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| Product | Description | |
|---|---|---|
| UTPαS | UTPαS is an innovatively engineered nucleotide analog emerging as an invaluable instrument, facilitating in-depth investigations into RNA-associated mechanisms. Remarkably versatile, this modified nucleotide analog unleashes a myriad of applications encompassing RNA synthesis, precise labeling techniques along with elucidating ribozymes and unraveling the enigmatic world of RNA-binding proteins. Synonyms: Alpha Thiol UTP; 1-Thio-UTP; Uridine-5'-O-(1-Thiotriphosphate). Grades: ≥ 95 % by HPLC. CAS No. 71214-29-4. Molecular formula: C9H15N2O14P3S (free acid). Mole weight: 500.20 (free acid). |  |
| UTP-γ-AmNS | UTP-γ-AmNS is a highly versatile compound extensively employed in the biomedical sector, serving as a pivotal precursor for nucleic acid synthesis, finding diverse applications in extensive research of viral infections like HIV and hepatitis. UTP-γ-AmNS assumes an indispensable role in facilitating investigations pertaining to nucleotide metabolism and unraveling the intricate mechanisms governing viral replication. Synonyms: Uridine-5'-triphosphate-γ-(sulfo-1-naphthyl)amide, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C19H22N3O17P3S (free acid). Mole weight: 689.37 (free acid). | |
| UTPγS | UTPγS is a nucleotide analog widely used in biomedical research. It serves as a substrate for enzymes involved in RNA synthesis and modification. UTPγS is employed in studies investigating RNA structure, RNA-protein interactions, and ribozyme activities. It finds applications in the exploration of RNA-based therapeutics and drug development targeting infectious diseases. Synonyms: Uridine-5'-(γ-thio)-triphosphate, Sodium salt. Grades: ≥ 85 % by HPLC, contains approx. 10 % UDP, which UTPγS decomposes to at room temperature. CAS No. 79049-97-1. Molecular formula: C9H15N2O14P3S (free acid). Mole weight: 500.20 (free acid). | |
| UTPγS trisodium salt | UTPγS trisodium salt. Group: Biochemicals. Grades: Purified. CAS No. 1266569-94-1. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| UTPγS trisodium salt | UTPγS trisodium salt is a selective P2Y2 and P2Y4 receptor agonist. Synonyms: Uridine-5'-(γ-thio)-triphosphate trisodium salt. CAS No. 1266569-94-1. Molecular formula: C9H12N2Na3O14P3S. Mole weight: 566.15. | |
| UTP-glucose-1-phosphate uridylyltransferase | UTP--glucose-1-phosphate uridylyltransferase is an enzyme found in yeast, plants, and mammals as it is a key player in carbohydrate metabolism. It has been studied significantly in plants as sugar metabolism and production is seen as important for understanding growth from an agricultural standpoint. Recently, human UDP-glucose pyrophosphorylase has been studied and crystallized, revealing a different type of regulation than other organisms previously studied. Its significance is derived from the many uses of UDP-Glucose including galactose usage, glycogen synthesis, glycoprotein synthesis, and glycolipid synthesis. Group: Enzymes. Synonyms: UDP glucose pyrophosphorylase; glucose-1-phosphate uridylyltransferase; UDPG phosphorylase; UDP. Enzyme Commission Number: EC 2.7.7.9. CAS No. 9026-22-6. UDPG pyrophosphorylase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3303; UTP-glucose-1-phosphate uridylyltransferase; EC 2.7.7.9; 9026-22-6; UDP glucose pyrophosphorylase; glucose-1-phosphate uridylyltransferase; UDPG phosphorylase; UDPG pyrophosphorylase; uridine 5'-diphosphoglucose pyrophosphorylase; uridine diphosphoglucose pyrophosphorylase; uridine diphosphate-D-glucose pyrophosphorylase; uridine-diphosphate glucose pyrophosphorylase. Cat No: EXWM-3303. |  |
