- Signaling Pathways
- Cell Cycle/DNA Damage
- 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.
DNA/RNA Synthesis Isoform Specific Products
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DNA/RNA Synthesis Inhibitors
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DNA/RNA Synthesis Antagonists
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DNA/RNA Synthesis Activators
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DNA/RNA Synthesis Chemicals
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DNA/RNA Synthesis Substrates
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DNA/RNA Synthesis Ligands
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DNA/RNA Synthesis Related Products (2968)
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Antibodies (248)
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DNA/RNA Synthesis Isoform Comparison
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Idarubicin hydrochloride (Standard)
0 ImagesCat. No.: HY-17381RCAS No.: 57852-57-0Synonyms: 4-Demethoxydaunorubicin hydrochloride (Standard)Idarubicin (hydrochloride) (Standard) is the analytical standard of Idarubicin (hydrochloride). This product is intended for research and analytical applications. Idarubicin hydrochloride is an anthracycline antileukemic agent. It inhibits the topoisomerase II interfering with the replication of DNA and RNA transcription. Idarubicin hydrochloride inhibits the growth of bacteria and yeasts. -
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2'-O-Methylguanosine-5'-O-triphosphate sodium
0 ImagesCat. No.: HY-174162ASynonyms: 2'-Methyl GTP sodium2'-O-Methylguanosine-5'-O-triphosphate sodium (2'-Methyl GTP sodium), a methylated derivative of Guanosine 5'-triphosphate (HY-W010737), is a HCV NS5B RNA-dependent RNA polymerase inhibitor. 2'-O-Methylguanosine-5'-O-triphosphate sodium is a nucleotide competitor of GTP and acts as a chain terminator to inhibit RNA synthesis. 2'-O-Methylguanosine-5'-O-triphosphate sodium can be used for HCV infections research. -
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5'-DMTr-TFA-ap-dU-3'-CE-Phosphoramidite
0 ImagesCat. No.: HY-W784555CAS No.: 120016-98-0(2R,3S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-5-(3-(2,2,2-trifluoroacetamido)prop-1-yn-1-yl)-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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3'-Deoxy-5'-O-(4,4'-dimethoxytrityl)-3'-fluoro uridine-2'-CED-phosphoramidite
0 ImagesCat. No.: HY-154608CAS No.: 129015-63-03’-Deoxy-5’-O-(4,4’-dimethoxytrityl)-3’-fluoro uridine-2’-CED-phosphoramidite is a phosphorite monomer that can be used in the synthesis of oligonucleotides. -
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Enoxacin-d8 hydrate
0 ImagesCat. No.: HY-B0268S2Enoxacin-d8 (hydrate) is deuterium labeled Enoxacin. Enoxacin (AT 2266), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC50=126 μg/ml) and topoisomerase IV (IC50=26.5 μg/ml). Enoxacin is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin has potent activities against gram-positive and -negative bacteria. Enoxacin is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing. -
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5'-O-DMT-3'-Me-dG(dmf)-CE phosphoramidite
0 ImagesCat. No.: HY-W714978(2R,3S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2-(((E)-(dimethylamino)methylene)amino)-5-methyl-4-oxo-3,4-dihydro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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2-Amino-dA-CE phosphoramidite
0 ImagesCat. No.: HY-164810CAS No.: 1432451-35-82-Amino-dA-CE Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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- 5'-O-DMTr-dU-methyl phosphonamidite
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5'-O-DMT-3'-5-Chloro-dC (Ac)-CE phosphoramidite
0 ImagesCat. No.: HY-W714981CAS No.: 1356140-67-4(2R,3S,5R)-5-(4-Acetamido-5-chloro-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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dNaMTP
0 ImagesCat. No.: HY-157263CAS No.: 1117893-11-4dNaMTP is an unnatural nucleoside triphosphate. dNaMTP forms an unnatural base pair (UBP) and expands the genetic alphabet. -
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DMTr-3'-O-TBDMS-rC(Ac)-CE Phosphoramidite
