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無胸腺癥關(guān)鍵蛋白6樣抗體(迪格奧爾格綜合征)說明書

時(shí)間:2022-4-7閱讀:37
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英文名稱    DGCR6L   

中文名稱    無胸腺癥關(guān)鍵蛋白6樣抗體(迪格奧爾格綜合征)   

別    名    DGC6L_HUMAN; DGCR6L; DiGeorge syndrome critical region 6-like protein; Protein DGCR6L.   

供應(yīng)商    遠(yuǎn)慕生物

研究領(lǐng)域    腫瘤  細(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)     

抗體來源    Rabbit   

克隆類型    Polyclonal   

交叉反應(yīng)    Human, Mouse, Rat, Cow, Rabbit,    

產(chǎn)品應(yīng)用    WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 無胸腺癥關(guān)鍵蛋白6樣抗體(迪格奧爾格綜合征)(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.   

分 子 量    25kDa   

細(xì)胞定位    細(xì)胞核    

性    狀    Lyophilized or Liquid   

濃    度    1mg/1ml   

免 疫 原    KLH conjugated synthetic peptide derived from human DGCR6L   

亞    型    IgG   

純化方法    affinity purified by Protein A   

儲(chǔ) 存 液    Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4   

保存條件    Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.   

 

無胸腺癥關(guān)鍵蛋白6樣抗體(迪格奧爾格綜合征)產(chǎn)品介紹    background:

Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin-1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterized by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt’s lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.

 

Function:
May play a role in neural crest cell migration into the third and fourth pharyngeal pouches.

Subcellular Location:
Nucleus. Predominantly nuclear.

 

Tissue Specificity:
Widely expressed in fetal and adult tissues. Highest expression in liver, heart and skeletal muscle. Lower levels in pancreas and placenta. Weak expression in brain.

 

Similarity:
Belongs to the gonadal family.    

 

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