欢迎来到启研生物[ 会员登录 ] [ 立即注册 ]
400-812-0026

购物车0

您购物车为空,赶紧选购吧!
CPN Polyclonal Antibody
CPN Polyclonal Antibody
CPN Polyclonal Antibody
市场价格
经销商客户: ¥214.5
实验室客户: ¥292.5
近期销售量17 用户评价:comment rank 5()
文件与质量管理
浏览历史 [清空]

商品描述

商品属性

Target:CPN cat

Gene Name:CPN1

Protein Name:Carboxypeptidase N catalytic chain

Human Gene Id:1369

Human Swiss Prot No:P15169

Mouse Swiss Prot No:Q9JJN5

Immunogen:The antiserum was produced against synthesized peptide derived from human CPN1. AA range:409-458

Specificity:CPN cat Polyclonal Antibody detects endogenous levels of CPN cat protein.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500 - 1:2000. ELISA: 1:20000. Not yet tested in other applications.

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name:CPN1;ACBP;Carboxypeptidase N catalytic chain;CPN;Anaphylatoxin inactivator;Arginine carboxypeptidase;Carboxypeptidase N polypeptide 1;Carboxypeptidase N small subunit;Kininase-1;Lysine carboxypeptidase;Plasma carboxypeptidase B;S

Observed Band(KD):total 52kD,Cleaved 48kD

Background: Carboxypeptidase N is a plasma metallo-protease that cleaves basic amino acids from the C terminal of peptides and proteins. The enzyme is important in the regulation of peptides like kinins and anaphylatoxins, and has also been known as kininase-1 and anaphylatoxin inactivator. This enzyme is a tetramer comprised of two identical regulatory subunits and two identical catalytic subunits; this gene encodes the catalytic subunit. Mutations in this gene can be associated with angioedema or chronic urticaria resulting from carboxypeptidase N deficiency. [provided by RefSeq, Jul 2008],

Function:catalytic activity:Release of a C-terminal basic amino acid, preferentially lysine.,cofactor:Binds 1 zinc ion per subunit.,disease:Defects in CPN1 are the cause of carboxypeptidase N deficiency [MIM:212070]. Patients affected present some combination of angioedema or chronic urticaria, as well as hay fever or astma, and have also slightly depressed serum carboxy peptidase N, suggestive of autosomal recessive inheritance of this disorder.,function:Protects the body from potent vasoactive and inflammatory peptides containing C-terminal Arg or Lys (such as kinins or anaphylatoxins) which are released into the circulation.,similarity:Belongs to the peptidase M14 family.,subunit:Tetramer of two catalytic chains and two glycosylated inactive chains.,tissue specificity:Synthesized in the liver and secreted in plasma.,

Subcellular Location:Secreted, extracellular space.

Expression:Synthesized in the liver and secreted in plasma.

广告说明