Anti-CYP17A1 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-CYP17A1 Antibody

品牌：Antibodies

货号：

规格：100µg

货期：

应用：

咨询客服

立即购买加入购物车

Anti-CYP17A1 Antibody

商品详情参考文献相关资料

Overview

Name:	Anti-CYP17A1 Antibody See all CYP17A1 primary antibodies
Description:	Goat polyclonal antibody to CYP17A1.
Applications:	ELISA, WB, IHC
Reactivity:	Human
Immunogen:	Synthetic peptide corresponding to Human CYP17A1 (internal region).
Sequence:	C-LFKDGDQKLEK
Host:	Goat
Clonality:	Polyclonal
Isotype:	IgG
Conjugate:	Unconjugated
Purification:	Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Concentration:	100 μg at 0.5 mg/ml.
Product Form:	Liquid
Formulation:	Supplied in Tris Buffered Saline, pH 7.30, with 0.02% Sodium Azide and 0.5% BSA.
Storage:	Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

Target

Function:	Conversion of pregnenolone and progesterone to their 17-alpha-hydroxylated products and subsequently to dehydroepiandrosterone (DHEA) and androstenedione. Catalyzes both the 17-alpha-hydroxylation and the 17,20-lyase reaction. Involved in sexual development during fetal life and at puberty.
Involvement in Disease:	Adrenal hyperplasia 5: A form of congenital adrenal hyperplasia, a common recessive disease due to defective synthesis of cortisol. Congenital adrenal hyperplasia is characterized by androgen excess leading to ambiguous genitalia in affected females, rapid somatic growth during childhood in both sexes with premature closure of the epiphyses and short ***** stature. Four clinical types: 'salt wasting' (SW, the most severe type), 'simple virilizing' (SV, less severely affected patients), with normal aldosterone biosynthesis, 'non-classic form' or late-onset (NC or LOAH) and 'cryptic' (asymptomatic).
Sequence Similarities:	Belongs to the cytochrome P450 family.
Post-Translational Modification:	Phosphorylation is necessary for 17,20-lyase, but not for 17-alpha-hydroxylase activity.
Cellular Location:	Membrane.
Database Links:	Entrez Gene: 1586?Human Omim: 609300?Human SwissProt: P05093?Human Unigene: 438016?Human
Synonyms:	20 lyase Antibody CP17A_HUMAN Antibody CPT7 Antibody CYP17 Antibody CYP17A1 Antibody CYPXVII Antibody Cytochrome P450 17A1 Antibody Cytochrome P450 family 17 Antibody Cytochrome P450 family 17 subfamily A polypeptide 1 Antibody Cytochrome p450 subfamily XVII (steroid 17 alpha hydroxylase) adrenal hyperplasia Antibody Cytochrome p450 XVIIA1 Antibody Cytochrome P450-C17 Antibody Cytochrome P450c17 Antibody OTTHUMP00000020382 Antibody P450 C17 Antibody P450c17 Antibody S17AH Antibody Steroid 17 alpha hydroxylase/17,20 lyase Antibody Steroid 17 alpha monooxygenase Antibody Steroid 17-alpha-hydroxylase/17 Antibody Steroid 17-alpha-monooxygenase Antibody
Information:	Target information shown above is from the UniProt Consortium.