- ￥1100 - 1980
- CUSABIO
- CN
- CSB-PA237012
- 2025年07月08日
- ELISA,WB;ELISA:1:1000-1:2000,WB:1:200-1:1000
- Rabbit
- Human,Mouse,Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Fusion protein of Human KCNQ1
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性：
/
- 标记物：
Non-conjugated
- 适应物种：
Human,Mouse,Rat
- 保质期：
6个月
- 抗原来源：
Homo sapiens (Human)
- 目录编号：
P51787
- 级别：
优
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 宿主：
Rabbit
- 应用范围：
ELISA,WB;ELISA:1:1000-1:2000,WB:1:200-1:1000
- 浓度：
>95%,Antigen affinity purification
- 靶点：
KCNQ1
- 抗体英文名：
KCNQ1 Antibody
- 抗体名：
KCNQ1;KCNA8;KCNA9;KVLQT1;Potassium voltage-gated channel subfamily KQT member 1;IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1;KQT-like 1;Voltage-gated potassium channel subunit Kv7.1
- 规格：
100μl/50μl
| 规格： | 100μl | 产品价格： | ￥1980.0 |
|---|---|---|---|
| 规格： | 50μl | 产品价格： | ￥1100.0 |
保存缓冲液
-20℃, pH7.4 PBS, 0.05% NaN3, 40% Glycerol功能
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.风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Modulation of Potassium Ion Channel Proteins Utilising Antibodies
roles within native neurones. Utilising this approach, we have investigated the role of the voltage-gated potassium channel Kv3.1b subunit within a region of the brainstem important in the regulation of autonomic function. We provide some useful control
Identification of Mutations in the Kir6.2 Subunit of the KATP Channel
The beta-cell ATP-sensitive potassium channel is a key component of stimulus —secretion coupling in the pancreatic beta-cell. The channel consists of four subunits of the inwardly rectifying potassium channel Kir6.2 and four subunits
Tissue-Specific Transgenic and Knockout Mice
KCNQ1 is a voltage-activated potassium channel α -subunit expressed in various cell types, including cardiac myocytes and epithelial cells. KCNQ1 associates with different β-subunits of the KCNE protein family. In the human heart, KCNQ1
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