- 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 Modulators
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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 (2965)
Related Products (2965)
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Antibodies (248)
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DNA/RNA Synthesis Isoform Comparison
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Fmoc-PNA-Abasic(Boc)-OH
0 ImagesCat. No.: HY-160513CAS No.: 511534-99-9Fmoc‑PNA‑Abasic(Boc)‑OH is a synthetic peptide nucleic acid modified with Fmoc and Boc protecting groups. Fmoc‑PNA‑Abasic(Boc)‑OH can be used in molecular biology research. -
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Skim Milk powder
0 ImagesCat. No.: HY-182832Synonyms: Dry skim milk; Non-fat milk solids; Skimmed milk powderSkim Milk powder (Dry skim milk) is an orally effective, dairy-derived non-fat milk solid powder. Skim Milk powder serves as a nutrient source in microbial culture media and can also be used for blocking procedures in WB assays. Skim Milk powder protects zebrafish sperm from oxidative stress, DNA damage, membrane disruption and morphological abnormalities during cryopreservation, and improves their survival rate. After undergoing high Maillard reaction during moist-heat storage, Skim Milk powder exhibits negative metabolic activities such as inhibiting GLP-1/GIP and promoting intestinal inflammation. Skim Milk powder can be used in studies related to intestinal inflammation, diabetes and obesity. -
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Miboplatin
0 ImagesCat. No.: HY-W583012CAS No.: 103775-75-3Synonyms: DWA-2114RMiboplatin (DWA-2114R), a platinum compound, is a DNA synthesis inhibitor. Miboplatin reduces its template activity for prokaryotic and eukaryotic DNA polymerases. -
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SQS-IN-1
0 ImagesCat. No.: HY-178158CAS No.: 2306302-57-6SQS-IN-1 is a squalene synthase (SQS) inhibitor. SQS-IN-1 exhibits potent and broad-spectrum anti-proliferative effects on both mouse and human lung cancer cell lines. SQS-IN-1 inhibits DNA replication and the cell cycle, causing mitochondrial hyperpolarization and inducing cell apoptosis. SQS-IN-1 inhibits cell migration and invasion. SQS-IN-1 can be used to the study of lung cancer. -
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HBV-IN-22
0 ImagesCat. No.: HY-146394CAS No.: 2338573-94-5 -
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Kukoamine B-d5 dihydrochloride
0 ImagesCat. No.: HY-N2393SKukoamine B, a spermine alkaloid, is a potent dual LPS and CpG DNA inhibitor with Kd values of 1.23 µM and 0.66 µM, respectively. Kukoamine B exerts anti-inflammatory, anti-diabetic, anti-oxidant, anti-osteoporotic and neuroprotective effects. Kukoamine B has the potential for the study of sepsis. . -
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FLDP-5
0 ImagesCat. No.: HY-150791CAS No.: 950665-12-0FLDP-5 is a blood-brain barrier (BBB) penetrant curcuminoid analogues. FLDP-5 can induce production of ROS (Reactive Oxygen Species), DNA damage and cell cycle S phase arrest. FLDP-5 exhibits highly potent tumour-suppressive effects with anti-proliferative and anti-migratory activities on LN-18 cells. -
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Ara-ATP trisodium
0 ImagesCat. No.: HY-134031ACAS No.: 71997-34-7Ara-ATP trisodium is an ATP-competitive poly (A) polymerase (poly (A) polymerase) inhibitor with a Ki value of 4 μM for the chromatin-bound form and a Ki value of 60 μM for the nucleoplasmic (free) form. Ara-ATP trisodium blocks pre-mRNA 3' end processing by inhibiting endonucleolytic cleavage, poly (A) addition, and the formation of cleavage and polyadenylation-specific RNA-protein complexes. Ara-ATP trisodium selectively inhibits initial polyadenylation rather than poly (A) elongation. Ara-ATP trisodium is used in the study of viral infections. -
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DMT-dI Phosphoramidite
0 ImagesPhosphoramidite is a modified phosphoramidite monomer used for the oligonucleotide synthesis. -
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Halofuginone hydrochloride (Standard)
0 ImagesCat. No.: HY-N1584BRCAS No.: 1217623-74-9Synonyms: RU-19110 hydrochloride (Standard)Halofuginone hydrochloride (Standard) (RU-19110 hydrochloride (Standard)) is the analytical standard of Halofuginone hydrochloride (HY-N1584B). This product is intended for research and analytical applications. Halofuginone hydrochloride (RU-19110 hydrochloride), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM. Halofuginone hydrochloride is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity. Halofuginone hydrochloride is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca2+ channels. Halofuginone hydrochloride has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects. -
