STAR monoclonal antibody (M01A), clone 5F9
产品名称: STAR monoclonal antibody (M01A), clone 5F9
英文名称: STAR monoclonal antibody (M01A), clone 5F9
产品编号: H00006770-M01A
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:
- Mouse monoclonal antibody raised against a partial recombinant STAR.
- Immunogen:
- STAR (AAH10550, 81 a.a. ~ 180 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- EAMQKALGILSNQEGWKKESQQDNGDKVMSKVVPDVGKVFRLEVVVDQPMERLYEELVERMEAMGEWNPNVKEIKVLQKIGKDTFITHELAAEAAGNLVG
- Host:
- Mouse
- Reactivity:
- Human
- Isotype:
- IgG2a Kappa
- Storage Buffer:
- In ascites fluid
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (36.63 KDa) .
- MSDS:
- Download
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of STAR expression in transfected 293T cell line by STAR monoclonal antibody (M01A), clone 5F9.
Lane 1: STAR transfected lysate(31.9 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Western Blot (Recombinant protein)
- Protocol Download
- Application Image
- Western Blot (Transfected lysate)
- enlarge
- Western Blot (Recombinant protein)
- ELISA
- Entrez GeneID:
- 6770
- GeneBank Accession#:
- BC010550
- Protein Accession#:
- AAH10550
- Gene Name:
- STAR
- Gene Alias:
- STARD1
- Gene Description:
- steroidogenic acute regulatory protein
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene plays a key role in the acute regulation of steroid hormone synthesis by enhancing the conversion of cholesterol into pregnenolone. This protein permits the cleavage of cholesterol into pregnenolone by mediating the transport of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided by RefSeq
- Other Designations:
- START domain containing 1,StAR-related lipid transfer (START) domain containing 1,cholesterol trafficker,mitochondrial steroid acute regulatory protein,steroid acute regulatory protein,steroidogenic acute regulator
- Related Disease
- Addison Disease
- Alzheimer Disease
- Alzheimer disease
- Cardiovascular Diseases
- Diabetes Mellitus, Type 2
- Edema
- Endometrial Neoplasms
- Genetic Predisposition to Disease
- Kidney Failure, Chronic
- Lymphoma, Non-Hodgkin
- Obesity
- Ovarian Failure, Premature
- Polycystic Ovary Syndrome
- Puberty, Delayed
- Puberty, Precocious
- Thrombophilia
- Tobacco Use Disorder