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MPO Mouse mAb (bsm-43010M)  
訂購熱線:400-901-9800
訂購郵箱:[email protected]
訂購QQ:  400-901-9800
技術(shù)支持:[email protected]
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)

產(chǎn)品編號 bsm-43010M
英文名稱 MPO Mouse mAb
中文名稱 髓過氧化物酶單克隆抗體
別    名 Myeloperoxidase; c-ANCA; 89 kDa myeloperoxidase; 84 kDa yeloperoxidase; Myeloperoxidase light chain; Myeloperoxidase heavy chain; EC 1.11.1.7; PERM_HUMAN.  
抗體來源 Mouse
克隆類型 Monoclonal
交叉反應(yīng) Human
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 84 kDa
檢測分子量
細(xì)胞定位 細(xì)胞漿 
性    狀 Liquid
免 疫 原 Recombinant human MPO protein 
亞    型
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 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 produces hypohalous acids central to the microbicidal activity of neutrophils. [provided by RefSeq, Nov 2014]

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 production of hypohalous acids, primarily hypochlorous acid in physiologic situations, and other toxic intermediates that greatly enhance PMN microbicidal activity.

Subunit:
Tetramer of two light chains and two heavy chains.

Subcellular Location:
Lysosome.

DISEASE:
Defects in MPO are the cause of myeloperoxidase deficiency (MPD) [MIM:254600]. MPD is an autosomal recessive defect that results in disseminated candidiasis.

Similarity:
Belongs to the peroxidase family. XPO subfamily.

SWISS:
P05164

Gene ID:
4353

Database links:

Entrez Gene: 4353 Human

Entrez Gene: 17523 Mouse

Entrez Gene: 303413 Rat

Omim: 606989 Human

SwissProt: P05164 Human

SwissProt: P11247 Mouse

Unigene: 458272 Human

Unigene: 4668 Mouse

Unigene: 47782 Rat



髓過氧化物酶MPO,作為一種白細(xì)胞酶,具有介導(dǎo)炎性反應(yīng)、調(diào)節(jié)免疫應(yīng)答等多種功能,并可參與疾病的發(fā)生發(fā)展過程。同時(shí),髓過氧化物酶基因存在基因多態(tài)性,也影響機(jī)體對疾病的易感性. 在正常淋巴組織中和各種髓樣細(xì)胞增生癥中,MPO均有較強(qiáng)表達(dá),如:淋巴樣細(xì)胞、原核細(xì)胞、肥大細(xì)胞、漿細(xì)胞以及各種上皮源性腫瘤和肉瘤等。
髓過氧化物酶(myeloperoxidase,MPO),是一種血紅素蛋白,富含于中性粒細(xì)胞中,由粒細(xì)胞進(jìn)入循環(huán)之前在骨髓內(nèi)合成并存儲于噬天青顆粒內(nèi)。外界刺激可導(dǎo)致中性粒細(xì)胞聚集,從而釋放髓過氧化物酶。MPO的相對分子量為150kDa,是由兩個(gè)亞單位通過共價(jià)結(jié)合形成的四聚體,每個(gè)亞單位又有一條重鏈α(相對分子量60kDa)和一條輕鏈β鏈(相對分子量為15kDa)構(gòu)成。(重鏈和輕鏈通過二硫鍵結(jié)合)
產(chǎn)品圖片
Paraformaldehyde-fixed, paraffin embedded Human Gastric cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with MPO Monoclonal Antibody, Unconjugated(bsm-43010M) at 1:200 overnight at 4°C, followed by con
Paraformaldehyde-fixed, paraffin embedded Human tonsils; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with MPO Monoclonal Antibody, Unconjugated(bsm-43010M) at 1:200 overnight at 4°C, followed by conjugatio
Paraformaldehyde-fixed, paraffin embedded Human colon cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with MPO Monoclonal Antibody, Unconjugated(bsm-43010M) at 1:200 overnight at 4°C, followed by conju
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