您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > 羟基类固醇(17β)脱氢酶4/17β-HSD4抗体
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
羟基类固醇(17β)脱氢酶4/17β-HSD4抗体
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。

产品名称
Anti-HSD17B4
Anti-hydroxysteroid 17-beta dehydrogenase 4 Antibody
产品介绍
靶标:

HSD17B4


产品别名:

DBP; MFE-2; MFP-2; MPF-2; PRLTS1; SDR8C1; HSD17B4; hydroxysteroid 17-beta dehydrogenase 4; hydroxysteroid 17-beta dehydrogenase 4; peroxisomal multifunctional enzyme type 2; 17-beta-HSD 4; 17-beta-HSD IV; 17-beta-hydroxysteroid dehydrogenase 4; 17beta-estradiol dehydrogenase type IV; 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase; D-3-hydroxyacyl-CoA dehydratase; D-bifunctional protein, peroxisomal; beta-hydroxyacyl dehydrogenase; beta-keto-reductase; epididymis secretory sperm binding protein; hydroxysteroid dehydrogenase 4; multifunctional protein 2; peroxisomal multifunctional protein 2; short chain dehydrogenase/reductase family 8C member 1; 羟基类固醇(17β)脱氢酶4/17β-HSD4;


背景信息:
hydroxysteroid 17-beta dehydrogenase 4(HSD17B4) Homo sapiens The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014],

宿主:Rbt
类型:Pab
同种型:IgG  
应用:WB
纯化方式:亲和纯化
偶联物:Unconjugated
性状:液体
存储溶液:参阅说明书
浓度:Batch dependent (Please refer to the vial label for the specific concentration.)
稀释比例: Optimal dilutions/concentrations should be determined by the end user           
储存:经常使用则4°C保存。-20°C保存不超过两年。避免反复冻融。
注意事项:仅供实验室使用。不适用于人类或动物的任何临床,治疗或诊断用途。不适合动物或人类食用。