| UTP-hexose-1-phosphate uridylyltransferase | α-D-Glucose 1-phosphate can also act as acceptor, but more slowly. Group: Enzymes. Synonyms: galactose-1-phosphate uridylyltransferase; galactose 1-phosphate uridylyltransferase; α-D-galactose 1-phosphate uridylyltransferase; galactose 1-phosphate uridyltransferase; UDPgalactose pyrophosphorylase; uridine diphosphate galactose pyrophosphorylase; uridine diphosphogalactose pyrophosphorylase. Enzyme Commission Number: EC 2.7.7.10. CAS No. 9016-11-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3226; UTP-hexose-1-phosphate uridylyltransferase; EC 2.7.7.10; 9016-11-9; galactose-1-phosphate uridylyltransferase; galactose 1-phosphate uridylyltransferase; α-D-galactose 1-phosphate uridylyltransferase; galactose 1-phosphate uridyltransferase; UDPgalactose pyrophosphorylase; uridine diphosphate galactose pyrophosphorylase; uridine diphosphogalactose pyrophosphorylase. Cat No: EXWM-3226. | |
| UTP - lyophilized | UTP - lyophilized is a freeze-dried form of uridine triphosphate (UTP) commonly used in the biomedical industry. UTP serves as a building block for RNA synthesis and modification, playing a vital role in cellular processes such as gene expression and protein synthesis. It is often utilized in research involving RNA labeling, transcription and RNA structural studies. Synonyms: Uridine 5'-triphosphate, Trisodium salt trihydrate. Grades: > 90 % by HPLC. Molecular formula: C9H12N2Na3O15P3* 3H2O. Mole weight: 604.12. | |
| UTP-monosaccharide-1-phosphate uridylyltransferase | Requires Mg2+ or Mn2+ for maximal activity. The reaction can occur in either direction and it has been postulated that MgUTP and Mg-diphosphate are the actual substrates. The enzyme catalyses the formation of UDP-Glc, UDP-Gal, UDP-GlcA, UDP-L-Ara and UDP-Xyl, showing broad substrate specificity towards monosaccharide 1-phosphates. Mannose 1-phosphate, L-Fucose 1-phosphate and glucose 6-phosphate are not substrates and UTP cannot be replaced by other nucleotide triphosphates. Group: Enzymes. Synonyms: UDP-sugar pyrophosphorylase; PsUSP. Enzyme Commission Number: EC 2.7.7.64. UDP-Sugar pyrophosphorylase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3275; UTP-monosaccharide-1-phosphate uridylyltransferase; EC 2.7.7.64; UDP-sugar pyrophosphorylase; PsUSP. Cat No: EXWM-3275. | |
| UTP - solution | | |
| UTP-xylose-1-phosphate uridylyltransferase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). The systematic name of this enzyme class is UTP:alpha-D-xylose-1-phosphate uridylyltransferase. Other names in common use include xylose-1-phosphate uridylyltransferase, uridylyltransferase, xylose 1-phosphate, UDP-xylose pyrophosphorylase, uridine diphosphoxylose pyrophosphorylase, and xylose 1-phosphate uridylyltransferase. This enzyme participates in nucleotide sugars metabolism. Group: Enzymes. Synonyms: xylose-1-phosphate uridylyltransferase; uridylyltransferase, xylose 1-phosphate; UDP-xylose pyrophosphorylase; uridine diphosphoxylose pyrophosphorylase; xylose 1-phosphate uridylyltransferase. Enzyme Commission Number: EC 2.7.7.11. CAS No. 9026-20-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3227; UTP-xylose-1-phosphate uridylyltransferase; EC 2.7.7.11; 9026-20-4; xylose-1-phosphate uridylyltransferase; uridylyltransferase, xylose 1-phosphate; UDP-xylose pyrophosphorylase; uridine diphosphoxylose pyrophosphorylase; xylose 1-phosphate uridylyltransferase. Cat No: EXWM-3227. | |
| 11-UTP (Biotin) (Biotin-X-5-Aminoallyl-uridine-5-triphosphate, Triethylammonium Salt) | Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 60ul. US Biological Life Sciences. | Worldwide |
| 16-UTP (Biotin) (g-[N-(Biotin-6-amino-hexanoyl-6-aminobutanoyl)]-5-(3-aminoallyl)-uridine-5- Triphosphate, Triethylammonium Salt | Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 60ul. US Biological Life Sciences. | Worldwide |
| 18-UTP (Biotin) (g-[N-(Biotin-6-amino-hexanoyl-6-aminohexanoyl)]-5-(3-aminoallyl)-uridine-5- Triphosphate, Triethylammonium Salt) | Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 60ul. US Biological Life Sciences. | Worldwide |
