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  • IHC0110蛋白單克隆即用型免疫組化試劑盒

    S100 beta is a member of the S100 family of proteins containing 2 EF-hand calcium binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such a

    更新時間:2025-03-10
    型號:IHC0110
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:342
  • IHC0107R大鼠髓鞘堿性蛋白/磷脂堿性蛋白即用型免疫組化試劑盒

    Oligodendrocyte Marker $nThe classic group of Myelin basic protein (MBP) isoforms (isoforms 4 to 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller

    更新時間:2025-03-10
    型號:IHC0107R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:315
  • IHC0107M小鼠髓鞘堿性蛋白/磷脂堿性蛋白即用型免疫組化試劑盒

    Oligodendrocyte Marker $nThe classic group of Myelin basic protein (MBP) isoforms (isoforms 4 to 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller

    更新時間:2025-03-10
    型號:IHC0107M
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:332
  • IHC0107H人髓鞘堿性蛋白/磷脂堿性蛋白即用型免疫組化試劑盒

    Oligodendrocyte Marker $nThe classic group of Myelin basic protein (MBP) isoforms (isoforms 4 to 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller

    更新時間:2025-03-10
    型號:IHC0107H
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:342
  • IHC0107髓鞘堿性蛋白/磷脂堿性蛋白即用型免疫組化試劑盒

    Oligodendrocyte Marker $nThe classic group of Myelin basic protein (MBP) isoforms (isoforms 4 to 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller

    更新時間:2025-03-10
    型號:IHC0107
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:337
  • IHC0101R大鼠膠質(zhì)纖維酸性蛋白即用型免疫組化試劑盒

    This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocyt

    更新時間:2025-03-10
    型號:IHC0101R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:359
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