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ALG1 rabbit pAb

商品貨號： PLA020440

適應(yīng) 性： 人,小鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： ALG1 HMAT1 HMT1 PSEC0061 UNQ861/PRO1870
蛋白名稱： ALG1
Human_gene_id： 56052
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=56052
Human_swiss_prot_no： Q9BT22
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9BT22/entry
Mouse_gene_id： 208211
Mouse_gene_link： https://www.uniprot.org/uniprot/208211
Mouse_swiss_prot_no： Q921Q3
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q921Q3
特異性： This antibody detects endogenous levels of ALG1 at Human/Mouse
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1：500-2000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
分子量： 51kD
功能： catalytic activity:GDP-mannose + chitobiosyldiphosphodolichol = GDP + beta-1,4-D-mannosylchitobiosyldiphosphodolichol.,disease:Defects in ALG1 are the cause of congenital disorder of glycosylation type 1K (CDG1K) [MIM:608540]. CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.,function:Participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. Involved in assembling the dolichol-pyrophosphate-GlcNAc(2)-Man(5) intermediate on the cytoplasmic surface of the ER.,online information:GlycoGene database,pathway:Protein modification; protein glycosylation.,similarity:Belongs to the glycosyltransferase 1 family.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Endoplasmic reticulum membrane ; Single-pass type II membrane protein .
科研貨號： PLA020440

ALG1 rabbit pAb

Catalog No PLA020440

Product information

基因名稱： ALG1 HMAT1 HMT1 PSEC0061 UNQ861/PRO1870
蛋白名稱： ALG1
Human_gene_id： 56052
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=56052
Human_swiss_prot_no： Q9BT22
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9BT22/entry
Mouse_gene_id： 208211
Mouse_gene_link： https://www.uniprot.org/uniprot/208211
Mouse_swiss_prot_no： Q921Q3
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q921Q3
特異性： This antibody detects endogenous levels of ALG1 at Human/Mouse
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1：500-2000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
分子量： 51kD
功能： catalytic activity:GDP-mannose + chitobiosyldiphosphodolichol = GDP + beta-1,4-D-mannosylchitobiosyldiphosphodolichol.,disease:Defects in ALG1 are the cause of congenital disorder of glycosylation type 1K (CDG1K) [MIM:608540]. CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.,function:Participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. Involved in assembling the dolichol-pyrophosphate-GlcNAc(2)-Man(5) intermediate on the cytoplasmic surface of the ER.,online information:GlycoGene database,pathway:Protein modification; protein glycosylation.,similarity:Belongs to the glycosyltransferase 1 family.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Endoplasmic reticulum membrane ; Single-pass type II membrane protein .
科研貨號： PLA020440

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

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