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  • bsm-61100R環(huán)指蛋白20重組兔單抗

    RNF20 is an E3 ubiquitin ligase protein that mediates monoubiquitination of histone H2B and the methylation of histone H3. It forms a ubiquitin ligase complex in cooperation with the E2 enzyme UBE2E1/UBCH6. It thereby plays a central role in histone code and gene regulation. It is required for transcriptional activation of Hox genes. It is recruited to the MDM2 promoter, probably by being recruited by p53/TP53, and thereby acts as a transcriptional coactivator.

    更新時(shí)間:2025-03-02
    型號(hào):bsm-61100R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:123
  • bsm-61099R驅(qū)動(dòng)蛋白家族成員C1重組兔單抗

    The kinesins constitute a large family of microtubule-dependent motor proteins, which are responsible for the distribution of numerous organelles, vesicles and macromolecular complexes throughout the cell. Individual kinesin members play crucial roles in cell division, intracellular transport and membrane trafficking events including endocytosis and transcytosis. KIFC1 is a 673 amino acid protein that belongs to the kinesin-like family of proteins. KIFC1 localizes to the nucleus and contain

    更新時(shí)間:2025-03-02
    型號(hào):bsm-61099R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:134
  • bsm-61098RCD24重組兔單抗

    This gene encodes a sialoglycoprotein that is expressed on mature granulocytes and B cells and modulates growth and differentiation signals to these cells. The precursor protein is cleaved to a short 32 amino acid mature peptide which is anchored via a glycosyl phosphatidylinositol (GPI) link to the cell surface. This gene was missing from previous genome assemblies, but is properly located on chromosome 6. Non-transcribed pseudogenes have been designated on chromosomes 1, 15, 20, and Y. Al

    更新時(shí)間:2025-03-02
    型號(hào):bsm-61098R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:94
  • bsm-61097R纖維蛋白原γ鏈重組兔單抗

    Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.$nInvolvement in disease: Defects in FGG are a cause of thrombophilia.$nDefects in FGG are a cause of congenital afibrinogenemia (CAFBN). It is a rare autosomal recessive disorder characterized by complete absence of detectable fibrinogen.

    更新時(shí)間:2025-03-02
    型號(hào):bsm-61097R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:127
  • bsm-60930R花生四烯酸15脂氧合酶1重組兔單抗

    Lipoxygenases are a family of enzymes which dioxygenate unsaturated fatty acids, thus initiating lipoperoxidation of membranes and synthesis of signaling molecules, as well as inducing structural and metabolic changes in the cell. The Lox enzymes in mammals include 12-LO and 15-LO, which are classified with respect to their positional specificity of the deoxygenation of their most common substrate, arachidonic acid. The metabolism of arachidonic acid leads to the generation of biologically a

    更新時(shí)間:2025-03-02
    型號(hào):bsm-60930R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:101
  • bsm-54033R平滑肌肌球蛋白重鏈抗體

    The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end ove

    更新時(shí)間:2025-03-02
    型號(hào):bsm-54033R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:105
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