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MLPH (基因名), Melanophilin (蛋白名), melph_human.
产品名称:

Human MLPH/ Melanophilin Recombinant Protein
黑素亲和素

货号:

R13463h

商标:
EIAab®
监管等级:
别名:

Exophilin-3, Slp homolog lacking C2 domains a, Synaptotagmin-like protein 2a, SlaC2-a, SLAC2A

序列号:
Q9BV36
来源:
E.coli
种属:
Human
标签:
His
序列:
Recombinant protein
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 MLPH Protein
规格 & 价格: cart
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Human MLPH 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: 2q37.3 by HGNC 2q37.3 by Entrez Gene 2q37.3 by Ensembl
MLPH 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:
Binds RAB27A that has been activated by GTP-binding via its N-terminus. Binds MYO5A via its C-terminal coiled coil domain.


功能:
Rab effector protein involved in melanosome transport. Serves as link between melanosome-bound RAB27A and the motor protein MYO5A.


亚细胞位置:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Genome-wide association study identifies new prostate cancer susceptibility loci."

[2].
"High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts."

[3].
"In vitro reconstitution of a transport complex containing Rab27a, melanophilin and myosin Va."

[4].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[5].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[6].
"Rab27b is up-regulated in human Griscelli syndrome type II melanocytes and linked to the actin cytoskeleton via exon F-Myosin Va transcripts."

[7].
"Interactions of human Myosin Va isoforms, endogenously expressed in human melanocytes, are tightly regulated by the tail domain."

[8].
"Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)."

[9].
"Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndrome."

[10].
"A family of Rab27-binding proteins. Melanophilin links Rab27a and myosin Va function in melanosome transport."
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