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- 详细信息
- 文献和实验
- 技术资料
- 库存：
现询
- 供应商：
北京索莱宝科技有限公司
- 规格：
1mg/500ug/50ug/10ug
| 规格： | 1mg | 产品价格： | ￥21120.0 |
|---|---|---|---|
| 规格： | 500ug | 产品价格： | ￥14784.0 |
| 规格： | 50ug | 产品价格： | ￥2600.0 |
| 规格： | 10ug | 产品价格： | ￥988.0 |
【本资料源自公开渠道，如需（此处）屏蔽，请联系删除】
标题:Enteric glial cells aggravate the intestinal epithelial barrier damage by secreting S100汕 under high-altitude conditions
成员:Xie Huichao, Zeng Xiong, Wang Wensheng, Wang Wei, Han Ben, Tan QianShan, Hu Qiu, Liu Xingyu, Chen Shuaishuai, Chen Jun, Sun Lihua, Chen Yihui, Xiao Weidong
论文因子:4 发表期刊:Molecular Biomedicine pmid:37779161
| 基本信息 | |
| 基因名 | |
| 别名 | Protein S100-B;S-100 protein beta chain;S-100 protein subunit beta;S100 calcium-binding protein B;S100b;S100 beta;S100 calcium binding protein B |
| 外观(性状) | Lyophilized from a 0.2 μm filtered solution of 20mM PB, 150mM NaCl, pH7.4. |
| 纯度 | ≥95% as determined by reducing SDS-PAGE. |
| 储存条件 | Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8°C for 2-7 days. Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months. |
| 运输条件 | The product is shipped at 2-8°C temperature. Upon receipt, store it immediately at the temperature listed below. |
| 背景说明 | S100-B，is an acidic protein with a molecular weight of 21 kDa belonging to the S100 family.S100-B contains two EF-hand-type calcium-binding motifs separated by a hinge region with a hydrophobic cleft.S100-B plays an important role in neurodevelopment，differentiation，and brain construction.S100-B has neuroprotective effects，but at high concentrations S100-B is neurotoxic.Extracellular concentration of S100-B increases following brain damage，which easily penetrates into cerebrospinal fluid in brain damage and then into the blood.S100-B is expressed and produced by astrocytes in vertebrate brains and in the CNS，and the astrocytes are the major cells producing S100-B protein in gray matter，as well as oligodendrocytes are the predominant S100-B in protein producing cells in white matter.The major advantage of using S100-B is that elevations in serum or CSF levels provide a sensitive measure for determining CNS injury at the molecular level before gross changes develop，enabling timely delivery of crucial medical intervention before irreversible damage occurs.In addition，S100-B，which is also present in Mouse melanocytes，is a reliable marker for melanoma malignancy both in bioptic tissue and in serum. |
| 来源 | E.coli |
| 溶剂 | Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100 μg/ml. Dissolve the lyophilized protein in ddH2O. Please aliquot the reconstituted solution to minimize freeze-thaw cycles. |
| 内毒素 | Less than 0.1 ng/ug(1 IEU/ug)as determined by LAL test. |
| 单位 | 支 |
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文献和实验【本资料源自公开渠道，如需（此处）屏蔽，请联系删除】
标题:Enteric glial cells aggravate the intestinal epithelial barrier damage by secreting S100汕 under high-altitude conditions
成员:Xie Huichao, Zeng Xiong, Wang Wensheng, Wang Wei, Han Ben, Tan QianShan, Hu Qiu, Liu Xingyu, Chen Shuaishuai, Chen Jun, Sun Lihua, Chen Yihui, Xiao Weidong
论文因子:4 发表期刊:Molecular Biomedicine pmid:37779161
Characterization of Calcium Channel Binding
Figure 1.25.1 (A ) Saturation binding of [3 H]PN200‐100 to L‐type calcium channels in mouse heart membrane preparation ( n = 2). (B ) Scatchard analysis of the specific binding data: K d = 54.9 pM and B max = 116.4 fmol/mg protein
ANTIBODY BINDING TO PROTEIN A AND PROTEIN G
2c + ++ Sources of information: Akerstrom, B., Brodin, T., Reis, K., and Bjorck, L. 1985. Protein G: A powerful tool for binding and detection of monoclonal and polyclonal antibodies. J. Immunol. 135:2589-2592. Akerstrom, B. and Bjorck, L. 1986
Preparation of Recombinant Protein Spotted Arrays for Proteome‐Wide Identification of Kinase Targets
, A., Sopko, R., McCartney, R.R., Schmidt, M.C., Rachidi, N., Lee, S.J., Mah, A.S., Meng, L., Stark, M.J., Stern, D.F., De Virgilio, C., Tyers, M., Andrews, B., Gerstein, M., Schweitzer, B., Predki, P.F., and Snyder, M. 2005. Global analysis of protein
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