| 2'-/3'-AHC-UTP | 2'-/3'-AHC-UTP is a ligand in affinity chromatography and can be modified with fluorophores and other markers. Synonyms: 2'- / 3'- O- (6- Aminohexylcarbamoyl)uridine- 5'- O- triphosphate, sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C16H29N4O16P3 (free acid). Mole weight: 626.3 (free acid). | |
| 2-Deoxyuridine-5-triphosphoric acid= dutp | Heterocyclic Organic Compound. Alternative Names: 2-Deoxyuridine-5-Triphosphoric Acid;[[[5-(2,4-dioxopyrimidin-1-yl)-3-hydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxyphosphonic acid;Deoxyuridine triphosphate;deoxy-UTP;2-Deoxyuridine 5-triphosphate solution. CAS No. 1173-82-6. Molecular formula: C9H15N2O14P3. Mole weight: 468.141683. Purity: 0.96. IUPACName: [[(2R,3S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate. Density: 2.01g/cm³. Catalog: ACM1173826. |  |
| 2'-O-Methyl-5-methyl-UTP | 2'-O-Methyl-5-methyl-UTP is a sugar-modified nucleoside triphosphate that increases target affinity and nuclease stability, while reducing immune response. Synonyms: 2'-O-Methyl-5-methyluridine-5'-Triphosphate. Grades: ≥90% by AX-HPLC. Molecular formula: C11H19N2O15P3. Mole weight: 512.19. | |
| 2'-O-Methyl-UTP | 2'-O-Methyl-UTP, a chemical compound utilized in RNA transcription and regulation research, is imperative for RNA synthesis and modification. Through experimentation, it has been demonstrated to augment the stability and translation efficiency of mRNA. This product has amplified interest in studying RNA viruses, cancer, and neurological disorders due to its instrumental role in these fields. Synonyms: 2'-O-Methyluridine-5'-Triphosphate; 2'OMe-UTP. Grades: ≥90% by AX-HPLC. Molecular formula: C10H17N2O15P3. Mole weight: 498.2. | |
| 2'OMe-UTP | 2'OMe-UTP, a modified nucleoside triphosphate substrate utilized by RNA polymerase during in vitro transcription, has been recognized for its ability to enhance RNA durability and decrease immunogenicity. This dynamic compound holds potential for the advancement of RNA-based therapeutics and vaccines. Additionally, it has exhibited great efficacy in the study of RNA-protein interactions and RNA structure, delving deeper into the intricate mechanisms of cellular biology. Synonyms: 2'-O-Methyluridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H17N2O15P3 (free acid). Mole weight: 498.17 (free acid). | |
| 2-Thio-UTP | 2-Thio-UTP is a potent and selective agonist of P2Y2 receptor (EC50 = 0.035 μM). Synonyms: Uridine 5'-(tetrahydrogen triphosphate), 2-thio-; 2-Thiouridine 5'-(tetrahydrogen triphosphate); 2-Thiouridine 5'-triphosphate; ((2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate; 2-thioUTP; 1-[5-O- (Hydroxy{[hydroxy (phosphonooxy) phosphoryl]oxy}phosphoryl) -β -D-ribofuranosyl]-2-thioxo-2, 3-dihydro-4 (1H) -pyrimidinone; 2-thio-1-β-D-ribofuranosyl(3H)pyrimidine-2,4-dione 5'-triphosphate. Grades: ≥95%. CAS No. 35763-29-2. Molecular formula: C9H15N2O14P3S. Mole weight: 500.21. | |
| 3'-O-Methyl-UTP | 3'-O-Methyl-UTP, a modified nucleotide for RNA synthesis studies, seamlessly blends into RNA strands as it is integrated by RNA polymerases, thereby scrutinizing transcription initiation and elongation, as well as modifying RNA stability. Moreover, this modified nucleotide broadens the scope of RNA studies to encompass modifications and dysregulation that underline various ailments, such as cancer and neurodegenerative disorders. Synonyms: 3'-O-Methyluridine-5'-Triphosphate. CAS No. 69113-65-1. Molecular formula: C10H17N2O15P3. Mole weight: 498.1. | |
