HSD17B10 purified MaxPab rabbit polyclonal antibody (D01P)
产品名称： HSD17B10 purified MaxPab rabbit polyclonal antibody (D01P)
英文名称： HSD17B10 purified MaxPab rabbit polyclonal antibody (D01P)
产品编号： H00003028-D01P
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Rabbit polyclonal antibody raised against a full-length human HSD17B10 protein.
- Immunogen:
- HSD17B10 (NP_004484.1, 1 a.a. ~ 261 a.a) full-length human protein.
- Sequence:
- MAAACRSVKGLVAVITGGASGLGLATAERLVGQGASAVLLDLPNSGGEAQAKKLGNNCVFAPADVTSEKDVQTALALAKGKFGRVDVAVNCAGIAVASKTYNLKKGQTHTLEDFQRVLDVNLMGTFNVIRLVAGEMGQNEPDQGGQRGVIINTASVAAFEGQVGQAAYSASKGGIVGMTLPIARDLAPIGIRVMTIAPGLFGTPLLTSLPEKVCNFLASQVPFPSRLGDPAEYAHLVQAIIENPFLNGEVIRLDGAIRMQP
- Host:
- Rabbit
- Reactivity:
- Human
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- MSDS:
Download
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of HSD17B10 expression in transfected 293T cell line (H00003028-T02) by HSD17B10 MaxPab polyclonal antibody.
Lane 1: HSD17B10 transfected lysate(26.90 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 3028
- GeneBank Accession#:
- NM_004493.2
- Protein Accession#:
- NP_004484.1
- Gene Name:
- HSD17B10
- Gene Alias:
- 17b-HSD10,ABAD,CAMR,DUPXp11.22,ERAB,HADH2,HCD2,MHBD,MRPP2,MRX17,MRX31,MRXS10,SCHAD,SDR5C1
- Gene Description:
- hydroxysteroid (17-beta) dehydrogenase 10
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq
- Other Designations:
- 17-beta-hydroxysteroid dehydrogenase type 10,3-hydroxy-2-methylbutyryl-CoA dehydrogenase,AB-binding alcohol dehydrogenase,OTTHUMP00000023348,OTTHUMP00000023349,amyloid-beta binding polypeptide,amyloid-beta peptide binding alcohol dehydrogenase,mental reta