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MCFD2 (基因名), Multiple coagulation factor deficiency protein 2 (蛋白名), mcfd2_human.
产品名称:

Human MCFD2/ Multiple coagulation factor deficiency protein 2 Recombinant Protein
多种凝血因子缺乏蛋白2

货号:

R15072h

商标:
EIAab®
监管等级:
别名:

Neural stem cell-derived neuronal survival protein, SDNSF

序列号:
Q8NI22
来源:
E.coli
种属:
Human
标签:
His
序列:
27-146aa
预估分子量:
13.2 kDa (monomer)
纯度:
Greater than 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 MCFD2 Protein
  • Human MCFD2 Protein
  • Human MCFD2 Protein
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Human MCFD2 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
The sequence analysis of human MCFD2 protein including hydrophilcity, hydrophobicity and antigenicity.
Human MCFD2 Protein
Recombinant human MCFD2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 2p21 by HGNC 2p21 by Entrez Gene 2p21 by Ensembl
MCFD2 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 in a calcium-dependent manner with LMAN1.


功能:
The MCFD2-LMAN1 complex forms a specific cargo receptor for the ER-to-Golgi transport of selected proteins. Plays a role in the secretion of coagulation factors.


亚细胞位置:
Endoplasmic reticulum-Golgi intermediate compartment Endoplasmic reticulum Golgi apparatus


该产品尚未在任何出版物中被引用。

[1].
"Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex."

[2].
"Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII."

[3].
"New insights into multiple coagulation factor deficiency from the solution structure of human MCFD2."

[4].
"The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene."

[5].
"Genotype-phenotype correlation in combined deficiency of factor V and factor VIII."

[6].
"Structural basis for the cooperative interplay between the two causative gene products of combined factor V and factor VIII deficiency."

[7].
"EF-hand domains of MCFD2 mediate interactions with both LMAN1 and coagulation factor V or VIII."

[8].
"The sugar-binding ability of ERGIC-53 is enhanced by its interaction with MCFD2."

[9].
"Novel germ cell markers characterize testicular seminoma and fetal testis."

[10].
"Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India."
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