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MPP4 (基因名), MAGUK p55 subfamily member 4 (蛋白名), MPP4_HUMAN.
产品名称:

Human MPP4/ MAGUK p55 subfamily member 4 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 5 protein, Discs large homolog 6, ALS2CR5, DLG6

序列号:
Q96JB8
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 MPP4 Protein
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Human MPP4 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: 2q33.1 by HGNC 2q33.1 by Entrez Gene 2q33.1 by Ensembl
MPP4 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:
Interacts with MPDZ. May interact with GRIA2 (By similarity). Forms a complex with CRB1 and MPP5. Interacts with FASLG.


功能:
May play a role in retinal photoreceptors development.


亚细胞位置:
Cytoplasm Detected at the outer limiting membrane (OLM) and in the outer plexiform layer (OPL) of the retina. At the OLM, detected apical to the adherens junction (AJ).


该产品尚未在任何出版物中被引用。

[1].
"MPP5 recruits MPP4 to the CRB1 complex in photoreceptors."

[2].
"Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa."

[3].
"Cloning and characterization of the human retina-specific gene MPP4, a novel member of the p55 subfamily of MAGUK proteins."

[4].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."

[5].
"Identification of SH3 domain interaction partners of human FasL (CD178) by phage display screening."

[6].
"Membrane-associated guanylate kinase proteins MPP4 and MPP5 associate with Veli3 at distinct intercellular junctions of the neurosensory retina."

[7].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[8].
"A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2."

[9].
"Investigation of correlations between DNA methylation, suicidal behavior and aging."

[10].
"Genome-wide association for smoking cessation success: participants in the Patch in Practice trial of nicotine replacement."
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