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Influenza virus PA (46-54)
0 ImagesCat. No.: HY-P5478CAS No.: 318273-25-5Influenza virus PA (46-54) is a biological active peptide. (HLA-A*0201 restricted epitope from influenza virus RNA polymerase subunit, PA (46-54).) -
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M7G (3'-OMe-5') pppA (2'-OMe)
0 ImagesCat. No.: HY-147339CAS No.: 3047739-39-6M7G (3'-OMe-5') pppA (2'-OMe) is a modified cap analog. M7G (3'-OMe-5') pppA (2'-OMe) enhances the stability and translation efficiency of mRNA by maintaining the correct orientation of the mRNA cap, promoting cap-dependent translation initiation, and mimicking the Cap-1 structure to reduce immunogenicity. M7G (3'-OMe-5') pppA (2'-OMe) can be used in molecular biology research, vaccine development, and gene therapy applications. -
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Boc-PNA-U-OH
0 ImagesCat. No.: HY-P11679CAS No.: 149500-74-3Boc-PNA-U-OH is a protected peptide nucleic acid (PNA) monomer containing a uracil base, designed for solid-phase peptide synthesis (SPPS) using the Boc/Z protection strategy. Boc-PNA-U-OH acts as a building block in creating PNA oligomers that are neutral, stable, and used for antisense/antigene applications. -
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hDHODH-IN-12
0 ImagesCat. No.: HY-149877hDHODH-IN-12 is a potent DHODH inhibitor with an IC50 value of 0.421 μM. DHODH is the rate-limiting enzyme in the de novo synthesis of pyrimidine which is essential in DNA/RNA Synthesis. hDHODH-IN-12 is present in the inner membrane of human mitochondria.hDHODH-IN-12 can be used for the research of lung cancer. -
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YM-534
0 ImagesCat. No.: HY-122157CAS No.: 95923-66-3YM-534, an imidazole compound, is an anti-cancer agent. YM-534 inhibits HL-60 cells with an IC50 of 2.5 μM. YM-534 retards the processing of preribosomal to ribosomal RNA of HL-60 cells. YM-534 can be used for the study of promyelocytic leukemia. -
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CRX 527
0 ImagesCat. No.: HY-155801CAS No.: 216014-14-1CRX 527 is a TLR4 agonist. CRX 527 activates the MyD88-dependent, TRIF-dependent, and TRAF6/NF-κB signaling pathways downstream of TLR4, mimics lipid A, and regulates antigen processing and presentation by dendritic cells. CRX 527 stimulates innate immune responses and enhances vaccine efficacy. CRX 527 maintains the structural integrity of hematopoietic tissues, spleen and intestine, alleviates radiation-induced damage, preserves intestinal homeostasis, and inhibits apoptosis, inflammatory responses, oxidative stress and DNA damage. CRX 527 can be used in the research of acute radiation syndrome, melanoma, HPV-related tumors and intracerebral hemorrhage. -
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3'-P-dCTP sodium
0 ImagesCat. No.: HY-1586753'-P-dCTP sodium is a labeled modified deoxyoligonucleotide (dNTP) that can release pyrophosphate to produce fluorescence and has special applications in gene synthesis and sequencing. -
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NCGC00063279
0 ImagesCat. No.: HY-182634CAS No.: 714932-54-4NCGC00063279 is a reversible Werner Syndrome Helicase-Nuclease (WRN) helicase inhibitor with modest selectivity over BLM and FANCJ helicases, and does not inhibit WRN exonuclease activity at active concentrations. NCGC00063279 inhibits Hematopoietic Protein Tyrosine Phosphatase (HePTP) and reduces proliferation of cancer cells. NCGC00063279 can be used for the research of osteosarcoma. -
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HDAC-IN-74
0 ImagesCat. No.: HY-162603CAS No.: 1449310-17-1HDAC-IN-74 (PA) is a dual HDAC/Rribonucleotide reductase(RR) inhibitor, with IC50 values of 10.80 μM and 9.34 μM for HDAC and HDAC, respectively. HDAC-IN-74 can be used in anticancer research. -
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Taq DNA Polymerase, Glycerol-free
0 ImagesCat. No.: HY-E70086ACAS No.: 2304873-37-6Taq DNA Polymerase, Glycerol-free is a thermostable DNA polymerase that can be used in PCR. -
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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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