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羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体

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产物名称: 羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体
产物型号: HSD17B4
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体  的详细介绍

羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体

规格:1尘驳/1尘濒


英文名: HSD17B4

别名: hydroxysteroid (17-beta) dehydrogenase 4; 12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase; 17 beta HSD 4; 17 beta HSD IV; 17 beta hydroxysteroid dehydrogenase 4; 17-beta-HSD 4; 17-beta-hydro

分子量: 47/80kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human HSD17B4

交叉反应:Human, Mouse, Rat, Chicken, Pig, Cow, Horse, Sheep, Guinea Pig, Zebrafish

羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体细胞定位:细胞浆 线粒体

产物介绍:background: 17Beta-HSD4 (17Beta-hydroxysteroid dehydrogenase type 4) is also known as peroxisomal multifunctional enzyme/protein 2 (MFE-2/MFP-2), D-bifunctional enzyme or 17-Beta Estradiol dehydrogenase type IV. It belongs to the 17Beta-HSD family of proteins that regulate the availability of steroids within various tissues throughout the body. 17Beta-HSD4 inactivates Estradiol through its oxidative activity but it is primarily involved in peroxisomal fatty acid and cholesterol Beta-oxidation. It has a multi-domain structure: the dehydrogenase domain is fused to a hydratase and a lipid transfer domain. 17Beta-HSD4 is a target protein of chromeceptin and it is essential for the downstream activation of Stat6. 17Beta-HSD4-deficient patients exhibit Zellweger-like syndrome and die within the first year of life. They display neuronal 羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体migration defects, facial dysmorphisms, severe hypotonia and convulsions in the neonatal period. 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. Subcellular Location: Peroxisome. Tissue Specificity: Present in many tissues with 羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体highest concentrations in liver, heart, prostate and testis. 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. Similarity: Belongs to the short-chain dehydrogenases/reductases (SDR) family. Contains 1 MaoC-like domain. Contains 1 SCP2 domain. Database links: UniProtKB/Swiss-Prot: P51659.3 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

羟基类固醇(17β)脱氢酶4/17β-贬厂顿4抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:肿瘤  心血管  细胞生物  神经生物学  信号转导  线粒体  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid



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