Anti-CTSA Antibody |产品详情|进口试剂采购网

您好，欢迎来到拜力生物网站！请登录注册

我的订单 | 联系我们 | 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试剂盒、抗体、补体血清、兔补体、干扰素、小鼠测温仪、进口试剂、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我们

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

订购信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Anti-CTSA 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-CTSA Antibody

商品详情参考文献相关资料

Overview

Name:	Anti-CTSA Antibody See all CTSA primary antibodies
Description:	Rabbit polyclonal antibody to CTSA.
Applications:	WB, IF
Dilutions:	WB: 1:500 - 1:2000, IF: 1:20 - 1:50.
Reactivity:	Human, Mouse, Rat
Immunogen:	Recombinant protein of human CTSA.
Protein Length:	480
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:	Protective protein appears to be essential for both the activity of beta-galactosidase and neuraminidase, it associates with these enzymes and exerts a protective function necessary for their stability and activity. This protein is also a carboxypeptidase and can deamidate tachykinins.
Involvement in Disease:	Galactosialidosis: A lysosomal storage disease associated with a combined deficiency of beta-galactosidase and neuraminidase, secondary to a defect in cathepsin A. All patients have clinical manifestations typical of a lysosomal disorder, such as coarse facies, cherry red spots, vertebral changes, foam cells in the bone marrow, and vacuolated lymphocytes. Three phenotypic subtypes are recognized. The early infantile form is associated with fetal hydrops, edema, ascites, visceromegaly, skeletal dysplasia, and early death. The late infantile type is characterized by hepatosplenomegaly, growth retardation, cardiac involvement, and a normal or mildly affected mental state. The juvenile/***** form is characterized by myoclonus, ataxia, angiokeratoma, mental retardation, neurologic deterioration, absence of visceromegaly, and long survival.
Sequence Similarities:	Belongs to the peptidase S10 family.
Cellular Location:	Lysosome.
Database Links:	Entrez Gene: 5476 Human Entrez Gene: 19025 Mouse Entrez Gene: 296370 Rat Omim: 613111 Human SwissProt: P10619 Human SwissProt: P16675 Mouse Unigene: 609336 Human Unigene: 359633 Mouse Unigene: 474586 Mouse Unigene: 104631 Rat
Synonyms:	beta galactosidase 2 Antibody BETA GALACTOSIDASE PROTECTIVE PROTEIN Antibody beta-galactosidase 2 Antibody beta-galactosidase protective protein Antibody betagalactosidase 2 Antibody Carboxypeptidase C Antibody Carboxypeptidase L Antibody carboxypeptidase Y-like kininase Antibody Cathepsin A Antibody Ctsa Antibody deamidase Antibody EC 3.4.16.5 Antibody Glactosialidosis Antibody GLB2 Antibody Goldberg Syndrome Antibody GSL Antibody lysosomal carboxypeptidase A Antibody Lysosomal protective protein Antibody Lysosomal protective protein 20 kDa chain Antibody Lysosomal protective protein deficiency Antibody NEURAMINIDASE BETA GALACTOSIDASE EXPRESSION; NGBE Antibody Neuraminidase deficiency with beta-galactosidase deficiency Antibody NGBE Antibody OTTHUMP00000031778 Antibody OTTHUMP00000031781 Antibody PPCA Antibody PPCA deficiency Antibody PPGB Antibody PPGB_HUMAN Antibody Protective protein cathepsin A Antibody Protective protein for beta galactosidase Antibody Protective protein for beta-galactosidase Antibody Protective protein/Cathepsin A (PPCA) Antibody Protective protein/cathepsin A deficiency Antibody urinary kininase Antibody
Information:	Target information shown above is from the UniProt Consortium.