KCNE1 monoclonal antibody (M13), clone 2A6
产品名称： KCNE1 monoclonal antibody (M13), clone 2A6
英文名称： KCNE1 monoclonal antibody (M13), clone 2A6
产品编号： H00003753-M13
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse monoclonal antibody raised against a full length recombinant KCNE1.
- Immunogen:
- KCNE1 (AAH36452, 1 a.a. ~ 105 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- MILSNTTAVTPFLTKLWQETVQQGGNMSGLAHRSPRSGDGKLEALYVLMVLGFFGFFTLGIMLSYIRSKKLEHSNDPFNVYIESDAWQEKDKAYVQARVLESYRS
- Host:
- Mouse
- Reactivity:
- Human
- Isotype:
- IgG2a Kappa
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
- MSDS:
Download
- Applications
- Immunoprecipitation
- Immunoprecipitation of KCNE1 transfected lysate using anti-KCNE1 monoclonal antibody and Protein A Magnetic Bead (U0007), and immunoblotted with KCNE1 MaxPab rabbit polyclonal antibody.
- Protocol Download
- Sandwich ELISA (Recombinant protein)
- Detection limit for recombinant GST tagged KCNE1 is approximately 3ng/ml as a capture antibody.
- Protocol Download
- Entrez GeneID:
- 3753
- GeneBank Accession#:
- BC036452
- Protein Accession#:
- AAH36452
- Gene Name:
- KCNE1
- Gene Alias:
- FLJ18426,FLJ38123,FLJ94103,ISK,JLNS,JLNS2,LQT2/5,LQT5,MGC33114,MinK
- Gene Description:
- potassium voltage-gated channel, Isk-related family, member 1
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq
- Other Designations:
- IKs producing slow voltage-gated potassium channel subunit beta Mink,OTTHUMP00000108623,OTTHUMP00000108625,OTTHUMP00000108626,cardiac delayed rectifier potassium channel protein,delayed rectifier potassium channel subunit IsK,minimal potassium channel,pot
- Related Disease
- Arrhythmia
- Arrhythmias, Cardiac
- Atrial Fibrillation
- Atrioventricular Block
- Brugada Syndrome
- Cardiomyopathies
- Cardiovascular Diseases
- Channelopathies
- Chromosome Deletion
- Cognition
- Death, Sudden
- Death, Sudden, Cardiac
- Diabetes Mellitus, Type 2
- Edema
- Gastroparesis
- Genetic Predisposition to Disease
- Hearing Loss
- Hearing Loss, Noise-Induced
- Heart Arrest