Anti-CFI Antibody |产品详情|进口榴莲视频官网成人采购网

您好，欢迎来到榴莲视频成版APP下载生物网站！请登录注册

我的订单 | 联系榴莲视频成版APP下载 | 在线客服QQ：3012681483 | 客服电话：400-968-7988 | 工作时间：08:30-17:30

主营产品： ELISA榴莲视频网站入口、抗体、补体血清、兔补体、干扰素、小鼠测温仪、进口榴莲视频官网成人、Quidel代理、Swant代理、PBL Assay Science代理

网站首页产品中心代理品牌新闻资讯资源中心关于榴莲视频成版APP下载

所在位置：首页 > 产品中心 > Antibodies > Antibodies产品

订购信息

上海榴莲视频成版APP下载生物科技公司

Tel:400-968-7988 021-33779008

Anti-CFI Antibody

品牌：Antibodies

货号：

规格：50µl

货期：

应用：

咨询客服

立即购买加入购物车

Anti-CFI Antibody

商品详情参考文献相关资料

Overview

Name:	Anti-CFI Antibody See all CFI primary antibodies
Description:	Rabbit polyclonal antibody to CFI.
Applications:	WB, IHC, IF
Dilutions:	WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:100.
Reactivity:	Human
Immunogen:	Recombinant protein of human CFI.
Protein Length:	583
Host:	Rabbit
Clonality:	Polyclonal
Isotype:	IgG
Conjugate:	Unconjugated
Purification:	Affinity purification.
Product Form:	Liquid
Formulation:	Supplied in Phosphate Buffered Saline, pH 7.30, with 0.02% Sodium Azide and 50% Glycerol.
Storage:	Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

Target

Function:	Responsible for cleaving the alpha-chains of C4b and C3b in the presence of the cofactors C4-binding protein and factor H respectively.
Tissue Specificity:	Plasma.
Involvement in Disease:	Hemolytic uremic syndrome atypical 3: An atypical form of hemolytic uremic syndrome. It is a complex genetic disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, renal failure and absence of episodes of enterocolitis and diarrhea. In contrast to typical hemolytic uremic syndrome, atypical forms have a poorer prognosis, with higher death rates and frequent progression to end-stage renal disease. Complement factor I deficiency: Autosomal recessive condition associated with a propensity to pyogenic infections. Macular degeneration, age-related, 13: A form of age-related macular degeneration, a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.
Sequence Similarities:	Belongs to the peptidase S1 family.
Cellular locations:	Secreted > Extracellular space.
Database Links:	Entrez Gene: 3426?Human Omim: 217030?Human SwissProt: P05156?Human Unigene: 312485?Human
Synonyms:	AHUS3 Antibody ARMD13 Antibody C3b INA Antibody C3b inactivator Antibody C3B/C4B inactivator Antibody C3BINA Antibody CFAI_HUMAN Antibody Cfi Antibody Complement component I Antibody Complement control protein factor I Antibody Complement factor I Antibody Complement factor I heavy chain Antibody Complement factor I light chain Antibody F1 Antibody Factor I Antibody FactorI Antibody FI Antibody I factor Antibody IF Antibody KAF Antibody Konglutinogen activating factor Antibody Light chain of factor I Antibody OTTHUMP00000219728 Antibody OTTHUMP00000221928 Antibody
Information:	Target information shown above is from the UniProt Consortium.