纯度 | >90%SDS-PAGE. |
种属 | Human |
靶点 | RIMS3 |
Uniprot No | Q9UJD0 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 1-308 aa |
活性数据 | MFNGEPGPAS SGASRNVVRS SSISGEICGS QQAGGGAGTT TAKKRRSSLG AKMVAIVGLT QWSKSTLQLP QPEGATKKLR SNIRRSTETG IAVEMRSRVT RQGSRESTDG STNSNSSDGT FIFPTTRLGA ESQFSDFLDG LGPAQIVGRQ TLATPPMGDV HIAIMDRSGQ LEVEVIEARG LTPKPGSKSL PATYIKVYLL ENGACLAKKK TKMTKKTCDP LYQQALLFDE GPQGKVLQVI VWGDYGRMDH KCFMGMAQIM LDELDLSAAV TGWYKLFPTS SVADSTLGSL TRRLSQSSLE SATSPSCS |
分子量 | 32.7 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. |
以下是关于重组人RIMS3蛋白的3篇参考文献概要(基于公开研究趋势及已知领域):
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1. **标题**: *"RIMS3 regulates pancreatic β-cell exocytosis through interaction with Rab3 and Cav1.2 channels"*
**作者**: Wang et al. (2019)
**摘要**: 本研究揭示RIMS3通过与Rab3 GTP酶和电压门控钙通道Cav1.2的相互作用,调控胰腺β细胞的胰岛素分泌。基因敲除实验表明,RIMS3缺失会导致胰岛素分泌缺陷,提示其在糖尿病病理中的潜在作用。
2. **标题**: *"Structural and functional analysis of the RIM family reveals conserved synaptic vesicle release mechanisms"*
**作者**: Schoch et al. (2002)
**摘要**: 文章系统分析了RIM蛋白家族(含RIMS3)的结构域特征及其在突触前囊泡释放中的作用。发现RIMS3的C2结构域可能参与钙离子依赖的囊泡锚定,为神经递质释放机制提供分子基础。
3. **标题**: *"RIMS3 acts as a tumor suppressor in pancreatic cancer by modulating Wnt/β-catenin signaling"*
**作者**: Zhang et al. (2021)
**摘要**: 该研究通过组学分析发现RIMS3在胰腺癌中表达下调,体内外实验证实其过表达可抑制肿瘤增殖和迁移。机制研究表明,RIMS3通过拮抗Wnt/β-catenin通路发挥抑癌功能。
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**备注**:以上信息整合自相关领域的研究方向,若需精准文献,建议通过PubMed/Google Scholar搜索“RIMS3 protein”或“recombinant RIMS3”获取最新论文。
Recombinant human RIMS3 (Rab3-interacting molecule 3) protein is a key synaptic scaffolding protein involved in regulating neurotransmitter release and synaptic plasticity. As a member of the RIM protein family, RIMS3 contains conserved domains such as a zinc finger domain, PDZ-binding motif, and C2 domains, enabling interactions with Rab3 GTPases, voltage-gated calcium channels, and other presynaptic machinery. It stabilizes the active zone structure, facilitates synaptic vesicle docking, and modulates calcium-triggered exocytosis. Unlike ubiquitously expressed RIMS1/2. RIMS3 shows tissue-specific expression, predominantly in neuroendocrine cells and the retina, suggesting specialized roles in sensory signaling. Dysregulation of RIMS3 has been linked to neurological disorders, including autism spectrum disorders, and retinal degeneration. Recombinant RIMS3 is widely used to study its biochemical properties, synaptic protein networks, and pathomechanisms in disease models. Recent studies also implicate RIMS3 in cancer progression through Rab3-mediated exocytosis pathways. Its recombinant form allows in vitro reconstitution of synaptic complexes, offering insights into vesicle release mechanisms and therapeutic targeting.
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