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Mannose Phosphate Isomerase Mouse mAb

-YM1237

2
主要信息
Target

Mannose Phosphate Isomerase

Host Species

Mouse

Reactivity

Human, Rat

Applications

WB, ICC

MW

54kD (Observed)

Conjugate/Modification

Unmodified

货号: YM1237
规格
价格
货期
数量
200μL
¥3,780.00
一周

0

100μL
¥2,300.00
一周

0

40μL
¥960.00
一周

0

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详细信息
推荐稀释比
WB 1:1000; ICC 1:300
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
This antibody detects endogenous levels of Mannose Phosphate Isomerase and does not cross-react with related proteins.
纯化工艺
The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
实测条带
54kD
修饰
Unmodified
克隆性
Monoclonal
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抗原&靶点信息
免疫原:
Purified recombinant human Mannose Phosphate Isomerase protein fragments expressed in E.coli.
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特异性:
This antibody detects endogenous levels of Mannose Phosphate Isomerase and does not cross-react with related proteins.
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基因名称:
mpi
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别名:
PMI1 ;
CDG1B ;
FLJ39201 ;
Mannose 6 phosphate isomerase ;
Mannose-6-phosphate isomerase ;
MANNOSEPHOSPHATE ISOMERASE ;
MGC94106 ;
MPI ;
MPI_HUMAN ;
Phosphohexomutase ;
phosphomannose isomerase 1 ;
Phosphomannose isomerase ;
PMI ;
PMI1.
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数据库链接:
Organism 基因 ID SwissProt
Human 4351; P34949;
Mouse Q924M7;
背景:
Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014],
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功能:
Catalytic activity:D-mannose 6-phosphate = D-fructose 6-phosphate.,cofactor:Binds 1 zinc ion per subunit.,Disease:Defects in MPI are the cause of congenital disorder of glycosylation type 1B (CDG1B) [MIM:602579]; also known as carbohydrate-deficient glycoprotein syndrome type Ib (CDGS1B). Congenital disorders of glycosylation are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. They are characterized by under-glycosylated serum glycoproteins. CDG1B is clinically characterized by protein-losing enteropathy.,Function:Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.,pathway:Nucleotide-sugar biosynthesis; GDP-D-mannose biosynthesis; alpha-D-mannose 1-phosphate from D-fructose 6-phosphate: step 1/2.,similarity:Belongs to the mannose-6-phosphate isomerase type 1 family.,tissue specificity:Expressed in all tissues, but more abundant in heart, brain and skeletal muscle.,
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细胞定位:
Cytoplasm .
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组织表达:
Expressed in all tissues, but more abundant in heart, brain and skeletal muscle.
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研究领域:
>>Fructose and mannose metabolism ;
>>Amino sugar and nucleotide sugar metabolism ;
>>Metabolic pathways ;
>>Biosynthesis of cofactors ;
>>Biosynthesis of nucleotide sugars
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货号: YM1237
规格
价格
货期
数量
200μL
¥3,780.00
一周

0

100μL
¥2,300.00
一周

0

40μL
¥960.00
一周

0

加入购物车

已收藏

收藏

定制服务咨询

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