- ¥1 - 3980
- PEPROTECH
- 中国/美国
- xy-020Ra01
- 2025年08月26日
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- 文献和实验
- 技术资料
- 保存条件：
-20℃
- 保质期：
12个月
- 英文名：
Recombinant S100 Calcium Binding Protein A4 (S100A4)
- 库存：
1000
- 供应商：
上海信裕
| Organism species | Rattus norvegicus (Rat) |
| Product No. | xy020Ra01 |
| Source | Prokaryotic expression |
| Host | E.coli |
| Purity | > 95% |
| UOM | 50ug |
| Predicted Molecular Mass | n/a |
| Concentration | n/a |
| Applications | SDS-PAGE; WB; ELISA; IP. |
| Endotoxin Level | <1.0EU per 1µg (determined by the LAL method) |
| Formulation | Supplied as lyophilized form in PBS, pH7.4, containing 5% trehalose, 0.01% sarcosyl. |
Stability Test: The thermal stability is described by the loss rate of the target protein. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37oC for 48h, and no obvious degradation and precipitation were observed. (Referring from China Biological Products Standard, which was calculated by the Arrhenius equation.) The loss of this protein is less than 5% within the expiration date under appropriate storage condition.
Protein bands: 10kDa, 14kDa, 18kDa, 22kDa, 26kDa, 33kDa, 44kDa and 70kDa.
Double intensity bands: The 26kDa, 18kDa, 10kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy.
S100钙结合蛋白A4(S100A4)重组蛋白Ready-to-use: No need to heat, dilute or add reducing agents before use.
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文献和实验Characterization of Epithelial Cells in the Hair Follicle With S100 Proteins
proteins are expressed in very restricted regions of the hair follicle: S100A3 and S100A6 in distinct postmitotic differentiated epithelial cells and S100A4 and S100A6 in the epithelial stem cell compartments. Characterization of epithelial cells
CUSABIO季度文献盘点：二季度新增600篇产品引用文献，总文献数量已达 31400篇！
calcium binding protein A8 (S100A8) ELISA kit; CSB-EL020641MOMouse Protein S100-A9(S100A9) ELISA kit; CSB-EL020642MO 研究亮点 研究发现SFTSV可感染雄性小鼠生殖道（睾丸、附睾等），靶向间质细胞诱导凋亡和焦亡，降低睾酮水平并损害精子发生。单细胞测序揭示CCR2⁺/SPP1⁺巨噬细胞浸润驱动附睾炎症和纤维化，S100A4抑制剂氯硝柳胺可减轻病理损伤并降低死亡率。动物实验提示潜在性传播风险
/EBPβ.J Hepatol, 2026 Jun 18 图源：10.1016/j.jhep.2026.05.025[7] 中国科学院上海药物研究所何勇研究员团队联合吉林大学第一医院高沿航教授团队，近期在Journal of Hepatology发表了一篇研究。该研究揭示了对乙酰氨基酚（APAP）诱导急性肝损伤早期炎症调控的新机制，阐明了新型抗炎因子IL-19在选择性抑制S100A8/A9促炎型巨噬细胞浸润中的关键作用。研究团队通过构建多种基因敲除小鼠模型并结合单细胞测序等技术发现，IL
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