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RNA related

Products for  RNA related

  1. Cat.No. Product Name Information
  2. GB20108 2'-Amino-dATP Sugar modified nucleoside triphosphates, increases target affinity and nuclease stability while reducing immune response. 2'-Amino-dATP  Chemical Structure
  3. GB20093 2'-Azido-dGTP 2'-Azido-dGTP  Chemical Structure
  4. GB20101 2'-F-dTTP Sugar modified nucleoside triphosphates, increases nuclease stability. 2'-F-dTTP  Chemical Structure
  5. GB20118 2'-O-Methyl-2-Amino-ATP Sugar modified nucleoside triphosphates 2'-O-Methyl-2-Amino-ATP  Chemical Structure
  6. GB20110 2'-O-Methyl-5-methyl-UTP Sugar modified nucleoside triphosphates, increases target affinity and nuclease stability while reducing immune response. 2'-O-Methyl-5-methyl-UTP  Chemical Structure
  7. GB20130 2'-O-Methyl-ATP 2'-O-Methyl-ATP  Chemical Structure
  8. GB20127 2'-O-Methyl-CTP 2'-O-Methyl-CTP  Chemical Structure
  9. GB20124 2'-O-Methyl-GTP 2'-O-Methyl-GTP  Chemical Structure
  10. GB20152 2'-O-Methyl-N6-Methyl-ATP 2'-O-Methyl-N6-Methyl-ATP  Chemical Structure
  11. GB20121 2'-O-Methyl-UTP 2'-O-Methyl-UTP  Chemical Structure
  12. GB20115 2'-O-Methylpseudo-UTP Sugar modified nucleoside triphosphates, increases target affinity and nuclease stability while reducing immune response 2'-O-Methylpseudo-UTP  Chemical Structure
  13. GB20148 2-Amino-ATP 2-Amino-ATP  Chemical Structure
  14. GB20129 2-Thio-CTP

    Base modified ribonucleoside triphosphates.

    2-Thio-CTP  Chemical Structure
  15. GB20143 2-Thio-UTP

    Base modified ribonucleoside triphosphates. RNAs prepared from 2-Thio-UTP is less immunogenic as compared to unmodified RNA.

