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DNA(RNA) Synthesis

DNA(RNA) Synthesis

RNA synthesis, which is also called DNA transcription, is a highly selective process.Beyond RNA synthesis, RNA polymerase II transcription plays a more active role in the maturation, monitoring, and export of mRNA to the cytoplasm.

In order to fully repair the DNA after a single-strand break, DNA ligase constructs the final phosphodiester bond using the complementary strand of the double helix as a template.Substrates with RNA strands or mismatched base pairs near the ends of the nicked DNA are discriminated against by DNA ligases. Bleomycin (BLM) is a S-independent radiomimetic agent that damages DNA by creating free radicals that attack the C-4′ position in the deoxyribose backbone. This causes the ribose ring to open and strand breaks to occur.

M-MuLV Reverse Transcriptase (RNase H) and random hexamer primers are used to create first strand cDNA. The next step involves the use of DNA Polymerase I and RNase H to create second strand cDNA. Exonuclease/polymerase activity transforms the remaining overhangs into blunt ends. DNA fragments' 3′ ends are adenylated before being ligated with a NEBNext Adaptor with a hairpin loop structure to get the samples ready for hybridization. The two pathways that BET bromodomain inhibition most commonly affects are cell cycle and DNA replication. The translation of mRNA into proteins is inhibited by cycloheximide.

DNA(RNA) Synthesis related products

Structure Cat No. Product Name CAS No. Product Description
Quinizarin (1,4-二羟基蒽醌; 1,4-Dihydroxyanthraquinone) V34728 Quinizarin (1,4-Dihydroxyanthraquinone; 1,4-Dihydroxyanthraquinone) 81-64-1 Quinizarin (1,4-Dihydroxyanthraquinone) is a part of anti-cancer active molecules such as Doxorubicin, Daunorubicin, Adriamycin, etc.
Raltitrexed (ZD1694) V1473 Raltitrexed (ZD1694) 112887-68-0 Raltitrexed (formerly Thaltitrexed; ICID1694; TDX; ZD-1694; D1694; ICI-D1694; trade name: Tomudex),a quinazoline folate analog, is an approved antimetabolite anticancer drug used in cancer chemotherapy for treating colorectal cancer and malignant mesothelioma.
RdRP-IN-6 V81278 RdRP-IN-6 RdRP-IN-6 (compound 27) inhibits RNA dependent-RNA polymerase (RdRp) with an IC90 value of 14.1 μM.
RecQ helicase-IN-1 V84237 RecQ helicase-IN-1
Remdesivir (GS-5734) V4300 Remdesivir (GS-5734) 1809249-37-3 Remdesivir (GS-5734; Veklury) is an FDA approved drug for the treatment of 2019-nCoV (COVID-19 pandemic, CoronaVirus) infections requiring hospitalization.
Remdesivir O-desphosphate acetonide impurity V2203 Remdesivir O-desphosphate acetonide impurity 1191237-80-5 Remdesivir O-desphosphate acetonide impurity is a Remdesivirimpurity and an important intermediate to synthesize antiviral drug remdesivir.
RG3039 V4489 RG3039 1005504-62-0 RG3039 (also known as PF-06687859; PF 06687859), a member of a chemical series that was identified and optimized using an SMN2 promoter screen, is a novel, potent, orally bioavailable and brain-penetrant DcpS (decapping scavenger enzyme) inhibitor with an IC50 of 0.069 nM.
RG7800 V5680 RG7800 1449598-06-4 RG7800 (also known as RG-7800; RO6885247) is a potent and selective survival motor neuron 2 (SMN2) splicing modifier, which is currently being studies in human clinical trials for the treatment of Spinal Muscular Atrophy (SMA).
RG7800 tetrahydrochloride (RO6885247 tetrahydrochloride) V76558 RG7800 tetrahydrochloride (RO6885247 tetrahydrochloride) RG7800 HCl is an orally bioavailable SMN2 splicing modulator with EC1.5x values of 23 nM and 87 nM for SMN2 splicing and SMN protein, respectively.
Ribonuclease H (RNase H) V56159 Ribonuclease H (RNase H) 9050-76-4 Ribonuclease H is an enzyme that degrades the RNA portion of DNA-RNA hybrids.
Ribonuclease T1 (Rnase T1) V55111 Ribonuclease T1 (Rnase T1) 9026-12-4 Ribonuclease T1 (RNase T1), commonly used in biochemical research.
Rifampin (Rifampicin) V1468 Rifampin (Rifampicin) 13292-46-1 Rifampin (Rimactane; Arficin; Arzide; Rifampicin; Rifadin; Rimactane; Rimactan; Tubocin; Archidyn; Benemicin; Doloresum; Eremfat; Fenampicin; Sinerdol), an approved broad spectrum and semisynthetic antibiotic found in Streptomyces mediterranei, is mainly used to treat various bacterial infections such as TB-tuberculosis, leprosy,mycobacterium avium complex, and Legionnaires disease.
Rifaximin V1469 Rifaximin 80621-81-4 Rifaximin (BRN-3584528; L-105SV; Fatroximin; Normix; Rifacol; Rifaxidin; Rifaxin; Ritacol; Rifaximin; RCIFAX, Rifagut; Xifaxan; Zaxine) is an orally bioavailable and semi-synthetic RNA synthesis inhibitor used to treat travelers diarrhea caused by certain bacteria.
Rimantadine Hydrochloride V13787 Rimantadine Hydrochloride 1501-84-4 Rimantadine HCl (Flumadine Hydrochloride) is a bioactive oral medication that inhibits the influenza virus and can be used to treat and prevent influenza A fever.
RNA polymerase II-IN-1 V75896 RNA polymerase II-IN-1 2891451-07-1 RNA polymerase II-IN-1 (compound 19iv) is an amanitaxin that can inhibit RNA polymerase II (Pol II) with IC50 of 36.66 nM.
RNA splicing modulator 1 V55157 RNA splicing modulator 1 2726461-38-5 RNA splicing modulator 1 (compound 233) is an RNA splicing modulator with AC50 value <100 nM.
RNA splicing modulator 2 V55155 RNA splicing modulator 2 2726461-41-0 RNA splicing modulator 2 (compound 256) is an RNA splicing modulator.
RNA splicing modulator 3 V55115 RNA splicing modulator 3 2726461-43-2 RNA splicing modulator 3 (compound 236) is an RNA splicing modulator with AC50 value <100 nM.
RNase III V81317 RNase III RNase III is a double-stranded RNA (dsRNA)-specific endonuclease produced by Escherichia coli expressing the RNase III gene.
RNaseL-IN-1 V81318 RNaseL-IN-1 RNase L-IN-1 (compound 17a) is an inhibitor (blocker/antagonist) of RNase L or ribonuclease L.
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