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HPRT Monoclonal Antibody

商品貨號： PLA004851

適應(yīng) 性： 人

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

發(fā)貨日期： 7
基因名稱： HPRT1
蛋白名稱： Hypoxanthine-guanine phosphoribosyltransferase
Human_gene_id： 3251
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3251
Human_swiss_prot_no： P00492
Human_swiss_link： http://www.uniprot.org/uniprotkb/P00492/entry
Mouse_swiss_prot_no： P00493
Mouse_swiss_link： http://www.uniprot.org/uniprot/P00493
特異性： HPRT Monoclonal Antibody detects endogenous levels of HPRT protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： HPRT1; HPRT; Hypoxanthine-guanine phosphoribosyltransferase; HGPRT; HGPRTase
信號通路： Purine metabolism;Drug metabolism;
功能： catalytic activity:GMP + diphosphate = guanine + 5-phospho-alpha-D-ribose 1-diphosphate.,catalytic activity:IMP + diphosphate = hypoxanthine + 5-phospho-alpha-D-ribose 1-diphosphate.,cofactor:Binds 2 magnesium ions per subunit. One of the ions does not make direct protein contacts.,disease:Defects in HPRT1 are the cause of gout [MIM:300323]; also known as HPRT-related gout or Kelley-Seegmiller syndrome. Gout is characterized by partial enzyme activity and hyperuricemia.,disease:Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:300322]. LNS is characterized by complete lack of enzymatic activity that results in hyperuricemia, choreoathetosis, mental retardation, and compulsive self-mutilation.,online information:Hypoxanthine-guanine phosphoribosyltransferase entry,pathway:Purine metabolism; IMP biosynthesis via salvage pathway; IMP from hypoxanthine: step 1/1.,similarity:Belongs to the purine/pyrimidine phosphoribosyltransferase family.,subunit:Homotetramer.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cytoplasm.
組織表達(dá)： Brain,
科研貨號： PLA004851

HPRT Monoclonal Antibody

Catalog No PLA004851

Product information

發(fā)貨日期： 7
基因名稱： HPRT1
蛋白名稱： Hypoxanthine-guanine phosphoribosyltransferase
Human_gene_id： 3251
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3251
Human_swiss_prot_no： P00492
Human_swiss_link： http://www.uniprot.org/uniprotkb/P00492/entry
Mouse_swiss_prot_no： P00493
Mouse_swiss_link： http://www.uniprot.org/uniprot/P00493
特異性： HPRT Monoclonal Antibody detects endogenous levels of HPRT protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： HPRT1; HPRT; Hypoxanthine-guanine phosphoribosyltransferase; HGPRT; HGPRTase
信號通路： Purine metabolism;Drug metabolism;
功能： catalytic activity:GMP + diphosphate = guanine + 5-phospho-alpha-D-ribose 1-diphosphate.,catalytic activity:IMP + diphosphate = hypoxanthine + 5-phospho-alpha-D-ribose 1-diphosphate.,cofactor:Binds 2 magnesium ions per subunit. One of the ions does not make direct protein contacts.,disease:Defects in HPRT1 are the cause of gout [MIM:300323]; also known as HPRT-related gout or Kelley-Seegmiller syndrome. Gout is characterized by partial enzyme activity and hyperuricemia.,disease:Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:300322]. LNS is characterized by complete lack of enzymatic activity that results in hyperuricemia, choreoathetosis, mental retardation, and compulsive self-mutilation.,online information:Hypoxanthine-guanine phosphoribosyltransferase entry,pathway:Purine metabolism; IMP biosynthesis via salvage pathway; IMP from hypoxanthine: step 1/1.,similarity:Belongs to the purine/pyrimidine phosphoribosyltransferase family.,subunit:Homotetramer.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cytoplasm.
組織表達(dá)： Brain,
科研貨號： PLA004851

Hunan UPT Biotechnology Co.,Ltd

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E-mail：service@uptbio.com

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