?? |
理论分子量 | 10kDa |
检测分子量 | 10 kDa |
性????状 | Lyophilized or Liquid |
浓????度 | >0.5 mg/ml |
物????种 | Human |
序????列 | 2-92/92 |
纯????度 | >90% as determined by SDS-PAGE |
纯化方法 | AC |
内毒素 | Not analyzed |
表达系统 | E.coli |
活性 | Not tested |
标签 | N-His |
缓?冲?液 | 10 mM TBS (pH=7.4) |
保存条件 | Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles. |
注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
产品介绍 | S100 beta is a member of the S100 family of proteins containing 2 EF-hand calcium binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however, this gene is located at 21q22.3. This protein may function in neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly. Chromosomal rearrangements and altered expression of this gene have been implicated in several neurological, neoplastic, and other types of diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes. SWISS: P04271 Gene ID: 6285 |
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