    2-Thio-UTP  Chemical Structure
  16. GB20099 3'-O-Methyl-ATP Sugar modified nucleoside triphosphates, used in epigenetics research. 3'-O-Methyl-ATP  Chemical Structure
  17. GB20098 3'-O-Methyl-CTP Sugar modified nucleoside triphosphates, used in epigenetics research. 3'-O-Methyl-CTP  Chemical Structure
  18. GB20097 3'-O-Methyl-GTP 3'-O-Methyl-GTP  Chemical Structure
  19. GB20096 3'-O-Methyl-UTP 3'-O-Methyl-UTP  Chemical Structure
  20. GB20114 4-Thio-UTP 4-Thio-UTP  Chemical Structure
  21. GB20160 5,6-Dihydro-5-Me-UTP 5,6-Dihydro-5-Me-UTP  Chemical Structure
  22. GB20132 5,6-Dihydro-UTP Base modified ribonucleoside triphosphates, used as acceptor substrate in dinucleoside polyphosphate synthesis. 5,6-Dihydro-UTP  Chemical Structure
  23. GB20103 5-Br-CTP Base modified ribonucleoside triphosphates, used in SELEX technique, provides thermal stability and nuclease resistance to aptamers. 5-Br-CTP  Chemical Structure
  24. GB20102 5-Br-UTP Base modified ribonucleoside triphosphates, used in SELEX technique, provides thermal stability and nuclease resistance to aptamers. 5-Br-UTP  Chemical Structure
  25. GB20151 5-Carboxy-UTP 5-Carboxy-UTP  Chemical Structure
  26. GB20134 5-Carboxymethylester-UTP 5-Carboxymethylester-UTP  Chemical Structure
  27. GB20153 5-Formyl-UTP 5-Formyl-UTP  Chemical Structure
  28. GB20158 5-hme-CTP 5-hme-CTP  Chemical Structure
  29. GB20159 5-hme-UTP 5-hme-UTP  Chemical Structure
  30. GB20155 5-Hydroxy-CTP 5-Hydroxy-CTP  Chemical Structure
  31. GB20149 5-Hydroxy-UTP 5-Hydroxy-UTP  Chemical Structure
  32. GB20141 5-Iodo-CTP 5-Iodo-CTP  Chemical Structure
  33. GB20137 5-Iodo-UTP 5-Iodo-UTP  Chemical Structure
  34. GB20142 5-Methoxy-CTP 5-Methoxy-CTP  Chemical Structure
  35. GB20146 5-Methoxy-UTP 5-Methoxy-UTP is an analogue of the naturally occurring uridine triphosphate (UTP). 5-Methoxy-UTP  Chemical Structure
  36. GB20105 5-Methyl-CTP 5-Methyl-CTP is a modified nucleoside triphosphate, commonly used to substitute the naturally occurring cytidine triphosphate (CTP) during in vitro mRNA synthesis. 5-Methyl-CTP  Chemical Structure
  37. GB20117 5-Methyl-UTP Base modified ribonucleoside triphosphates, used for in vitro transcription. 5-Methyl-UTP  Chemical Structure
  38. GB20120 5-MOM-CTP Base modified ribonucleoside triphosphates 5-MOM-CTP  Chemical Structure
  39. GB20119 5-MOM-UTP Base modified ribonucleoside triphosphates 5-MOM-UTP  Chemical Structure
  40. GB20126 6-Aza-CTP Base modified ribonucleoside triphosphates, used as substate in the study of specificity and nature of tRNA nucleotidyltransferase. 6-Aza-CTP  Chemical Structure
  41. GB20123 6-Aza-UTP Base modified ribonucleoside triphosphates, used in the study of UTP analogs on the activity of the norovirus and FCV ProPol enzymes. It is efficient in inhibiting FCV growth. 6-Aza-UTP  Chemical Structure
  42. GB20095 7-Deaza-ATP 7-Deaza-ATP  Chemical Structure
  43. GB20109 7-Deaza-GTP Base modified ribonucleoside triphosphates, used in the study of binding of the initiating GTP in transcription. 7-Deaza-GTP  Chemical Structure
  44. GB20145 8-Aza-ATP 8-Aza-ATP  Chemical Structure
  45. GB20104 8-Azido-ATP Base modified ribonucleoside triphosphates. 8-Azido-ATP  Chemical Structure
  46. GB20128 8-Oxo-ATP 8-Oxo-ATP  Chemical Structure
  47. GB20163 8-Oxo-GTP 8-Oxo-GTP  Chemical Structure
  48. GB20164 Aminoallyl-CTP Aminoallyl-CTP  Chemical Structure
  49. GB20113 Aminoallyl-UTP-X - Cy3 Aminoallyl-UTP-X - Cy3  Chemical Structure
  50. GB20107 Aminoallyl-UTP-X - Cy5 Aminoallyl-UTP-X - Cy5  Chemical Structure
  51. GB20106 Ara-ATP Sugar modified nucleoside triphosphates, when used with viral DNA polymerase, ara-ATP competes with dATP for incorporation into DNA leading to a termination of DNA synthesis. Ara-ATP  Chemical Structure
  52. GB20139 Ara-CTP Sugar modified nucleoside triphosphates, used as antiviral nucleotides. Ara-CTP  Chemical Structure
  53. GB20122 Ara-GTP Ara-GTP  Chemical Structure
  54. GB20135 Ara-UTP Sugar modified nucleoside triphosphates, used as antiviral nucleotides. Ara-UTP  Chemical Structure
  55. GB20100 ARCA Sodium ARCA Sodium  Chemical Structure
  56. GB20150 Biotin-16-UTP Biotin-16-UTP is a biotin-labeled nucleotide analog, which can be incorporated via a variety of RNA polymerases, including SP6, T3 and T7 RNA polymerases to form labeled RNA. Biotin-16-UTP  Chemical Structure
  57. GB20116 Cy3-UTP, 10mM Sodium Solution Cy3-UTP (Cyanine3-UTP) can replace UTP as the substrate of T7 RNA polymerase to produce labeled probes through in vitro transcription. Λexc=550nm/Λem=570nm.. Cy3-UTP, 10mM Sodium Solution  Chemical Structure
  58. GB20144 Cyanine 3-AA-CTP Cyanine 3-AA-CTP  Chemical Structure
  59. GB20140 Cyanine 5-AA-CTP Cyanine 5-AA-CTP  Chemical Structure
  60. GB20136 Cyanine 7-AA-UTP Cyanine 7-AA-UTP  Chemical Structure
  61. GB20147 Desthiobiotin-16-UTP Desthiobiotin-16-UTP  Chemical Structure
  62. GB20111 Fluorescein-12-UTP, 10mM Sodium Solution

    Fluorescein-12-UTP is a UTP analog of fluorescein, which can replace UTP for RNA labeling in in vitro transcription reactions.

    Fluorescein-12-UTP, 10mM Sodium Solution  Chemical Structure
  63. GB20125 Iso-GTP Iso-GTP  Chemical Structure
  64. GB20092 N1-Ethylpseudo-UTP N1-Ethylpseudo-UTP  Chemical Structure
  65. GB20156 N1-Methyl-2'-O-Methylpseudo-UTP N1-Methyl-2'-O-Methylpseudo-UTP  Chemical Structure
  66. GB20112 N1-Methyl-ATP Base modified ribonucleoside triphosphates, enhances protein expression and reduce immunogenicity. N1-Methyl-ATP  Chemical Structure
  67. GB20161 N1-Methylpseudo-UTP N1-methylpseudo-UTP is a nucleobase-modified nucleotide, used for synthesizing mRNA with reduced immunogenicity and improved stability. N1-Methylpseudo-UTP  Chemical Structure
  68. GB20091 N1-Methylpseudo-UTP (sodium salt) N1-methylpseudo-UTP is a nucleobase-modified nucleotide, used for synthesizing mRNA with reduced immunogenicity and improved stability. N1-Methylpseudo-UTP (sodium salt)  Chemical Structure
  69. GB20154 N1-Propyl-Pseudo-UTP N1-Propyl-Pseudo-UTP  Chemical Structure
  70. GB20162 N4-Methyl-CTP N4-Methyl-CTP  Chemical Structure
  71. GB20133 N6-Methyl-ATP N6-Methyl-ATP  Chemical Structure
  72. GB20094 O6-Methyl-GTP Base modified deoxynucleoside triphosphates, used in epigenetics research. O6-Methyl-GTP  Chemical Structure
  73. GB20131 Thieno-CTP Thieno-CTP  Chemical Structure
  74. GB20157 Thieno-GTP Thieno-GTP  Chemical Structure
  75. GB20138 Thieno-UTP Thieno-UTP  Chemical Structure

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