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        5-Methylcytidine-5'-Triphosphate

        簡(jiǎn)要描述:5-甲基胞苷-5-三磷酸鹽是TRILINK公司產(chǎn)品,用于干細(xì)胞研究用

        • 產(chǎn)品型號(hào):5-甲基胞苷-5-三磷酸鹽
        • 廠商性質(zhì):代理商
        • 更新時(shí)間:2025-12-30
        • 訪  問(wèn)  量:4419

        詳細(xì)介紹

        5-甲基胞苷-5-三磷酸鹽是TRILINK公司產(chǎn)品,用于干細(xì)胞研究用,5-methyl-ctp

        Synonyms]
        5-methyl-dCTP
        5-methyldeoxycytidine triphosphate
        CPD-1094
        5-methyl deoxycytidine-5'-triphosphate
        5-methyl-2'-deoxycytidine-5'-triphosphate
        cytidine 5'-(tetrahydrogen triphosphate), 2'-deoxy-5-methyl-
        [[[5-[(4-amino-5-methyl-2-oxo-1H-pyrimidin-1-yl)]-3-hydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphinoyl]oxy-hydroxy-phosphinoyl]oxyphosphonic acid

        [Structure]
         

        5-methyl-dCTP ,5-methyldeoxycytidine triphosphate ,CPD-1094,5-methyl d


        [ Properties Computed from Structure]
         

        Molecular Weight 481.183503 [g/mol]
        Molecular Formula C10H18N3O13P3
        XLogP -5.9
        H-Bond Donor 6
        H-Bond Acceptor 14
        Rotatable Bond Count 8
        Tautomer Count 3
        Exact Mass 481.005247
        MonoIsotopic Mass 481.005247
        Topological Polar Surface Area 248
        Heavy Atom Count 29
        Formal Charge 0
        Complexity 868
        Isotope Atom Count 0
        Defined Atom StereoCenter Count 0
        Undefined Atom StereoCenter Count 3
        Defined Bond StereoCenter Count 0
        Undefined Bond StereoCenter Count 0
        Covalently-Bonded Unit Count 1

        Description
        5-Methyl-dCTP is widely used for construction of cDNA libraries
         
        Incorporation of 5-Methyl-dCTP
        M-MuLV Reverse Transcriptase
        Klenow Fragment of DNA Polymerase I
        Sequenase DNA Polymerase
        (Taq Polymerase, Vent) *
        Incorporation of Hg-dCTP
        DNA Polymerase I

        References to 5-Methyl-dCTP
        Lefaucheur et al. (1998) Evidence for three adult fast myosin heavy chain isoforms in type II skeletal muscle fibers in pigs. J. Anim. Sci. 76:1584.
        Nelson et al. (1993) Restriction endonuclease cleavage of 5-methyl-deoxycytosine hemimethylated DNA at high enzyme-to-substrate ratios. Nucl. Acids Res. 21 (3):681.
        Asamizu et al. (1999) A large scale structural analysis of cDNAs in a unicellular green alga, Chlamydomonas reinhardtii. I. Generation of 3433 non-redundant expressed sequence tags. DNA Research 6:369.
        * Wong et al. (1991) PCR with 5-methyl-dCTP replacing dCTP. Nucl. Acids Res. 19 (5):1081.
        Reference to Hg-dCTP
        Banfalvi et al. (1995) Effect of mercury substitution of DNA on its susceptibility to cleavage by restriction endonucleases. DNA Cell Biol. 14 (5):445.
         

         

        N-1014-1 5-Methylcytidine-5'-TP 1umole 1317.5
        N-1014-10 5-Methylcytidine-5'-TP 10umoles 10625
        N-1014-5 5-Methylcytidine-5'-TP 5umoles 6205

         

        Reference(s)
        Kariko K, Muramatsu H, Ludwig J, Weissman D. Generating the optimal mRNA for therapy: HPLC purification eliminates immune activation and improves translation of nucleoside-modified, protein encoding mRNA. (2011) Nucleic Acids Research.
                 
        Kormann M, Hasenpusch G, Aneja M, et al. Expression of therapeutic proteins after delivery of chemically modified mRNA in mice. (2011) Nature Biotechnology 29:154–157.
                 
        Anderson, B., Muramatsu, H., Nallagatla, S.R., Bevilacqua, P.C., Sansing, L.H., Weissman, D. & Kariko, K. Incorporation of pseudouridine into mRNA enhances translation by dimishing PKR activation (2010) Nucleic Acids Research, 38(17): 5884-5892.
                 
        Warren et al., Highly Efficient Reprogramming to Pluripotency and Directed Differentiation of Human Cells with Synthetic Modified mRNA, Cell Stem Cell (2010), doi:10.1016/j.stem.2010.08.012.
                 
        Kariko K, Muramatsu H, Welsh F, et al. Incorporation of Pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability. (2008) Molecular Therapy (16)11: 1833-1840.
                 
        Kariko, K., Buckstein, M., Ni, H. & Weissman, D. Suppression of RNA Recognition by Toll-like Receptors: The Impact of Nucleoside Modifiation and the Evolutionary Origin of RNA (2005). Immunity, 23(2), 165-175.
                 
        Lefmann M, et al. Novel Mass Spectrometry-based tool for genotypic identification of mycobacteria. (2004) Journal of Clinical Microbiology, 42(1): 339-346.
                 
        Hartmer R, Storm N, Boecker S, Rodi CP, Hillenkamp F, Jurinke C, van den Boom D. RNase T1 mediated base-specific cleavage and MALDI-TOF MS for high-throughput comparative sequence analysis. (2003) Nucleic Acids Res., 31(9): e47.
                 
        Nguyen A, Zhao C, Dorris D, Mazumder A. Quantitative assessment of the use of modified nucleoside triphosphates in expression profiling: differential effects on signal intensities and impacts on expression ratios. (2002) BMC Biotechnology, 2(1): 14.
                 
        Van Rompay AR, Norda A, Linden K, Johansson M, Karlsson A. Phosphorylation of uridine and cytidine nucleoside analogs by two human uridine-cytidine kinases. (2001) Mol Pharmacol., 59(5): 1181-6.
                 

         

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