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Mannose Phosphate Isomerase mouse mAb

商品貨號(hào)： PLA005196

適應(yīng) 性： 人,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說(shuō)明書

商品描述

發(fā)貨日期： 7
基因名稱： mpi
Human_gene_id： 4351
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4351
Human_swiss_prot_no： P34949
Human_swiss_link： http://www.uniprot.org/uniprotkb/P34949/entry
Mouse_swiss_prot_no： Q924M7
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q924M7
特異性： This antibody detects endogenous levels of Mannose Phosphate Isomerase and does not cross-react with related proteins.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Monoclonal, Mouse
稀釋： wb 1:1000 icc 1:300
純化工藝： The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： 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.
實(shí)測(cè)條帶： 54kD
信號(hào)通路： Fructose and mannose metabolism;Amino sugar and nucleotide sugar metabolism;
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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cytoplasm .
組織表達(dá)： Expressed in all tissues, but more abundant in heart, brain and skeletal muscle.
科研貨號(hào)： PLA005196

Mannose Phosphate Isomerase mouse mAb

Catalog No PLA005196

Product information

發(fā)貨日期： 7
基因名稱： mpi
Human_gene_id： 4351
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4351
Human_swiss_prot_no： P34949
Human_swiss_link： http://www.uniprot.org/uniprotkb/P34949/entry
Mouse_swiss_prot_no： Q924M7
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q924M7
特異性： This antibody detects endogenous levels of Mannose Phosphate Isomerase and does not cross-react with related proteins.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Monoclonal, Mouse
稀釋： wb 1:1000 icc 1:300
純化工藝： The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： 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.
實(shí)測(cè)條帶： 54kD
信號(hào)通路： Fructose and mannose metabolism;Amino sugar and nucleotide sugar metabolism;
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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cytoplasm .
組織表達(dá)： Expressed in all tissues, but more abundant in heart, brain and skeletal muscle.
科研貨號(hào)： PLA005196

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