索莱宝SolarbioK113579P Anti-KCNQ1 Polyclonal AntibodyK113579Psolarbio,索莱宝-易享

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K113579P Anti-KCNQ1 Polyclonal Antibody

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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

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品牌索莱宝Solarbio

地区中国,北京,北京市

货号 K113579P

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100ul

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北京索莱宝科技有限公司

北京市通州区中关村科技园区通州园金桥科技产业基地景盛南四街15号85A三层

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北京索莱宝科技有限公司（Beijing Solarbio Science & Technology Co.,Ltd.）是一家从事生物学试剂及试剂盒的高科技生物企业。总部位于北京，并在全国设有经销或代理机构。产品因可靠而稳定的质量和完善的售后服务确立了“Solarbio”良好的品牌形象。公司秉承“以客户为中心、以产品为保障、以诚信为基础、以创新为宗旨”的发展理念，拥有专业的研发和质量检测团队以及先进的仓储和物流系统。“Solarbio”已经得到全国科研工作者的认可，成为广大经销商推崇的知名品牌。

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产品规格

品牌名称

索莱宝Solarbio

货号

K113579P

国产/进口

国产

规格

50ul,100ul

图文详情

Anti-KCNQ1 Polyclonal Antibody - 产品详情 (solarbio.com)

中文名称	KQT样亚家族钾电压门控通道成员1
宿主	Rabbit
克隆类型	Polyclonal Antibody
亚型	IgG
交叉反应	Human ; Mouse ; Rat
预测交叉反应	Pig;Cat;Rabbit
应用	WB ; IHC
稀释比例	WB 1:2000-5000. IHC 1:25-100.
靶标	KCNQ1
别名	ATFB1; ATFB3; FLJ26167; IKs producing slow voltage-gated potassium channel subunit alpha; IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1; Jervell and Lange-Nielsen syndrome 1; JLNS1; KCNA8; KCNA9; KCNQ1; KCNQ1_HUMAN; kidney and cardiac voltage dependend K+ channel; KQT-like 1; Kv1.9; Kv7.1; KVLQT1; long (electrocardiographic) QT syndrome, Ward-Romano syndrome 1; LQT; LQT1; Potassium channel, voltage-gated, shaker-relatd subfamily, member 9; Potassium voltage-gated channel subfamily KQT member 1; potassium voltage-gated channel, KQT-like subfamily, member 1; RWS; slow delayed rectifier channel subunit; SQT2; Voltage-gated potassium channel subunit Kv7.1; WRS;
背景资料	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.
Swiss Prot	P51787
Gene ID	3784
亚细胞定位	Cytoplasm Cell membrane
免疫原	Recombinant protein of human KCNQ1
Public Immunogen Range	230-550aa
理论分子量	61/75kDa
实际分子量	61kDa
纯化方法	Octanoic acid-ammonium sulfate precipitation
储存液	Buffer: PBS with 50% Glycerol, 0.03% Proclin300, 0.5% BSA, pH 7.3.
储存条件	Store at -20℃. Avoid freeze / thaw cycles.
规格	50ul ; 100ul
单位	支

以上数据均来自公开文献, Solarbio暂未进行独立验证, 仅供参考。

These protocols are for reference only. Solarbio does not independently validate these methods.

使用前请离心。如有问题请及时联系我们。

Quick spin before use. If you have any questions, please contact us.

实验图

Western blot analysis with KCNQ1 antibody diluted at 1:3000;Lane: Rat kidney.

Immunohistochemistry of paraffin-embedded Human liver cancer with KCNQ1 antibody diluted at 1:50.

实验图

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