KCNQ1 antibody [5E12]-单抗-深圳欣博盛生物科技有限公司

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KCNQ1 antibody [5E12]

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品牌：GeneTex

官网链接

说明书

折扣/货期

货号：GTX60528

规格：100μl

目录价：￥5800

产品详情

* 以下信息仅供参考，详情请以原厂网站为准

产品名称:

KCNQ1 antibody [5E12]

别名:

potassium voltage-gated channel subfamily Q member 1 , ATFB1 , ATFB3 , JLNS1 , KCNA8 , KCNA9 , KVLQT1 , Kv1.9 , Kv7.1 , LQT , LQT1 , RWS , SQT2 , WRS

反应种属:

Human

宿主来源:

Mouse

实验应用:

ELISA, FCM, WB

同种型:

IgG2b

免疫原:

Purified recombinant fragment of human KCNQ1 expressed in E. Coli.

克隆性:

Monoclonal

克隆号:

5000000000000

纯化方式:

Unpurified

偶联:

Unconjugated

产品浓度:

保存温度:

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

运输温度:

4°C

预期分子量:

产品形式:

Liquid

存储溶液:

Ascites, 0.03% Sodium azide.

生产商:

GeneTex

功能与背景:

This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]

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