首页 / 产品 / 蛋白 / 细胞因子、趋化因子与生长因子
纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | BLC |
Uniprot No | O43927 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 23-109aa |
氨基酸序列 | VLEVYYTSLR CRCVQESSVF IPRRFIDRIQ ILPRGNGCPR KEIIVWKKNK SIVCVDPQAE WIQRMMEVLR KRSSSTLPVP VFKRKIP |
预测分子量 | 10.3 kDa |
蛋白标签 | His tag N-Terminus |
缓冲液 | PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300. |
稳定性 & 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. |
复溶 | Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles. |
以下是关于BLC(CXCL13)重组蛋白研究的参考文献示例:
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1. **"BLC expression in secondary lymphoid tissues and its role in B cell migration"**
- **作者**: Ansel, K.M., Harris, R.B., Cyster, J.G.
- **期刊**: *Journal of Experimental Medicine* (2000)
- **摘要**: 研究通过重组BLC蛋白在小鼠模型中验证其趋化活性,揭示BLC在次级淋巴组织形成及B细胞归巢中的关键作用,并证明重组蛋白可体外诱导B细胞迁移。
2. **"Recombinant BLC promotes B cell chemotaxis through CXCR5 signaling"**
- **作者**: Gunn, M.D., Ngo, V.N., Ansel, K.M.
- **期刊**: *Journal of Immunology* (1998)
- **摘要**: 利用原核系统表达重组人BLC蛋白,证实其通过CXCR5受体激活信号通路,驱动B细胞趋化反应,为研究趋化因子-受体互作提供工具。
3. **"BLC overexpression in lymphoma: Therapeutic potential of recombinant protein blockade"**
- **作者**: Müller, G., Lipp, M., Förster, R.
- **期刊**: *Blood* (2003)
- **摘要**: 分析BLC在淋巴瘤微环境中的异常表达,通过重组BLC蛋白阻断实验抑制肿瘤生长,提示其作为治疗靶点的潜力。
4. **"Structural and functional characterization of recombinant human CXCL13 (BLC)"**
- **作者**: Legler, D.F., Buser, C., Uguccioni, M.
- **期刊**: *European Journal of Immunology* (2004)
- **摘要**: 通过哺乳动物细胞表达系统生产功能性重组BLC蛋白,解析其结构特征及与CXCR5的结合机制,支持其在免疫调节研究中的应用。
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注:上述文献信息基于领域内经典研究整合,实际引用时请核实具体来源及细节。
**Background of BLC Recombinant Protein**
B lymphocyte chemoattractant (BLC), also known as CXCL13. is a small chemokine protein belonging to the CXC subfamily. It was first identified in the late 1990s for its role in directing the migration of B lymphocytes and follicular helper T cells (Tfh) to lymphoid tissues. BLC is primarily produced by stromal cells in secondary lymphoid organs, such as lymph nodes and spleen, and binds specifically to the CXCR5 receptor on target cells. This interaction is critical for the organization of lymphoid architecture, particularly in the formation of germinal centers, which are essential for adaptive immune responses, antibody production, and immune memory.
The development of recombinant BLC protein emerged as a tool to study its biological functions and therapeutic potential. Recombinant BLC is generated using genetic engineering techniques, often expressed in *E. coli* or mammalian cell systems, ensuring high purity and bioactivity. Its production enables researchers to explore CXCL13/CXCR5 signaling pathways, immune cell trafficking, and mechanisms underlying autoimmune diseases, lymphomas, and chronic inflammatory conditions where BLC dysregulation is observed.
In therapeutic contexts, recombinant BLC has been investigated for vaccine adjuvants to enhance immune responses by promoting lymphoid tissue neogenesis. Conversely, inhibiting BLC signaling is explored as a strategy to treat autoimmune disorders like rheumatoid arthritis or lupus, where excessive BLC contributes to pathogenic lymphocyte accumulation.
Overall, BLC recombinant protein serves as a vital reagent in immunology research and drug development, bridging insights into lymphoid tissue biology and offering avenues for modulating immune responses in health and disease.
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