1. Signaling Pathways
  2. Cell Cycle/DNA Damage
  3. DNA/RNA Synthesis

DNA/RNA Synthesis

RNA synthesis, which is also called DNA transcription, is a highly selective process. Transcription by RNA polymerase II extends beyond RNA synthesis, towards a more active role in mRNA maturation, surveillance and export to the cytoplasm.

Single-strand breaks are repaired by DNA ligase using the complementary strand of the double helix as a template, with DNA ligase creating the final phosphodiester bond to fully repair the DNA.DNA ligases discriminate against substrates containing RNA strands or mismatched base pairs at positions near the ends of the nickedDNA. Bleomycin (BLM) exerts its genotoxicity by generating free radicals, whichattack C-4′ in the deoxyribose backbone of DNA, leading to opening of the ribose ring and strand breakage; it is an S-independentradiomimetic agent that causes double-strand breaks in DNA.

First strand cDNA is synthesized using random hexamer primers and M-MuLV Reverse Transcriptase (RNase H). Second strand cDNA synthesis is subsequently performed using DNA Polymerase I and RNase H. The remaining overhangs are converted into blunt ends using exonuclease/polymerase activity. After adenylation of the 3′ ends of DNA fragments, NEBNext Adaptor with hairpin loop structure is ligated to prepare the samples for hybridization. Cell cycle and DNA replication are the top two pathways regulated by BET bromodomain inhibition. Cycloheximide blocks the translation of mRNA to protein.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W579410
    DMT-2'-F-6-chloro-dA phosphoramidite
    DMT-2'-F-6-chloro-dA phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    DMT-2'-F-6-chloro-dA phosphoramidite
  • HY-183712
    Antibacterial agent 345
    Inhibitor
    Antibacterial agent 345 is a Ciprofloxacin (HY-B0356)-lipophilic derivative and is an antibacterial agent. Antibacterial agent 345 inhibits DNA gyrase and inhibits bacterial DNA replication and transcription. Antibacterial agent 345 inhibits bacterial biofilm formation. Antibacterial agent 345 can be used for the research of bacterial infections, such as Pseudomonas aeruginosa infection.
    Antibacterial agent 345
  • HY-201022
    5'-O-DMT-2'-F-5-MeO-U-3'-CE Phosphoramidite
    (2R,3R,4R,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-fluoro-5-(5-methoxy-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5'-O-DMT-2'-F-5-MeO-U-3'-CE Phosphoramidite
  • HY-168345A
    Ap4dT
    Inhibitor
    Ap4dT is an inhibitor for human adenylate kinase isozyme 1 (hAK1), that inhibits the ATP and ADP synthesis with IC50s of 42 μM and 38 μM.
    Ap4dT
  • HY-16965A
    TH287 hydrochloride
    Inhibitor
    TH287 hydrochloride is a potent and selective inhibitor of MTH1, with an IC50 of 0.8 nM. TH287 hydrochloride is highly selective towards MTH1, with no relevant inhibition of MTH2, NUDT5, NUDT12, NUDT14, NUDT16, dCTPase, dUTPase and ITPA at 100 μM. TH287 hydrochloride could act as a chemotherapeutic agent for cancer research.
    TH287 hydrochloride
  • HY-160704
    CMX-521
    CMX-521, a nucleoside analog, is a potent inhibitor for RNA-dependant RNA polymerase (RdRp) of norovirus. CMX-521 suppresses murine norovirus (MNV) and human norovirus.
    CMX-521
  • HY-17469R
    Gimeracil (Standard)
    Inhibitor
    Gimeracil (Standard) is the analytical standard of Gimeracil. This product is intended for research and analytical applications. Gimeracil, a component of an oral fluoropyrimidine derivative S-1, inhibits DNA DSB repair and is a potent inhibitor of DPYD (dihydropyrimidine dehydrogenase, DPD).
    Gimeracil (Standard)
  • HY-139101
    Guanosine 5'-triphosphate-5'-adenosine
    Guanosine 5'-triphosphate-5'-adenosine (GpppA), a 5′ cap analog, can be used for RNA synthesis in vitro. Guanosine 5'-triphosphate-5'-adenosine is a fluorescent substrate analog.
    Guanosine 5'-triphosphate-5'-adenosine
  • HY-10444R
    R-1479 (Standard)
    Inhibitor
    R-1479 (Standard) is the analytical standard of R-1479 (HY-10444). This product is intended for research and analytical applications. R-1479 (4'-Azidocytidine), a nucleoside analogue, is a specific inhibitor of RNA-dependent RNA polymerase (RdRp) of HCV. R-1479 inhibits HCV replication in the HCV subgenomic replicon system (IC50=1.28 μM). R-1479 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    R-1479 (Standard)
  • HY-185384
    SNA T amidite
    SNA T amidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    SNA T amidite
  • HY-182118
    tCnitro-CE phosphoramidite
    tCnitro-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    tCnitro-CE phosphoramidite
  • HY-N6936
    Sennidin A
    Sennidin A, isolated from the leaves of Cassia angustifolia, inhibits HCV NS3 helicase, with an IC50 of 0.8 μM. Sennidin A induces phosphorylation of Akt and glucose transporter 4 (GLUT4) translocation. Sennidin A stimulates the glucose incorporation.
    Sennidin A
  • HY-177335
    (R)-GNA-U phosphoramidite
    (R)-GNA-U phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    (R)-GNA-U phosphoramidite
  • HY-185041
    CHD1L-IN-2
    CHD1L-IN-2 is a CHD1L inhibitor and exhibits cytotoxicity against tumor cells.
    CHD1L-IN-2
  • HY-W048482A
    rU Phosphoramidite, 99%, ≤0.2%(K.F.)
    rU Phosphoramidite, 99%, ≤0.2%(K.F.) is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    rU Phosphoramidite, 99%, ≤0.2%(K.F.)
  • HY-182214
    TGC Trimer phosphoramidite
    TGC Trimer phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    TGC Trimer phosphoramidite
  • HY-182107
    dX-CE Phosphoramidite
    dX-CE Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    dX-CE Phosphoramidite
  • HY-153696
    MRL-436
    Inhibitor
    MRL-436 is a RNA polymerase inhibitor with antibacterial activity. MRL-436 exerts its antibacterial activity dependent on residue 622 of the RNA polymerase β' subunit and the RNAP ω subunit. MRL-436 inhibits Rifampicin (HY-B0272)-resistant RNA polymerase derivatives and exhibits antibacterial activity against Rifampicin-resistant strains.
    MRL-436
  • HY-182110
    5-Me-2'-Deoxyzebularine-CE phosphoramidite
    5-Me-2'-Deoxyzebularine-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
    5-Me-2'-Deoxyzebularine-CE phosphoramidite
  • HY-N11522A
    5-Methyluridine-5'-triphosphate trisodium
    5-Methyluridine-5'-triphosphate (5-Methyl-UTP) trisodium is a base modified ribonucleoside triphosphates, and can be used for in vitro transcription.
    5-Methyluridine-5'-triphosphate trisodium
Cat. No. Product Name / Synonyms Application Reactivity

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