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MPV17L (基因名), Mpv17-like protein (蛋白名), MP17L_HUMAN.
产品名称:

Human MPV17L/ Mpv17-like protein Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

M-LP homolog, M-LPH

序列号:
Q2QL34
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:
-
Human MPV17L Protein
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Human MPV17L Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 16p13.11 by HGNC 16p13.11 by Entrez Gene 16p13.11 by Ensembl
MPV17L 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:
Isoform 1 participates in reactive oxygen species metablism by up- or down-regulation of the genes of antioxidant enzymes.


亚细胞位置:
Isoform 1 Peroxisome membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Human Mpv17-like protein is localized in peroxisomes and regulates expression of antioxidant enzymes."

[2].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[3].
"Identification of interacting partners of Human Mpv17-like protein with a mitigating effect of mitochondrial dysfunction through mtDNA damage."

[4].
"Identification of Rhit as a novel transcriptional repressor of human Mpv17-like protein with a mitigating effect on mitochondrial dysfunction, and its transcriptional regulation by FOXD3 and GABP."

[5].
"Interactions of pathological hallmark proteins: tubulin polymerization promoting protein/p25, beta-amyloid, and alpha-synuclein."

[6].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."

[7].
"A proteome-wide perspective on peroxisome targeting signal 1(PTS1)-Pex5p affinities."

[8].
"Ubiquitin-mediated proteolysis of HuR by heat shock."

[9].
"Transcriptome analysis of human gastric cancer."

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