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TAZ (基因名), Tafazzin (蛋白名), taz_human.
产品名称:

Human TAZ/ Tafazzin Recombinant Protein
Tafazzin

货号:

R11108h

商标:
EIAab®
监管等级:
别名:

Protein G4.5, EFE2, G4.5

序列号:
Q16635
来源:
E.coli
种属:
Human
标签:
His
序列:
31-292aa
预估分子量:
28.82 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:
-
  • Human TAZ Protein
  • Human TAZ Protein
  • Human TAZ Protein
规格 & 价格: cart
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Human TAZ 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 TAZ Protein
The PCR product of human TAZ gene was determined by 1% Agarose stained with EB.
Human TAZ Protein
Recombinant human TAZ protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: Xq28 by HGNC Xq28 by Entrez Gene Xq28 by Ensembl
TAZ 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:
Some isoforms may be involved in cardiolipin (CL) metabolism.


亚细胞位置:
Isoform 9 Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Role of calcium-independent phospholipase A2 in the pathogenesis of Barth syndrome."

[2].
"Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism."

[3].
"Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome."

[4].
"The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies."

[5].
"A novel X-linked gene, G4.5. is responsible for Barth syndrome."

[6].
"A novel custom resequencing array for dilated cardiomyopathy."

[7].
"A novel mutation in the G4.5 (TAZ) gene in a Greek patient with Barth syndrome."

[8].
"The enigmatic role of tafazzin in cardiolipin metabolism."

[9].
"Characterization of tafazzin splice variants from humans and fruit flies."

[10].
"The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome."
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