| 3'-(O-Propargyl)-UTP | 3'-(O-Propargyl)-UTP is an indispensable element in the realm of compound, finding extensive application in research investigations centered around RNA modification. This paramount compound assumes a pivotal function in the research and development of groundbreaking pharmaceuticals aiming at RNA-oriented ailments including viral infections and specific categories of cancer. Owing to its exceptional attributes, it empowers accurate labeling and visualization of RNA molecules, thereby fortifying comprehension of their operations and interplaying within animate cells. Synonyms: 3'-(O-Propargyl)-uridine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H17N2O15P3 (free acid). Mole weight: 522.19. | |
| 4-Thio-ethyl-UTP | 4-Thio-ethyl-UTP, a compound extensively utilized in biomedical research, particularly in the field of RNA splicing and editing, is an immensely versatile alternative substrate to UTP, especially when investigating the function of RNA editing enzymes. Its exclusive selectivity for specific RNA sequences further enhances its usefulness, rendering it an essential tool for studying cancer and genetic disorders. Synonyms: 4-Thio-ethyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C11H19N2O14P3S (free acid). Mole weight: 528.26 (free acid). | |
| 4-Thio-i-butyl-UTP | 4-Thio-i-butyl-UTP, a nucleotide analogue utilized in biomedical studies, offers a unique opportunity to investigate RNA structure and function. With a wide range of applications, it plays a critical role in researching RNA-dependent processes in enzymatic assay systems. Moreover, recent studies have unveiled its antiviral properties, indicating its potential as a powerful drug development candidate for targeting specific viral infections. Synonyms: 4-Thio-iso-butyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C13H23N2O14P3S (free acid). Mole weight: 556.31 (free acid). | |
| 4-Thio-i-propyl-UTP | 4-Thio-i-propyl-UTP, a biochemical compound used in biomedical research, is known for its efficacy in the evaluation of P2Y receptor function. Scientists heavily rely on it to look at signaling pathways implicated in diseases affecting multiple organ systems such as cancer, diabetes, and neurodegenerative disorders. This substrate has the power to activate adenylate cyclase through P2Y receptor-mediated processes. Studying these receptors using this compound has been shown to shed light on pathogenic mechanisms. Its use is well-established across the scientific community, both in vitro and in vivo. Synonyms: 4-Thio-iso-propyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H21N2O14P3S (free acid). Mole weight: 542.27 (free acid). | |
| 4-Thio-methyl-UTP | 4-Thio-methyl-UTP is an intricate compound commonly employed in the realm of investigative research and diagnostics. This distinctive altered nucleotide analog effortlessly integrates into RNA throughout transcription, bestowing itself as a paramount instrument for scrutinizing DNA research and development and RNA alterations. Notably, it showcases exceptional utility in delving into the significant role that precise nucleotides play in influencing the intricate facets of RNA's structural composition and functional behavior. Synonyms: 4-Thio-methyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H17N2O14P3S (free acid). Mole weight: 514.23 (free acid). | |
| 4-Thio-n-propyl-UTP | 4-Thio-n-propyl-UTP is a fundamental biosynthetic molecule,finding multifarious applications in examining the intricate dynamics of RNA research and development and modification. Its existence is a profound comprehension of intricate cellular processes concerning gene expression and regulation can be attained. Additionally, owing to its remarkable attributes, 4-Thio-n-propyl-UTP assumes a critical role in unraveling the nuances of RNA metabolism and development. Synonyms: 4-Thio-n-propyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H21N2O14P3S (free acid). Mole weight: 542.29 (free acid). | |
| 4-Thio-UTP | 4-Thio-UTP is an agonist of P2Y2 and P2Y4 receptors that can influence on transcription process to terminate chain extension. Synonyms: 4-Thiouridine-5'-Triphosphate; Thio UTP. Grades: ≥ 95% by HPLC. CAS No. 31556-28-2. Molecular formula: C9H15N2O14P3S (free acid). Mole weight: 500.20 (free acid). | |
