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TNNT2 (基因名), Troponin T, cardiac muscle (蛋白名), tnnt2_human.
产品名称:

Human TNNT2/ Troponin T, cardiac muscle Recombinant Protein
心肌肌钙蛋白T

货号:

R1339h

商标:
EIAab®
监管等级:
别名:

Cardiac muscle troponin T, cTnT, TnTc

序列号:
P45379
来源:
E.coli
种属:
Human
标签:
His
序列:
10-179aa
预估分子量:
18.7 kDa (monomer)
纯度:
Greater than 95% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Signal Transduction
  • Human TNNT2 Protein
  • Human TNNT2 Protein
  • Human TNNT2 Protein
规格 & 价格: cart
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Human TNNT2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
The sequence analysis of human TNNT2 protein including hydrophilcity, hydrophobicity and antigenicity.
Human TNNT2 Protein
Recombinant human TNNT2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 1q32.1 by HGNC 1q32.1 by Entrez Gene 1q32.1 by Ensembl
TNNT2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Troponin T is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene."

[2].
"Mutations profile in Chinese patients with hypertrophic cardiomyopathy."

[3].
"A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy."

[4].
"Human cardiac troponin T: identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q."

[5].
"[Study of mutations causing hypertrophic cardiomyopathy in a group of patients from Espirito Santo, Brazil]."

[6].
"[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy]."

[7].
"The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy."

[8].
"Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy."

[9].
"[Association of TNNT2 gene mutations with idiopathic dilated cardiomyopathy in a Chengdu population]."

[10].
"Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients."
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