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SCN3B Protein|SCN3B蛋白质|生产厂家|技术资料

产品名称: SCN3B Protein|SCN3B蛋白质|生产厂家|技术资料
产品型号: C86-135-00
产品展商: 博飞美科
产品文档: 无相关文档

简单介绍

SCN3B Protein|SCN3B蛋白质|生产厂家|技术资料由上海创赛科学仪器有限公司品质提供,可查询SCN3B Protein价格。上海创赛科学仪器有限公司是专业**试剂生产及供应商,其优良的品质满足您不同实验的多种需求,更多产品详情请登www.canspecsci.com


SCN3B Protein|SCN3B蛋白质|生产厂家|技术资料  的详细介绍

SCN3B蛋白产品信息

别名: SCN3B, KIAA1158
表达方式: 
A DNA sequence encoding the mature form of  human SCN3B (Q9NY72) extracellular domain (Met1-Glu159) was expressed with a polyhistidine tag at the C-terminus.
种属: Human
表达宿主: Human Cells

SCN3B Protein QC Testing

纯度: > 95% as determined by SDS-PAGE SDS-PAGE
内**: < 1.0 EU per μg of the protein as determined by the LAL method
稳定性: Samples are stable for up to twelve months from date of receipt at -70℃
预测N端: Phe 23
分子量: 
The recombinant human SCN3B consists of  148 amino acids and predicts a molecular mass of 17.2 KDa. It migrates as an approximately 29 and 34 kDa due to different glycosylation.
缓冲液: Lyophilized from sterile PBS, pH 7.4.
Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
Please contact us for any concerns or special requirements.

SCN3B Protein Usage Guide

储存方法: Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

SCN3B蛋白背景综述

SCN3B (sodium channel, voltage-gated, type III, beta ,human IgG1-Fc chimera) belongs to the sodium channel auxiliary subunit SCN3B (TC 8.A.17) family. It contains 1 Ig-like C2-type (immunoglobulin-like) domain. SCN3B modulates channel gating kinetics; causes unique persistent sodium currents; inactivates the sodium channel opening more slowly than the subunit beta-1. Its association with neurofascin may target the sodium channels to the nodes of ranvier of developing axons and retain these channels at the nodes in mature myelinated axons. Defects in SCN3B are the cause of Brugada syndrome type 7. A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram. It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs (called ventricular fibrillation), the individual will faint and may die in a few minutes if the heart is not reset.

参考文献

Morgan K. et al., 2000, Proc Natl Acad Sci. 97 (5): 2308-13.
Hartley JL. et al. Genome Res. 10 (11): 1788-95.
Hirosawa M. et al., 2000, DNA Res. 6 (5): 329-36.

规格:20ug

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