0 ImagesCat. No.: HY-W784561CAS No.: 237060-94-5(2S,3S,4S,5S)-5-(4-Acetamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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DMT-2'O-MOE-rG(ib) Phosphoramidite (Standard)
0 ImagesCat. No.: HY-104014RCAS No.: 251647-55-9DMT-2'O-MOE-rG(ib) Phosphoramidite (Standard) is the analytical standard of DMT-2'O-MOE-rG(ib) Phosphoramidite (HY-104014). This product is intended for research and analytical applications. DMT-2'O-MOE-rG(ib) Phosphoramidite belongs to cyanoethyl-protected nucleoside phosphoramidites. DMT-2'O-MOE-rG(ib) Phosphoramidite is a derivative of nucleotide and guanosine. DMT-2'O-MOE-rG(ib) Phosphoramidite can be used for the stereochemical synthesis of phosphorothioate oligonucleotides. -
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DMT-2'O-TC-rC(ac) phosphoramidite
0 ImagesCat. No.: HY-W1121775CAS No.: 1219089-87-8DMT-2'O-TC-rC(ac) Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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7-Deaza-dA(Bz)-CE phosphoramidite
0 ImagesCat. No.: HY-W1121780CAS No.: 107134-59-87-Deaza-dA(Bz)-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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2'-OPEG(N-TFA)-rG(N-iBu) Phosphoramidite
0 ImagesCat. No.: HY-188040CAS No.: 1953146-88-72'-OPEG(N-TFA)-rG(N-iBu) Phosphoramidite is a 2'-OPEG-modified guanosine phosphoramidite containing an N-TFA-protected PEG functionality and an N-isobutyryl (N-iBu)-protected guanine nucleobase. It is a modified RNA phosphoramidite building block suitable for incorporating a 2'-OPEG-modified guanosine unit into oligonucleotides during phosphoramidite-based synthesis. -
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(R)-Adibelivir
0 ImagesSynonyms: (R)-IM-250(R)-Adibelivir ((R)-IM-250) is a blood-brain barrier-permeable HSV helicase-primase inhibitor. (R)-Adibelivir specifically inhibits the activity of the HSV UL5-UL52-UL8 helicase-primase complex. (R)-Adibelivir affects viral reactivation and significantly reduces the reactivation capacity of latent neuronal HSV reservoirs. (R)-Adibelivir can be used in studies related to herpes simplex virus infection, herpes encephalitis, neonatal herpes, and other related conditions. -
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NusB-NusE interaction IN-1
0 ImagesCat. No.: HY-123722CAS No.: 125966-81-6NusB-NusE interaction IN-1 is a NusB-NusE protein-protein interaction inhibitor and growth inhibitor with a Bacillus subtilis IC50 of 6.1 μM.NusB-NusE interaction IN-1 inhibits growth of Gram-positive Bacillus subtilis.NusB-NusE interaction IN-1 inhibits growth of Gram-negative Escherichia coli. -
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- 5'(E)-VP-2'-OMe-Bz-C Phosphoramidite
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HSV-1/HSV-2-IN-3
0 ImagesCat. No.: HY-174252CAS No.: 3016396-78-1HSV-1/HSV-2-IN-3 inhibits the herpes-simplex-virus (HSV) helicase-primase complex, blocking the coordinated DNA-unwinding and primer-synthesis steps required for viral genome replication. HSV-1/HSV-2-IN-3 exhibits an EC50 of 7.0 nM against HSV-2 in a gD-immunofluorescence cell assay containing 2 % FBS and 57.5 nM when 10 % human serum is present. HSV-1/HSV-2-IN-3 achieves an EC50 of 1.1 nM in a qPCR replication assay. HSV-1/HSV-2-IN-3 shows strong selectivity over human carbonic-anhydrase off-targets (IC50 ≈ 2.9 µM for hCA II and > 35 µM for hCA I). HSV-1/HSV-2-IN-3 can be studied in anti-HSV research. -
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Amotosalen hydrochloride (Standard)
0 ImagesCat. No.: HY-107004ARCAS No.: 161262-45-9Synonyms: S-59 (Standard)Amotosalen hydrochloride (Standard) (S-59 (Standard)) is the analytical standard of Amotosalen (hydrochloride) (HY-107004A). This product is intended for research and analytical applications. Amotosalen hydrochloride (S-59) is a light-activated, DNA-, RNA-crosslinKing psoralen compound, which is used to neutralise pathogens. Light-activated Amotosalen binds and permanently crosslinks DNA, preventing replication and thus stopping proliferation of donor T cells. Amotosalen can be used for the study of blood system pathogen reduction technology and graft-versus-host disease (GVHD). -
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