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黑色素瘤相關(guān)抗原C1抗體

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產(chǎn)品名稱: 黑色素瘤相關(guān)抗原C1抗體
產(chǎn)品型號(hào): MAGEC1
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(jiǎn)單介紹

黑色素瘤相關(guān)抗原C1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。黑色素瘤相關(guān)抗原C1抗體生產(chǎn)每個(gè)流程都執(zhí)行嚴(yán)格的檢測(cè)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。


黑色素瘤相關(guān)抗原C1抗體  的詳細(xì)介紹

黑色素瘤相關(guān)抗原C1抗體

規(guī)格:1mg/1ml

英文名: MAGEC1

別名: Cancer/testis antigen 7.1; Cancer/testis antigen family 7 member 1; CT7; CT7.1; MAGC1_HUMAN; MAGE C1; MAGE C1 antigen; MAGE-C1 antigen; MAGEC1; melanoma antigen family C, 1; Melanoma associated antige

分子量: 124kDa

儲(chǔ)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 MAGEC1

交叉反應(yīng):Human,

細(xì)胞定位:

黑色素瘤相關(guān)抗原C1抗體產(chǎn)品介紹:background: This gene is a member of the melanoma antigen gene (MAGE) family. The proteins of this family are tumor-specific antigens that can be recognized by autologous cytolytic T lymphocytes. This protein contains a large number of unique short repetitive sequences in front of the MAGE-homologous sequence, and therefore is about 800 aa longer than the other MAGE proteins. [provided by RefSeq, Jul 2008] 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. Subcellular Location: 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. Tissue Specificity: Expressed in testis and in tumors of a wide variety of histologic types.黑色素瘤相關(guān)抗原C1抗體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, hypogonadotropic hypogonadism,黑色素瘤相關(guān)抗原C1抗體 and small hands and feet. Similarity: Contains 1 MAGE domain. Gene ID: 9947 Database links: Entrez Gene: 9947 Human Omim: 300223 Human SwissProt: O60732 Human Unigene: 132194 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

黑色素瘤相關(guān)抗原C1抗體產(chǎn)品應(yīng)用:WB=1:100-500 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  細(xì)胞類型標(biāo)志物  腫瘤細(xì)胞生物標(biāo)志物  

儲(chǔ)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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