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  • bsm-62930R細(xì)胞骨架蛋白C端PDLIM1重組兔單抗

    PDLIM1 is a cytoskeletal protein that may act as an adapter that brings other proteins to the cytoskeleton. PDLIM1 is strongly expressed in the heart $nand skeletal muscle, moderately expressed in the spleen, small intestine, colon, placenta, and lung, and minimally expressed in liver, thymus, kidney, prostate and pancreas. $nIt is not found in the brain, testis, ovary, and peripheral blood leukocytes.

    更新時(shí)間:2025-03-04
    型號(hào):bsm-62930R
    廠(chǎng)商性質(zhì):生產(chǎn)廠(chǎng)家
    瀏覽量:111
  • bsm-62928R肝癌衍生生長(zhǎng)因子/高遷移率族蛋白1樣蛋白2重組兔單抗

    This gene encodes a member of the hepatoma-derived growth factor family. The encoded protein has mitogenic and DNA-binding activity and may play a role in cellular proliferation and differentiation. This gene was thought initially to be located on chromosome X, however, that location has been determined to correspond to a related pseudogene. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]

    更新時(shí)間:2025-03-04
    型號(hào):bsm-62928R
    廠(chǎng)商性質(zhì):生產(chǎn)廠(chǎng)家
    瀏覽量:82
  • bsm-62926R轉(zhuǎn)錄因子OTX1重組兔單抗

    Transcription factors, OTX1 and OTX2, are two murine homologs of the Drosophila orthodenticle (OTD), show a limited amino acid sequence divergence. OTX1 and OTX2 play an important role during early and later events required for proper brain development in that they are involved in the processes of induction, specification and regionalization of the brain. OTX1 is involved in corticogenesis, sensory organ development and pituitary functions, while OTX2 is necessary earlier in development, f

    更新時(shí)間:2025-03-04
    型號(hào):bsm-62926R
    廠(chǎng)商性質(zhì):生產(chǎn)廠(chǎng)家
    瀏覽量:84
  • bsm-62924R類(lèi)固醇脫氫酶樣蛋白NSDHL重組兔單抗

    NSDHL is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.

    更新時(shí)間:2025-03-04
    型號(hào):bsm-62924R
    廠(chǎng)商性質(zhì):生產(chǎn)廠(chǎng)家
    瀏覽量:79
  • bsm-62923R類(lèi)固醇脫氫酶樣蛋白NSDHL重組兔單抗

    NSDHL is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.

    更新時(shí)間:2025-03-04
    型號(hào):bsm-62923R
    廠(chǎng)商性質(zhì):生產(chǎn)廠(chǎng)家
    瀏覽量:92
  • bsm-62922R原癌基因N-Ras重組兔單抗

    N-RAS (neuroblastoma RAS viral oncogene homolog) analogously to other GTP-binding proteins (such as Translation Elongation Factor EFTu or signal transducing G-Proteins) RAS proteins are involved in signal transduction pathways, ras gene family is part of the ras superfamily including the mammalian RAS, RAL, RAC, RHO, RAP, and RAB gene families and the yeast homologs like SEC4 and YPT1 genes; genes encode small monomeric proteins of low molecular mass (20-30 kDa) which share at least 30% homo

    更新時(shí)間:2025-03-04
    型號(hào):bsm-62922R
    廠(chǎng)商性質(zhì):生產(chǎn)廠(chǎng)家
    瀏覽量:84
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