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華瑞科研網(wǎng)-ELISA試劑盒
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華瑞科研網(wǎng)-ELISA試劑盒
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所 在 地上海市
聯(lián)系方式：韓經(jīng)理查看聯(lián)系方式
更新時(shí)間：2018-04-07 13:27:42瀏覽次數(shù)：318次
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經(jīng)營(yíng)模式：生產(chǎn)廠家
商鋪產(chǎn)品：9992條
所在地區(qū)：上海上海市
聯(lián)系人：韓經(jīng)理 （銷(xiāo)售）
“Anti-RSL1D1抗體,細(xì)胞衰老抑制基因抗體科研"我公司擁有*的細(xì)胞服務(wù)技術(shù)，*的儀器設(shè)備和專(zhuān)業(yè)的ELISA檢測(cè)試劑盒、生物索標(biāo)記、熒光索標(biāo)記、酶標(biāo)記等，廣泛用于多種分析研究與技術(shù)測(cè)定。咨詢(xún)，我們將竭誠(chéng)為你服務(wù)！
Anti-RSL1D1抗體,細(xì)胞衰老抑制基因抗體科研產(chǎn)品介紹：
RSL1D1, also known as CATX-11, PBK1, L12 or CSIG, is a 490 amino acid nuclear protein that belongs to the ribosomal protein L1P family. Expressed in placenta, RSL1D1 contains many phosphorylated amino acid residues and is encoded by a gene that maps to human chromosome 16p13.13. Chromosome 16 encodes over 900 genes in approximay 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias.
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產(chǎn)品詳情：
產(chǎn)品編號(hào)：HRK-0793R
產(chǎn)品規(guī)格: 0.1ml/0.2ml
產(chǎn)品別名：CATX 11; CATX-11; CATX11; Cellular senescence inhibited gene protein; L12; PBK1; CSIG; L12; PBK1; Protein PBK1; Ribosomal L1 domain-containing protein 1; RL1D1_HUMAN; RSL1D1; Ribosomal L1 domain containing 1
產(chǎn)品價(jià)格：詢(xún)價(jià)(電詢(xún)或客服)
產(chǎn)品用途：科研實(shí)驗(yàn)
貯 存： 貯存于-20℃.
與“"有關(guān)的其他產(chǎn)品：
Anti-factor ⅩⅢ（coagulation factor ⅩⅢ） *13抗體
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Anti-FAK（Focal adhesin kinase） 粘著斑激酶抗體
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Anti-FAF1(Fas associated factor 1) Fas相關(guān)1因子抗體
Anti-phospho-FAK(pSer732)(phospho-Focal adhesion kinase) 抗磷酸化粘著斑激酶抗體
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