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  • bsm-63199R補(bǔ)體C3重組兔單抗

    The complement factor C3 consists of an alpha and a beta chain. C3 is a central factor in the complement cascade. It is central to the alternative pathway that leads to the C3 convertase C3bBb. The classical mannose binding lectin activation pathway leads to the C3 convertase C4b2a. These convertases cleave C3 resulting in C3a and C3b. Further degradation leads to the formation of the alpha chain products C3d, C3g and C3c. C3 is an acute phase protein that is produced by a wide range of tiss

    更新時間:2025-03-05
    型號:bsm-63199R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:402
  • bsm-63198R轉(zhuǎn)甲狀腺素蛋白重組兔單抗

    This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral ne

    更新時間:2025-03-05
    型號:bsm-63198R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:391
  • bsm-63196RCD19重組兔單抗

    This gene encodes a member of the immunoglobulin gene superfamily. Expression of this cell surface protein is restricted to B cell lymphocytes. This protein is a reliable marker for pre-B cells but its expression diminishes during terminal B cell differentiation in antibody secreting plasma cells. The protein has two N-terminal extracellular Ig-like domains separated by a non-Ig-like domain, a hydrophobic transmembrane domain, and a large C-terminal cytoplasmic domain. This protein forms a com

    更新時間:2025-03-05
    型號:bsm-63196R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:411
  • bsm-63195R微小細(xì)胞血癥相關(guān)轉(zhuǎn)錄因子重組兔單抗

    The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. [provided by RefSeq, Aug 2017]

    更新時間:2025-03-05
    型號:bsm-63195R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:383
  • bsm-63194RCD19重組兔單抗

    This gene encodes a member of the immunoglobulin gene superfamily. Expression of this cell surface protein is restricted to B cell lymphocytes. This protein is a reliable marker for pre-B cells but its expression diminishes during terminal B cell differentiation in antibody secreting plasma cells. The protein has two N-terminal extracellular Ig-like domains separated by a non-Ig-like domain, a hydrophobic transmembrane domain, and a large C-terminal cytoplasmic domain. This protein forms a com

    更新時間:2025-03-05
    型號:bsm-63194R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:428
  • bsm-63192RS100A9重組兔單抗

    The protein encoded by this gene 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 as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in the inhibition of casein kinase and altered expressio

    更新時間:2025-03-05
    型號:bsm-63192R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:395
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