- 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 Substrates
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DNA/RNA Synthesis Ligands
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DNA/RNA Synthesis Related Products (2928)
Related Products (2928)
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Antibodies (248)
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DNA/RNA Synthesis Isoform Comparison
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2'-OMe-C Phosphoramidite
0 ImagesCat. No.: HY-185292CAS No.: 138906-72-62'-OMe-C Phosphoramidite, a phosphoramidite, is used in the synthesis of oligonucleotides. -
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Nadifloxacin-d5
0 ImagesCat. No.: HY-B0506S1Synonyms: OPC7251-d5Nadifloxacin-d5 (OPC7251-d5) is deuterium labeled Nadifloxacin (HY-B0506). Nadifloxacin (OPC7251) is a broad-spectrum quinolone antibiotic. Nadifloxacin inhibits bacterial DNA gyrase and topoisomerase IV, interfering with DNA replication. It also suppresses the production of proinflammatory cytokines (such as IL-1α, IL-6, and IL-8). Nadifloxacin exhibits antibacterial activity against various pathogens, including Propionibacterium acnes and Staphylococcus aureus. Nadifloxacin also exhibits anti-inflammatory activity. Nadifloxacin can be used in the research of skin infections such as acne vulgaris, folliculitis, and impetigo. -
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6-NED Phosphoramidite
0 ImagesCat. No.: HY-185992CAS No.: 1414264-37-16-NED Phosphoramidite is a phosphoramidite reagent used in the solid-phase synthesis of oligonucleotides (DNA/RNA) to incorporate the 6-NED fluorescent moiety, thereby yielding fluorescently labeled oligonucleotides. -
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HEX-dT Phosphoramidite
0 ImagesCat. No.: HY-185989AHEX-dT Phosphoramidite is a phosphoramidite reagent used in oligonucleotide synthesis to incorporate a HEX-labeled deoxythymidine into DNA or RNA sequences. -
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CL 232468
0 ImagesCat. No.: HY-116662CAS No.: 96555-65-6CL 232468 is an immunosuppressive agent. -
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Daunorubicin hydrochloride (Standard)
0 ImagesSynonyms: Daunomycin hydrochloride (Standard); RP 13057 hydrochloride (Standard); Rubidomycin hydrochloride (Standard)Daunorubicin (hydrochloride) (Standard) is the analytical standard of Daunorubicin (hydrochloride). This product is intended for research and analytical applications. Daunorubicin (Daunomycin) hydrochloride is a topoisomerase II inhibitor with potent anti-tumor activity. Daunorubicin hydrochloride inhibits DNA and RNA synthesis. Daunorubicin hydrochloride is a cytotoxin that inhibits cancer cell viability and induces apoptosis and necrosis. Daunorubicin hydrochloride is also an anthracycline antibiotic. Daunorubicin hydrochloride can be used in the research of infection and variety of cancers, including leukemia, non-Hodgkin lymphomas, Ewing's sarcoma, Wilms' tumor. -
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Arecaidine-propargyl ester
0 ImagesCat. No.: HY-183853CAS No.: 35516-99-5Arecaidine-propargyl ester is a selective M2 muscarinic receptor agonist with blood-brain barrier permeability, with a pKi of 5.91 for hm1, 7.06 for hm2, 6.07 for hm3, 6.01 for hm4, and 6.03 for hm5. Arecaidine-propargyl ester stimulates central and peripheral muscarinic receptors. Arecaidine-propargyl ester increases intracellular ROS, induces DNA damage and Apoptosis, and upregulates the expression of MnSOD and SIRT1. Arecaidine-propargyl ester reduces sympathetic nerve outflow, induces dose-dependent hypotension, and triggers negative chronotropic effects at high peripheral doses. Arecaidine-propargyl ester can be used in research related to Alzheimer's disease and glioblastoma. -
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Tezacitabine (Standard)
0 ImagesCat. No.: HY-106014RCAS No.: 130306-02-4Tezacitabine (Standard) is the analytical standard of Tezacitabine (HY-106014). This product is intended for research and analytical applications. Tezacitabine is a cytostatic and cytotoxic antimetabolite and a nucleoside analogue. Tezacitabine irreversibly inhibits the ribonucleotide reductase and interferes with DNA replication and repair. Tezacitabine effectively induces cells apoptotic. Tezacitabine has the potential for leukemias and solid tumors (carcinomas) treatment. -
