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黑色素瘤抗原樣基因2抗體

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產(chǎn)品名稱: 黑色素瘤抗原樣基因2抗體
產(chǎn)品型號: MAGEL2
產(chǎn)品展商: 單克隆抗體/多克隆抗體
產(chǎn)品文檔: 無相關(guān)文檔

簡單介紹

黑色素瘤抗原樣基因2抗體應(yīng)用于IHC、WB、 IF、IP、ELISA等科研實(shí)驗(yàn),按理化性質(zhì)和生物學(xué)功能IgM、IgG、IgA、IgE、IgD五類。按抗體的來源,可將其分為天然抗體和**抗體。黑色素瘤抗原樣基因2抗體生產(chǎn)每個流程都執(zhí)行嚴(yán)格的檢測標(biāo)準(zhǔn),保證蛋白抗原產(chǎn)品質(zhì)量,質(zhì)量穩(wěn)定,實(shí)驗(yàn)效果明顯。


黑色素瘤抗原樣基因2抗體  的詳細(xì)介紹

黑色素瘤抗原樣基因2抗體

規(guī)格:1mg/1ml

英文名: MAGEL2

別名: Mage-l2; MAGE-like 2; MAGE-like protein 2; MAGEL2; melanoma antigen-like gene 2; NDNL1; necdin-like 1; nM15; ns7.

分子量: 59kDa

儲存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆類型:Polyclonal

亞型:IgG

純化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human MAGEL2

交叉反應(yīng):Human, Mouse, Rat, Dog, Pig, Cow,

細(xì)胞定位:

黑色素瘤抗原樣基因2抗體產(chǎn)品介紹:background: Melanoma-associated antigen (MAGE) are completely silent in normal tissues, with the exception of male germ cells, and, for some of them, placenta. These antigens ought to be strictly tumor specific, expressed in tumor cells of various histological types. Because of their specific expression on tumor cells, these antigens are of particular interest for antitumor immunotherapy. Genes of the MAGE family direct the expression of tumor antigens that are recognized on a human melanoma by autologous cytolytic T lymphocytes. Though the function of MAGE is unknown, may play a role in embryonal development and tumor transformation or aspects of tumor progression. Function: May enhance ubiquitin ligase activity of RING-type zinc finger-containing E3 ubiquitin-protein ligases. Proposed to act through recruitment and/or stabilization of the Ubl-conjugating enzyme (E2) at the E3:substrate complex. Subunit: Interacts with TRIM27. 黑色素瘤抗原樣基因2抗體Tissue Specificity: Expressed in placenta, fetal and ***** brain. Not detected in heart and small intestine, very low levels in fibroblasts. Not expressed in brain of a Prader-Willi patient. DISEASE: Note=May play a role in Prader-Willi syndrome (PWS) which is a contiguous gene syndrome resulting from inactivity of the paternal copies of a number of genes on 15q11, through deletion or disruption of these genes or maternal uniparental disomy 15. The PWS syndrome is characterized by muscular hypotonia, mental retardation, short stature, obesity, 黑色素瘤抗原樣基因2抗體hypogonadotropic hypogonadism, and small hands and feet. Similarity: Contains 1 MAGE domain. Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

黑色素瘤抗原樣基因2抗體產(chǎn)品應(yīng)用:ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù)) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究領(lǐng)域:腫瘤  **學(xué)  細(xì)胞類型標(biāo)志物  腫瘤細(xì)胞生物標(biāo)志物  

儲存條件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

來源: Rabbit

外觀: Lyophilized or Liquid




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