| 4-UTP (Biotin) (g-N-(Biotin)-5-(3-aminoallyl)-uridine-5triphosphate, Triethylammonium Salt | Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 60ul. US Biological Life Sciences. | Worldwide |
| 5-(3-Azidopropyl)-UTP 4TEA | 5-(3-Azidopropyl)-UTP 4TEA is used in the synthetic preparation of enzymic incorporation of azide-modified UTP analog into oligoribonucleotides for post transcriptional chemistry functionalization. Synonyms: 5-(3-Azidopropyl)-uridine 5'-(tetrahydrogen triphosphate) Compd. with N,N-diethylethanamine (1:4); 5-(3-Azidopropyl)-uridine 5'-Triphosphate 4TEA. CAS No. 1354419-13-8. Molecular formula: C36H80N9O15P3. Mole weight: 971.99. | |
| 5,6-Dihydro-5-Me-UTP | 5,6-Dihydro-5-Me-UTP is a nucleotide analog that plays a vital role in biomedicine as a potent activator of P2Y receptors. It has demonstrated successful results in the treatment of various diseases such as asthma and inflammatory bowel disease, among others. This compound has also been found to be useful for studying the physiology and pharmacology of P2Y receptors. Synonyms: 5,6-Dihydro-5-Methyluridine-5'-Triphosphate. Grades: ≥90% by AX-HPLC. Molecular formula: C10H19N2O15P3. Mole weight: 500.18. | |
| 5,6-Dihydro-UTP | 5,6-Dihydro-UTP, a nucleotide analog, displays agonist activity at P2Y receptors and serves as a beneficial tool in the study of said receptors in biomedical research. Its multifaceted potential, including implications for the treatment of diseases like cancer and diabetes, make it an exceedingly valuable addition to experimental studies. Synonyms: 5,6-Dihydrouridine-5'-Triphosphate. Grades: ≥90% by AX-HPLC. Molecular formula: C9H17N2O15P3. Mole weight: 486.16. | |
| 5-Azido-C3-UTP | 5-Azido-C3-UTP can be incorporated into RNA by T7 RNA polymerase-mediated in vitro transcription. Synonyms: 5-(3-Azidopropyl)-uridine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N5O15P3 (free acid). Mole weight: 567.23 (free acid). | |
| 5-Azido-PEG4-UTP | 5-Azido-PEG4-UTP, a cutting-edge tool for RNA labeling and detection, is an enzymatic synthesis marvel that effortlessly affords azide-functionalized RNA probes for non-radioactive RNA detection via click chemistry. With its extensive use for RNA target detection in both vitro and in vivo, this product steers the course for scientific breakthroughs in RNA research. Synonyms: 5-Azido-PEG4-uridine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C23H39N6O20P3 (free acid). Mole weight: 812.14 (free acid). | |
| 5-Azido-UTP Triethylamine Salt | 5-Azido-UTP Triethylamine Salt is used in the synthesis of 5-azido UDP glucose which is used as affinity probes for nucleotide diphosphate sugar binding sites. Synonyms: 5-Azido-uridine 5'-(Tetrahydrogen Triphosphate) Triethylamine Salt. Molecular formula: C9H14N5O15P3 x(C6H15N). Mole weight: 525.15. | |
| 5-Bromo-UTP | 5-Bromo-UTP is commonly used to label RNA through being incorporated into RNA for the detection with anti-5-Bromo-UTP antibodies and for the random-mutation introduction. Synonyms: (5Br-UTP); 5-Bromo-uridine-5'-triphosphate, Sodium salt; 5-BrUTP. Grades: ≥ 95% by HPLC. Molecular formula: C9H14N2O15P3Br (free acid). Mole weight: 563.03 (free acid). | |
| 5-Br-UTP | 5-Br-UTP is a base modified ribonucleoside triphosphate used in SELEX technology to provide thermal stability and nuclease resistance to aptamers. Synonyms: 5-Bromouridine-5'-Triphosphate. Grades: ≥90% by AX-HPLC. Molecular formula: C9H14N2O15P3Br. Mole weight: 563.0. | |
| 5-Carboxymethylester-UTP | 5-Carboxymethylester-UTP is a derivative of uridine triphosphate (UTP) which is commonly used in molecular biology research. It can be used together with enzymes to synthesize RNA transcripts with modified 3'-ends without altering the coding sequence. This modification can improve the stability of RNA, making it a useful tool for drug discovery and gene expression studies. Synonyms: 5-Carboxymethylesteruridine-5'-Triphosphate; 5camUTP. Grades: ≥95% by AX-HPLC. Molecular formula: C11H17N2O17P3. Mole weight: 542.1. | |
