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安全信息

SAB5200036

Sigma-Aldrich

Monoclonal Anti-KCNT1 antibody produced in mouse

clone S3-26, 1 mg/mL, purified immunoglobulin

别名:

Anti-SLACK potassium channel, S3-26, Anti-potassium channel, subfamily T, member 1

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

mouse

质量水平

偶联物

unconjugated

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

S3-26, monoclonal

表单

buffered aqueous glycerol solution

分子量

antigen predicted mol wt 140 kDa

种属反应性

rat, human (weak), mouse

浓度

1 mg/mL

技术

immunohistochemistry: suitable
western blot: suitable

同位素/亚型

IgG1

NCBI登记号

UniProt登记号

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

相关类别

特异性

Detects ~140 kDa.

免疫原

Fusion protein amino acids 1168-1237 of rat Slo2.2 (Slack); NP_068625

特点和优势

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

外形

Solution in PBS, pH 7.4, 50% glycerol, and 0.09% sodium azide

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Duyen H Pham et al.
Human molecular genetics, 26(11), 2042-2052 (2017-03-24)
De novo and inherited mutations of X-chromosome cell adhesion molecule protocadherin 19 (PCDH19) cause frequent, highly variable epilepsy, autism, cognitive decline and behavioural problems syndrome. Intriguingly, hemizygous null males are not affected while heterozygous females are, contradicting established X-chromosome inheritance.

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