17β-HSD4 Polyclonal Antibody

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商品货号： PLA019065

适应性： 人,小鼠,大鼠

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

基因名称： HSD17B4
蛋白名称： Peroxisomal multifunctional enzyme type 2
Human_gene_id： 3295
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3295
Human_swiss_prot_no： P51659
Human_swiss_link： http://www.uniprot.org/uniprotkb/P51659/entry
Mouse_gene_id： 15488
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=15488
Mouse_swiss_prot_no： P51660
Mouse_swiss_link： http://www.uniprot.org/uniprot/P51660
Rat_gene_id： 79244
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=79244
Rat_swiss_prot_no： P97852
Rat_swiss_link： http://www.uniprot.org/uniprot/P97852
特异性： 17β-HSD4 Polyclonal Antibody detects endogenous levels of 17β-HSD4 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:20000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： HSD17B4; EDH17B4; Peroxisomal multifunctional enzyme type 2; MFE-2; 17-beta-hydroxysteroid dehydrogenase 4; 17-beta-HSD 4; D-bifunctional protein; DBP; Multifunctional protein 2; MPF-2
实测条带： 80kD
信号通路： Primary bile acid biosynthesis;
功能： catalytic activity:(24R,25R)-3-alpha,7-alpha,12-alpha,24-tetrahydroxy-5-beta-cholestanoyl-CoA = (24E)-3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA + H(2)O.,catalytic activity:(S)-3-hydroxyacyl-CoA + NAD(+) = 3-oxoacyl-CoA + NADH.,disease:Defects in HSD17B4 are a cause of D-bifunctional protein deficiency (DBPD) [MIM:261515]. DBPD is a disorder of peroxisomal fatty acid beta-oxidation.,function:Bifunctional enzyme acting on the peroxisomal beta-oxidation pathway for fatty acids. Catalyzes the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids.,pathway:Lipid metabolism; fatty acid beta-oxidation.,similarity:Belongs to the short-chain dehydrogenases/reductases (SDR) family.,similarity:Contains 1 SCP2 domain.,tissue specificity:Present in many tissues with highest concentrations in liver, heart, prostate and testis.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Peroxisome .
组织表达： Present in many tissues with highest concentrations in liver, heart, prostate and testis.
科研货号： PLA019065

17β-HSD4 Polyclonal Antibody

Catalog No PLA019065

Product information

基因名称： HSD17B4
蛋白名称： Peroxisomal multifunctional enzyme type 2
Human_gene_id： 3295
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3295
Human_swiss_prot_no： P51659
Human_swiss_link： http://www.uniprot.org/uniprotkb/P51659/entry
Mouse_gene_id： 15488
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=15488
Mouse_swiss_prot_no： P51660
Mouse_swiss_link： http://www.uniprot.org/uniprot/P51660
Rat_gene_id： 79244
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=79244
Rat_swiss_prot_no： P97852
Rat_swiss_link： http://www.uniprot.org/uniprot/P97852
特异性： 17β-HSD4 Polyclonal Antibody detects endogenous levels of 17β-HSD4 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:20000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： HSD17B4; EDH17B4; Peroxisomal multifunctional enzyme type 2; MFE-2; 17-beta-hydroxysteroid dehydrogenase 4; 17-beta-HSD 4; D-bifunctional protein; DBP; Multifunctional protein 2; MPF-2
实测条带： 80kD
信号通路： Primary bile acid biosynthesis;
功能： catalytic activity:(24R,25R)-3-alpha,7-alpha,12-alpha,24-tetrahydroxy-5-beta-cholestanoyl-CoA = (24E)-3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA + H(2)O.,catalytic activity:(S)-3-hydroxyacyl-CoA + NAD(+) = 3-oxoacyl-CoA + NADH.,disease:Defects in HSD17B4 are a cause of D-bifunctional protein deficiency (DBPD) [MIM:261515]. DBPD is a disorder of peroxisomal fatty acid beta-oxidation.,function:Bifunctional enzyme acting on the peroxisomal beta-oxidation pathway for fatty acids. Catalyzes the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids.,pathway:Lipid metabolism; fatty acid beta-oxidation.,similarity:Belongs to the short-chain dehydrogenases/reductases (SDR) family.,similarity:Contains 1 SCP2 domain.,tissue specificity:Present in many tissues with highest concentrations in liver, heart, prostate and testis.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Peroxisome .
组织表达： Present in many tissues with highest concentrations in liver, heart, prostate and testis.
科研货号： PLA019065

Hunan UPT Biotechnology Co.,Ltd

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