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TTR (基因名), Transthyretin (蛋白名), tthy_human.
产品名称:

Human TTR/ Transthyretin Recombinant Protein
转甲状腺素蛋白

货号:

R0726h

商标:
EIAab®
监管等级:
别名:

ATTR, Prealbumin, TBPA, PALB

序列号:
P02766
来源:
E.coli
种属:
Human
标签:
His
序列:
21-147aa
预估分子量:
13.97 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:
Neurosciences
  • Human TTR Protein
  • Human TTR Protein
  • Human TTR Protein
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Human TTR 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
Human TTR Protein
The PCR product of human TTR gene was determined by 1% Agarose stained with EB.
Human TTR Protein
Recombinant human TTR protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 18q12.1 by HGNC 18q12.1 by Entrez Gene 18q12.1 by Ensembl
TTR 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:
Homotetramer. Dimer of dimers. In the homotetramer, subunits assemble around a central channel that can accommodate two ligand molecules. Interacts with RBP4.


功能:
Thyroid hormone-binding protein. Probably transports thyroxine from the bloodstream to the brain.


亚细胞位置:
Secreted Cytoplasm



[1].
"A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy."

[2].
"A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy."

[3].
"A new transthyretin mutation associated with amyloid cardiomyopathy."

[4].
"Positive association between ALDH1A2 and schizophrenia in the Chinese population."

[5].
"Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met."

[6].
"Structural and mutational analyses of protein-protein interactions between transthyretin and retinol-binding protein."

[7].
"Genetic microheterogeneity of human transthyretin detected by IEF."

[8].
"Identification of S-sulfonation and S-thiolation of a novel transthyretin Phe33Cys variant from a patient diagnosed with familial transthyretin amyloidosis."

[9].
"Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu)."

[10].
"A novel compound heterozygote (FAP ATTR Arg104His/ATTR Val30Met) with high serum transthyretin (TTR) and retinol binding protein (RBP) levels."
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