APOA1 monoclonal antibody, clone 1405
产品名称： APOA1 monoclonal antibody, clone 1405
英文名称： APOA1 monoclonal antibody, clone 1405
产品编号： MAB4015
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 native APOA1.
- Immunogen:
- Native purified APOA1 from human plasma.
- Host:
- Mouse
- Reactivity:
- Human
- Specificity:
- Recognizes human apolipoprotein AI. No cross reactivity with Apo A-II or Apo B.
- Form:
- Liquid
- Isotype:
- IgG1
- Storage Buffer:
- In PBS, pH 7.0 (0.02% sodium azide)
- Storage Instruction:
- Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Publication Reference
- 1.
- Retrovirus-mediated expression of apolipoprotein A-I in the macrophage protects against atherosclerosis in vivo.
Ishiguro H, Yoshida H, Major AS, Zhu T, Babaev VR, Linton MF, Fazio S.J Biol Chem. 2001 Sep 28;276(39):36742-8. Epub 2001 Jul 26.
- 2.
- An inhibitor of the microsomal triglyceride transfer protein inhibits apoB secretion from HepG2 cells.
Jamil H, Gordon DA, Eustice DC, Brooks CM, Dickson JK Jr, Chen Y, Ricci B, Chu CH, Harrity TW, Ciosek CP Jr, Biller SA, Gregg RE, Wetterau JR.Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11991-5.
- Application Image
- Radioimmunoassay
- Enzyme Immunoassay
- Entrez GeneID:
- 335
- Gene Name:
- APOA1
- Gene Alias:
- MGC117399
- Gene Description:
- apolipoprotein A-I
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion, and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. [provided by RefSeq
- Other Designations:
- OTTHUMP00000069346,OTTHUMP00000069347,OTTHUMP00000069348,apolipoprotein A1
- Interactome
- Gene Pathway
- Related Disease
- Albuminuria
- Alzheimer Disease
- Alzheimer disease
- Anemia, Sickle Cell
- Anemia, sickle cell
- Angina Pectoris
- Aortic Valve Stenosis
- Atherosclerosis
- Atherosclerosis
- Brain Ischemia
- Calcinosis
- Cardiovascular Diseases
- Carotid Artery Diseases
- Cerebral Hemorrhage
- Cerebral Infarction
- Cerebrovascular Accident
- Cerebrovascular Disorders
- Chorioamnionitis
- Cleft Lip