- 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 Agonists
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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 Inducers
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DNA/RNA Synthesis Degraders
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DNA/RNA Synthesis Controls
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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)
Related Products (2968)
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Antibodies (248)
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DNA/RNA Synthesis Isoform Comparison
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1-Benzyl-4-(bromomethyl)-1H-1,2,3-triazole
0 ImagesCat. No.: HY-W1058183CAS No.: 70380-30-21-Benzyl-4-(bromomethyl)-1H-1,2,3-triazole is a bromomethyl derivative that inhibits DNA synthesis in tumor cells and promotes the release of radioactivity from labeled nucleic acids. 1-Benzyl-4-(bromomethyl)-1H-1,2,3-triazole inhibits the growth of cancer cells in vitro with an ED50 of 2 μg/mL. It can be used in cervical cancer-related research. -
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T-2513
0 ImagesCat. No.: HY-125930CAS No.: 288247-87-0T-2513 is a selective topoisomerase I inhibitor. T-2513 binds covalently to and stabilizes the topoisomerase I-DNA complex and inhibits DNA replication and RNA synthesis, ultimately leading to cell death. -
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Vesleteplirsen sodium
0 ImagesCat. No.: HY-132585ASynonyms: SRP-5051 sodiumVesleteplirsen sodium (SRP-5051 sodium) is a peptide-conjugated morpholino oligonucleotide (PPMO) that mediates exon jumping molecular effects. Vesleteplirsen sodium targets exon 51 of the DMD gene pre-mRNA, remodeling the transcript splicing process, restoring the protein translation read frame, and generating internally truncated pseudodystrophy proteins. Vesleteplirsen sodium can be used for research related to Duchenne muscular dystrophy. -
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RNA binder 1
0 ImagesCat. No.: HY-172902CAS No.: 3105281-39-5RNA binder 1 (Compound 4b) is a blood-brain permeable RNA binder. RNA binder 1 can selectively bind to the G-quadruplex structure of the G4C2 repeat sequence RNA of the C9orf72 gene. RNA binder 1 significantly reduces the levels of toxic polypeptides poly(GA) and poly(GP) produced by the G4C2 repeat sequence in amyotrophic lateral sclerosis (ALS) patient-derived cells. RNA binder 1 has no significant effect on the antisense polypeptide poly(PR), showing selectivity for sense RNA. RNA binder 1 can be used in the study of ALS and frontotemporal dementia (FTD). -
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Cidofovir-13C,15N2 disodium
0 ImagesCat. No.: HY-167911SSynonyms: GS 0504-13C,15N2 disodium; HPMPC-13C,15N2 disodium; (S)-HPMPC-13C,15N2 disodiumCidofovir-13C,15N2 disodium (GS 0504-13C,15N2 disodium) is the 13C- and 15N-labeled Cidofovir disodium (HY-167911). Cidofovir sodium is an acyclic monophosphate nucleotide analogue and CMV inhibitor with antiviral activity. Cidofovir sodium inhibits cytomegalovirus (CMV) replication by selectively inhibiting viral DNA polymerase. Cidofovir sodium induces apoptosis and can be used in studies of AIDS cytomegalovirus retinitis, herpes, and cancer. Cidofovir sodium also has anti-orthopoxvirus and anti-variola activities. -
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Topoisomerase I-IN-18
0 ImagesCat. No.: HY-178373Topoisomerase I-IN-18, a derivative of Thiosemicarbazide (HY-Y0032), is a Topoisomerase I inhibitor. Topoisomerase I-IN-18 can disrupt DNA synthesis and transcription. Topoisomerase I-IN-18 inhibits tumor cell proliferation by inducing S-phase cell cycle arrest. Topoisomerase I-IN-18 can enhance mitochondria-mediated apoptosis, suppress cell migration, and increase intracellular Reactive Oxygen Species (ROS) levels. Topoisomerase I-IN-18 can increase p53 protein expression, γH2AX phosphorylation, upregulate Bax expression, downregulate Bcl-2 expression, and activate the caspase cascade. Topoisomerase I-IN-18 can be used for the study of lung cancer. -
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Anticancer agent 262
0 ImagesCat. No.: HY-170653Anticancer agent 262 (compound 3h) is a DNA intercalating anticancer agent, with an IC50 of 5.7 µM against A549 cancer cells. -
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PreQ1-DBCO
0 ImagesCat. No.: HY-185423PreQ1-DBCO is a strained cyclooctyne commonly used in click chemistry. PreQ1-DBCO undergoes TGT-catalyzed guanine base exchange in DNA oligonucleotide stem-loops to replace guanine. PreQ1-DBCO functionalizes custom DNA oligonucleotide sequences. DBCO-modified DNA oligonucleotides are conjugated with azide peptides via strain-promoted azide-alkyne click chemistry (SPAAC). PreQ1-DBCO can be used in studies of hemophilia B (Christmas disease). -
