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MPI (基因名), Mannose-6-phosphate isomerase (蛋白名), MPI_HUMAN.
产品名称:

Human MPI/ Mannose-6-phosphate isomerase Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Phosphohexomutase, Phosphomannose isomerase, PMI, PMI1

序列号:
P34949
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 MPI Protein
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Human MPI 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: 15q24.1 by HGNC 15q24.1 by Entrez Gene 15q24.1 by Ensembl
MPI 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:
Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.


亚细胞位置:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)."

[2].
"Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: long-term outcome and effects of mannose supplementation."

[3].
"Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib)."

[4].
"Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy."

[5].
"Purification, cDNA cloning and heterologous expression of human phosphomannose isomerase."

[6].
"Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"."

[7].
"Computational study of human phosphomannose isomerase: Insights from homology modeling and molecular dynamics simulation of enzyme bound substrate."

[8].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[9].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[10].
"Protein losing enteropathy-hepatic fibrosis syndrome in Saguenay-Lac St-Jean, Quebec is a congenital disorder of glycosylation type Ib."
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