TNNI3 polyclonal antibody (A01)
产品名称: TNNI3 polyclonal antibody (A01)
英文名称: TNNI3 polyclonal antibody (A01)
产品编号: H00007137-A01
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 polyclonal antibody raised against a partial recombinant TNNI3.
- Immunogen:
- TNNI3 (NP_000354, 102 a.a. ~ 210 a.a) partial recombinant protein with GST tag.
- Sequence:
- ARVDKVDEERYDIEAKVTKNITEIADLTQKIFDLRGKFKRPTLRRVRISADAMMQALLGARAKESLDLRAHLKQVKKEDTEKENREVGDWRKNIDALSGMEGRKKKFES
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- 50 % glycerol
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (38.1 KDa) .
- MSDS:
- Download
- Applications
- Western Blot (Tissue lysate)
- TNNI3 polyclonal antibody (A01), Lot # 060110JC01. Western Blot analysis of TNNI3 expression in human ovarian cancer.
- Protocol Download
- Western Blot (Recombinant protein)
- Protocol Download
- Entrez GeneID:
- 7137
- GeneBank Accession#:
- NM_000363
- Protein Accession#:
- NP_000354
- Gene Name:
- TNNI3
- Gene Alias:
- CMD2A,CMH7,MGC116817,RCM1,TNNC1,cTnI
- Gene Description:
- troponin I type 3 (cardiac)
- Gene Ontology:
- Hyperlink
- Gene Summary:
- Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. This gene encodes the TnI-cardiac protein and is exclusively expressed in cardiac muscle tissues. Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM). [provided by RefSeq
- Other Designations:
- familial hypertrophic cardiomyopathy 7,troponin I, cardiac
- Related Disease
- Alzheimer Disease
- Alzheimer disease
- Cardiomegaly
- Cardiomyopathy, Dilated
- Cardiomyopathy, Hypertrophic
- Cardiomyopathy, Hypertrophic, Familial
- Cardiomyopathy, Restrictive
- Cardiovascular Diseases
- Death, Sudden, Cardiac
- Diabetes Complications
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Hypertrophy, Left Ventricular
- Lipid Metabolism, Inborn Errors
- Metabolic Syndrome X
- Mitochondrial Myopathies
- Neoplasms
- Osteoporosis
- Tachycardia, Ventricular