CoraLite® Plus 488-conjugated SCN5A Monoclonal antibody

SCN5A Monoclonal Antibody for FC (Intra)
Cat No. CL488-68273

产品说明书

CloneNo. 1C2B3

宿主/亚型

Mouse / IgG1

种属反应性

human, rat, rabbit

应用

FC (Intra)

Nav1.5, HH1, CMPD2, CMD1E, CDCD2

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  CoraLite® Plus 488
规格: 

-/ -


经过测试的应用

Positive FC (Intra) detected inHeLa cells
For other applications, we recommend the unconjugated version of this antibody, 68273-1-Ig

推荐稀释比

应用推荐稀释比
Flow Cytometry (FC) (INTRA)FC (INTRA) : 0.40 ug per 10^6 cells in a 100 µl suspension
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

CL488-68273 targets SCN5A in FC (Intra) applications and shows reactivity with human, rat, rabbit samples.

经测试应用 FC (Intra) Application Description
经测试反应性 human, rat, rabbit
免疫原 SCN5A fusion protein Ag19275 种属同源性预测
宿主/亚型 Mouse / IgG1
抗体类别 Monoclonal
产品类型 Antibody
全称 sodium channel, voltage-gated, type V, alpha subunit
别名 Nav1.5, HH1, CMPD2, CMD1E, CDCD2
计算分子量 2016 aa, 227 kDa
GenBank蛋白编号BC140813
基因名称 SCN5A
Gene ID (NCBI) 6331
RRIDAB_3084464
偶联类型 CoraLite® Plus 488 Fluorescent Dye
最大激发/发射波长493 nm / 522 nm
形式 Liquid
纯化方式Protein G purification
UNIPROT IDQ14524
储存缓冲液 PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA , pH 7.3
储存条件Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

Voltage-gated sodium channels are responsible for initiation and propagation of action potentials in the membranes of neurons and most electrically excitable cells (PMID: 10798388). These channels are composed of a large alpha subunit that forms the ion conduction pore and auxiliary beta subunits (PMID: 11486343). The alpha subunits form a gene family with at least 10 members. Nav1.5, encoded by the SCN5A gene in humans, is a pore forming alpha subunit of voltage-gated sodium channels. Nav1.5 is the principal Na+ channel isoform expressed in cardiomyocytes. Mutations in SCN5A gene have been linked to many cardiac electrical disorders, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus syndrome, atrial fibrillation, and dilated cardiomyopathy (PMID: 23123192).

实验方案

Product Specific Protocols
FC protocol for CL Plus 488 SCN5A antibody CL488-68273Download protocol
Standard Protocols
Click here to view our Standard Protocols
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