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PERM (84k, Cleaved-Ser155) Rabbit Polyclonal Antibody
A-DK16739
PERM (84k, Cleaved-Ser155) Rabbit Polyclonal Antibody
货号 纯度 规格 目录价 会员价 库存 数量 购买
A-DK16739-50μg 50μg 50μg ¥1100.00 登录查看
A-DK16739-100μg 100μg 100μg ¥2000.00 登录查看
产品详情

产品名称

PERM (84k, Cleaved-Ser155) Rabbit Polyclonal Antibody

英文名称

PERM (84k, Cleaved-Ser155) Rabbit Polyclonal Antibody

类别

抗体产品

反应种属

Human,Rat,Mouse

应用

WB,ELISA,IHC-P

别名

Myeloperoxidase (MPO;EC 1.11.2.2) [Cleaved into: Myeloperoxidase; 89 kDa myeloperoxidase; 84 kDa myeloperoxidase; Myelopero

xidase light chain; Myeloperoxidase heavy chain]

宿主

Rabbit

Clonality

Polyclonal

Human Gene ID

 4353

Mouse Gene ID

17523

浓度

1 mg/ml

基因名称

MPO

蛋白名称

PERM (84k, Cleaved-Ser155)

存储缓冲液

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

免疫原

Synthesized peptide derived from human PERM (84k, Cleaved-Ser155)

稀释度

WB 1:500-2000, IHC-P 1:50-300, ELISA 2000-20000

预测分子量

65 84kDa

运输及保存条件

-20°C/1 year

同种型

Rabbit,IgG

细胞定位

Lysosome.

背景介绍

Myeloperoxidase (MPO) is a heme protein synthesized during myeloid differentiation that constitutes the major component of
neutrophil azurophilic granules. Produced as a single chain precursor, myeloperoxidase is subsequently cleaved into a light
and heavy chain. The mature myeloperoxidase is a tetramer composed of 2 light chains and 2 heavy chains. This enzyme produ
ces hypohalous acids central to the microbicidal activity of neutrophils. [provided by RefSeq, Nov 2014],

纯化

The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

特异性

This antibody detects endogenous levels of Human PERM (84k, Cleaved-Ser155, protein was cleaved amino acid sequence between

154-155)

功能

catalytic activity:Cl(-) + H(2)O(2) = HOCl + 2 H(2)O.,catalytic activity:Donor + H(2)O(2) = oxidized donor + 2 H(2)O.,cofac
tor:Binds 1 calcium ion per heterodimer.,cofactor:Binds 1 heme B (iron-protoporphyrin IX) group covalently per heterodimer.
,disease:Defects in MPO are the cause of myeloperoxidase deficiency (MPD) [MIM:254600]. MPD is an autosomal recessive defec
t that results in disseminated candidiasis.,function:Part of the host defense system of polymorphonuclear leukocytes. It is
responsible for microbicidal activity against a wide range of organisms. In the stimulated PMN, MPO catalyzes the producti
on of hypohalous acids, primarily hypochlorous acid in physiologic situations, and other toxic intermediates that greatly e
nhance PMN microbicidal activity.,online information:MPO mutation db,online information:Myeloperoxidase entry,similarity:Be
longs to the peroxidase family. XPO subfamily.,subunit:Tetramer of two light chains and two heavy chains.,

                           

Immunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).

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