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Tocopherol-TEG-MMTr-PEG3-phosphoramidite
0 ImagesCat. No.: HY-W7149542-Cyanoethyl (1-(3-methoxyphenyl)-1-(4-methoxyphenyl)-1-phenyl-14-((2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl)oxy)-2,6,9,12-tetraoxatetradecan-4-yl) diisopropylphosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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O4-triazolyl-dU-CE phosphoramidite
0 ImagesCat. No.: HY-182114CAS No.: 109389-31-3O4-triazolyl-dU-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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BQ-650-dT Phosphoramidite
0 ImagesCat. No.: HY-W1061568CAS No.: 905554-46-3BBQ-650-dT Phosphoramidite is a biochemical reagent that can introduce BBQ-650 quenching groups at sites within oligonucleotide sequences or at the 5' end. BBQ-650-dT Phosphoramidite can be used in bioimaging, nucleic acid fluorescent probes, and other related research. -
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TH588 (Standard)
0 ImagesCat. No.: HY-12814RCAS No.: 1609960-31-7TH588 (Standard) is the analytical standard of TH588. This product is intended for research and analytical applications. TH588 is first-in-class nudix hydrolase family inhibitor that potently and selectively engage and inhibit the MTH1 (IC50= 5 nM). -
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DNA gyrase/Topo IV-IN-2
0 ImagesCat. No.: HY-175539DNA gyrase/Topo IV-IN-2 (Compound AK19) is an antibacterial agent with IC50 values of 0.783 μM and 7.136 μM against E. coli DNA gyrase and topoisomerase IV, respectively. DNA gyrase/Topo IV-IN-2 exhibits broad-spectrum antibacterial efficacy against both Gram-positive and Gram-negative pathogens. DNA gyrase/Topo IV-IN-2 can inhibit the biofilms of B. subtilis and MRSA, with an MIC of 1.9 μM against both B. subtilis and MRSA. DNA gyrase/Topo IV-IN-2 can be used in research related to anti-drug-resistant bacterial drugs. -
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Cyanine 5.5 phosphoramidite
0 ImagesCat. No.: HY-182187CAS No.: 916753-58-7Cyanine 5.5 phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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PC Spacer phosphoramidite
0 ImagesCat. No.: HY-182159CAS No.: 653575-45-2PC Spacer phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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Crisnatol (Standard)
0 ImagesSynonyms: BWA770U (Standard)Crisnatol (Standard) is the analytical standard of Crisnatol. This product is intended for research and analytical applications. Crisnatol (BWA770U) is an orally active and anticancer agent, and a member of the arylmethylaminopropanediol class of DNA intercalators. Crisnatol shows in vitro cytotoxicity against human breast cancer cells, but not normal human skin fibroblasts. -
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Pefloxacin mesylate (Standard)
0 ImagesSynonyms: Pefloxacinium mesylate (Standard)Pefloxacin mesylate (Standard) (Pefloxacinium mesylate (Standard)) is the analytical standard of Pefloxacin mesylate (HY-B0147A). This product is intended for research and analytical applications. Pefloxacin (Pefloxacinium) mesylate is a broad spectrum antibiotic. Pefloxacin blocks DNA replication by inhibiting DNA gyrase. Pefloxacin mesylate inhibits DNA relaxation catalyzed by topoisomerase I with an IC50 of 45 μg/mL. Pefloxacin mesylate exhibits antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, and Bacteroides fragilis with MIC90s of 0.12, 4, and 16 mg/L, respectively. Pefloxacin mesylate has anti-Plasmodium yoelii infection activity. Pefloxacin mesylate increase UVA-induced edema and immunesuppression. Pefloxacin mesylate can be used for infection studies. -
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m7GpppAmpG
0 ImagesCat. No.: HY-145974CAS No.: 62858-30-4Synonyms: m7G(5')ppp(5')(2'OMeA)pG -
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- 2'-Fluoro guanosine (n-acetyl) P-methyl phosphoramidite
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5-I-U-CE Phosphoramidite
0 ImagesCat. No.: HY-182207CAS No.: 1645262-08-35-I-U-CE Phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides. -
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