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HADHB (基因名), Trifunctional enzyme subunit beta, mitochondrial (蛋白名), echb_human.
产品名称:

Human HADHB/ Trifunctional enzyme subunit beta, mitochondrial Recombinant Protein
线粒体三功能酶亚基β

货号:

R14272h

商标:
EIAab®
监管等级:
别名:

TP-beta, MSTP029

序列号:
P55084
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% 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:
Cardiovascular
Human HADHB Protein
规格 & 价格: cart
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Human HADHB 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
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 2p23.3 by HGNC 2p23.3 by Entrez Gene 2p23.3 by Ensembl
HADHB 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:
Octamer of 4 alpha (HADHA) and 4 beta (HADHB) subunits. Interacts with RSAD2/viperin.


功能:
N/A


亚细胞位置:
Mitochondrion Mitochondrion inner membrane Mitochondrion outer membrane Endoplasmic reticulum


该产品尚未在任何出版物中被引用。

[1].
"Fluorescence in situ hybridization mapping of the alpha and beta subunits (HADHA and HADHB) of human mitochondrial fatty acid beta-oxidation multienzyme complex to 2p23 and their evolution."

[2].
"Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency."

[3].
"Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunits."

[4].
"Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients."

[5].
"Human cytomegalovirus directly induces the antiviral protein viperin to enhance infectivity."

[6].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[7].
"Clinical and molecular aspects of Japanese patients with mitochondrial trifunctional protein deficiency."

[8].
"Generation and annotation of the DNA sequences of human chromosomes 2 and 4."

[9].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[10].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
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