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ART558 (GMP)
0 ImagesCat. No.: HY-141520GCAS No.: 2603528-97-6ART558 (GMP) is ART558 (HY-141520) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. ART558 is a potent, selective and allosteric DNA polymerase theta (Polθ) inhibitor (IC50=7.9 nM). ART558 elicits BRCA-gene synthetic lethality and DNA damage. ART558 can be used for the research of cancer, such as breast cancer. -
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Alextatug
0 ImagesCat. No.: HY-P990727CAS No.: 2768264-93-1Alextatug is an anti-PABPC1 human IgG1 λ7 monoclonal antibody. -
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PROTAC CDK9 degrader-11
0 ImagesCat. No.: HY-170978CAS No.: 3039540-19-4PROTAC CDK9 degrader-11 is an orally active, selective CDK9 PROTAC degrader with a DC50 of 1.09 nM. PROTAC CDK9 degrader-11 recruits CRBN to form a ternary complex and degrades CDK9 via the ubiquitin-proteasome pathway, thereby inhibiting RNA polymerase II phosphorylation and downregulating the expression of anti-apoptotic and pro-oncogenic genes, ultimately inducing apoptosis. PROTAC CDK9 degrader-11 is suitable for research on small-cell lung cancer (SCLC). -
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Simeprevir-13C,d3
0 ImagesCat. No.: HY-10241SSynonyms: TMC435-13C,d3; TMC435350-13C,d3Simeprevir-13C,d3 is the 13C- and deuterium labeled Simeprevir. Simeprevir is an oral, potent and highly specific hepatitis C virus (HCV) NS3/4A protease inhibitor with a Ki of 0.36 nM. Simeprevir inhibits HCV replication with an EC50 of 7.8 nM. Simeprevir also potently suppresses SARS-CoV-2 replication and synergizes with Remdesivir. Simeprevir inhibits the main protease (Mpro) and the RNA-dependent RNA polymerase (RdRp) of SARS-CoV-2, and also modulates host immune responses. -
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DHX9-IN-15
0 ImagesCat. No.: HY-157607CAS No.: 2973398-27-3DHX9-IN-15 (287) is a RNA helicase DHX9 inhibitor, with an EC50 of 0.232 μM in DHX9 cellular target engagement. Used in cancer research. -
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- RP-4029
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dGTP
0 ImagesdGTP (2'-Deoxyguanosine-5'-triphosphate) is one of the precursors for DNA synthesis, and serves as a direct substrate for DNA replication and repair. dGTP is prone to oxidative damage; under the action of reactive oxygen species and other factors, dGTP is oxidized to form 8-oxo-dGTP. -
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S,S-DACH-Pt-SO4
0 ImagesCat. No.: HY-W783446CAS No.: 66900-71-8Synonyms: S,S-DACH-sulphS,S-DACH-Pt-SO4 is a platinum based drug. S,S-DACH-Pt-SO4 can cause cellular DNA damage. S,S-DACH-Pt-SO4 is toxic to sensitive cells but shows varying degrees of resistance to drug-resistant cells. S,S-DACH-Pt-SO4 can be used for cancer research. -
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20-5,14-HEDE-d2-2
0 ImagesCat. No.: HY-160099S2Synonyms: WIT003-d2-220-5,14-HEDE-d2 (WIT003-d2) is the deuterated-labeled 20-5,14-HEDE (HY-160099). 20-5,14-HEDE (WIT003) is an analog of 20-HETE. 20-5,14-HEDE activates PI3K/Akt signaling pathway, thereby exhibiting anti-apoptotic and cell survival promoting effects. 20-5,14-HEDE is the agonist for 20-HETE that increases intracellular Ca2+ concentrations, thereby enhancing vasoconstriction. -
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Tth DNA polymerase
0 ImagesCat. No.: HY-E70084CAS No.: 2409055-60-1Tth DNA polymerase is a DNA polymerase from T. thermophilus that can be used for DNA sequencing and polymerase chain reaction (PCR). -
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Dehydroeburiconic acid
0 ImagesCat. No.: HY-N21925CAS No.: 18449-25-7Dehydroeburiconic acid is a DNA polymerase α/β inhibitor, with IC50 values of 40.8 μM and 30.0 μM against calf DNA polymerase α and rat DNA polymerase β, respectively. Dehydroeburiconic acid can be used in studies related to lanostane-type triterpenoids and DNA polymerase. -
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Illudin B
0 ImagesCat. No.: HY-N16420CAS No.: 134857-03-7Illudin B is a DNA-targeting cytotoxin that forms interstrand DNA crosslinks via covalent binding, disrupting DNA replication and transcription. Illudin B induces cell cycle arrest and apoptosis, showing toxicity against multiple tumor cells (e.g., leukemia, breast, lung cancer). -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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