亚洲天堂av 在线,亚洲精品无码久久久久av麻豆

您好，歡迎來到拜力生物網(wǎng)站！請登錄注冊

我的訂單 | 聯(lián)系我們 | 在線客服QQ：3012681483 | 客服電話：400-968-7988 | 工作時間：08:30-17:30

主營產(chǎn)品： ELISA試劑盒、抗體、補體血清、兔補體、干擾素、小鼠測溫儀、進口試劑、Quidel代理、Swant代理、PBL Assay Science代理

網(wǎng)站首頁產(chǎn)品中心代理品牌新聞資訊資源中心關(guān)于我們

所在位置：首頁 > 產(chǎn)品中心 > Antibodies > Antibodies產(chǎn)品

訂購信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Anti-CTSA Antibody

品牌：Antibodies

貨號：

規(guī)格：50μl

貨期：

應(yīng)用：

咨詢客服

立即購買加入購物車

Anti-CTSA Antibody

商品詳情參考文獻相關(guān)資料

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.