您好，欢迎来到试剂信息网！ [登录] [免费注册]
试剂信息网
发布求购
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。