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  • bsm-62516R蛋白磷酸酶6調節(jié)亞基C重組兔單抗

    This gene encodes the catalytic subunit of protein phosphatase, a component of a signaling pathway regulating cell cycle progression. Splice variants encoding different protein isoforms exist. The pseudogene of this gene is located on chromosome X. [provided by RefSeq, Jul 2008]

    更新時間:2025-03-04
    型號:bsm-62516R
    廠商性質:生產廠家
    瀏覽量:133
  • bsm-62515R抑癌基因NDRG3重組兔單抗

    The NDRG3 protein is a 41 kDa cytoplasmic protein that exists in three isoforms, the first of which is the canonical 41 kDa, 375 amino acid form. It is a member of the NDRG family of proteins and is involved in cell differentiation and negative regulation of cell growth.

    更新時間:2025-03-04
    型號:bsm-62515R
    廠商性質:生產廠家
    瀏覽量:115
  • bsm-62514R黑素皮質素受體5重組兔單抗

    The melanocortin family comprises the Alpha-, Beta- and Gamma- melanocyte stimulating hormones (MSH) and adrenocorticotrophin. The receptors for these hormones are seven-transmembrane G protein-coupled proteins that activate adenylyl cyclase. Five melanocortin receptors have been cloned and shown to exhibit different affinities and patterns of expression. MC1-R (MSH-R) is expressed in melanocytes and corticoadrenal tissue. MC2-R is the ACTH receptor and is expressed primarily in the adren

    更新時間:2025-03-04
    型號:bsm-62514R
    廠商性質:生產廠家
    瀏覽量:111
  • bsm-62513RCAP1重組兔單抗

    更新時間:2025-03-03
    型號:bsm-62513R
    廠商性質:生產廠家
    瀏覽量:122
  • bsm-62512R細胞毒性受體NK-p44重組兔單抗

    NCR2 (NKp44) is a member of the natural cytotoxicity receptor (NCR) family that is expressed on activated human NK cells. NCR2 displays a single extracellular Ig-like V domain and a transmembrane portion containing the charged residue (Lysine), likely involved in the association with KARAP/DAP12 molecules. Gene coding for NCR2 maps on human chromosome 6p21.1

    更新時間:2025-03-03
    型號:bsm-62512R
    廠商性質:生產廠家
    瀏覽量:111
  • bsm-62511RELP4蛋白重組兔單抗

    This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul

    更新時間:2025-03-03
    型號:bsm-62511R
    廠商性質:生產廠家
    瀏覽量:130
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