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TNNT1 (基因名), Troponin T, slow skeletal muscle (蛋白名), tnnt1_human.
产品名称:

Human TNNT1/ Troponin T, slow skeletal muscle Recombinant Protein
缓慢骨骼肌肌钙蛋白T

货号:

R1820h

商标:
EIAab®
监管等级:
别名:

Slow skeletal muscle troponin T, sTnT, TnTs, TNT

序列号:
P13805
来源:
E.coli
种属:
Human
标签:
His
序列:
1-154aa
预估分子量:
16.94 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:
Cancer
  • Human TNNT1 Protein
  • Human TNNT1 Protein
  • Human TNNT1 Protein
规格 & 价格: cart
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Human TNNT1 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 TNNT1 protein including hydrophilcity, hydrophobicity and antigenicity.
Human TNNT1 Protein
Recombinant human TNNT1 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 19q13.4 by HGNC 19q13.4 by Entrez Gene 19q13.4 by Ensembl
TNNT1 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].
"Close physical linkage of human troponin genes: organization, sequence, and expression of the locus encoding cardiac troponin I and slow skeletal troponin T."

[2].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[3].
"Adaptation by alternative RNA splicing of slow troponin T isoforms in type 1 but not type 2 Charcot-Marie-Tooth disease."

[4].
"Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy."

[5].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[6].
"Congenital myopathies: diseases of the actin cytoskeleton."

[7].
"A novel nemaline myopathy in the Amish caused by a mutation in troponin T1."

[8].
"A recombinant monocysteine mutant (Ser to Cys-155) of fast skeletal troponin T: identification by cross-linking of a domain involved in a physiologically relevant interaction with troponins C and I."

[9].
"A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene."

[10].
"Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) gene."
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