| 5-Carboxy-UTP | 5-Carboxy-UTP, a nucleotide analog renowned for its versatility and efficacy, is a highly sought-after compound in the realm of biomedicine. Widely employed in the study of RNA processing enzymes and the regulation of RNA metabolism, this exquisite molecule exhibits remarkable potential for the identification of RNA modifications and the creation of diagnostic tools capable of combating notorious afflictions such as cancer and viral infections. Synonyms: 5-Carboxyuridine-5'-Triphosphate; 5-caUTP. Grades: ≥95% by AX-HPLC. Molecular formula: C10H15N2O17P3. Mole weight: 528.1. | |
| 5-DBCO-PEG4-UTP | 5-DBCO-PEG4-UTP is a paramount compound, serving as an indispensable tool for effectuating the covalent bonding of PEGylated substances to RNA, thereby enabling precise drug administration and molecular visualization. Synonyms: 5-Dibenzylcyclooctyl-PEG4-uridine-5'-triphosphate, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C42H54N5O22P3 (free acid). Mole weight: 1073.82 (free acid). | |
| 5-Fluoro-UTP | 5-Fluoro-UTP is an DNA/RNA synthesis inhibitor that terminate synthesis of nucleotide through inhibiting thymidylate synthase. It is used as an anticancer drug. Uses: 5-fluoro-utp is an dna/rna synthesis inhibitor. Synonyms: (5F-UTP); 5-Fluoro-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 3828-96-4. Molecular formula: C9H14N2O15P3F (free acid). Mole weight: 502.13 (free acid). | |
| 5-Formyl-UTP | 5-Formyl-UTP is an indispensable constituent predominantly applied in investigations pertaining to RNA modifications and transcriptional regulation. This invaluable compound contributes to the research of diverse medical conditions, including cancer. By acting as a substrate for RNA labeling and detection, it expedites the exploration of these ailments. Furthermore, its integration into RNA sequences facilitates an enhanced comprehension of RNA metabolism and intricate cellular mechanisms. Synonyms: 5-Formyluridine-5'-Triphosphate; 5-fUTP; 5-FoUTP. Grades: ≥90% by AX-HPLC. Molecular formula: C10H15N2O16P3. Mole weight: 512.15. | |
| 5-hme-UTP | 5-hme-UTP, the cutting-edge solution widely applied in biomedicine to scrutinize RNA, is a remarkable discovery. This chemically modified uridine triphosphate profoundly enriches RNA, rendering it selectively detectable. Expeditions using 5-hme-UTP have evinced its dendritic distribution, unveiling molecular sequences implicated in sundry ailments like cancer and neurodegenerative diseases. Hence, 5-hme-UTP has emerged as a pivotal tool to dissect RNA patterns and unravel the indelible complexities of life. Synonyms: 5-Hydroxymethyluridine-5'-Triphosphate; 5-hm-UTP; 5-Hydroxymethyl-UTP; 5-HmUTP. Grades: ≥95% by AX-HPLC. Molecular formula: C10H17N2O16P3. Mole weight: 514.7. | |
| 5-Hydroxy-UTP | 5-Hydroxy-UTP is an indispensable nucleotide analog, emerging as an alluring vanguard for unveiling the intricate foundations of RNA editing processes. Its resplendent implications extend their tendrils towards an incomparable studying of afflictions such as cancer and neurological disorders. Synonyms: 5-Hydroxyuridine-5'-Triphosphate; 5-hoUTP. Grades: ≥ 95% by HPLC. Molecular formula: C9H15N2O16P3 (free acid). Mole weight: 499.96 (free acid). | |
| 5-Iodo-UTP | 5-Iodo-UTP is a modified nucleotide used to detect RNA expression and to label RNA for hybridization. It is commonly used in biomedical research such as in vitro transcription for the synthesis of labeled RNA and in RNA-protein interaction assays. Synonyms: (5I-UTP); 5-Iodo-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 34198-43-1. Molecular formula: C9H14N2O15P3I (free acid). Mole weight: 610.04 (free acid). | |
| 5-MOM-UTP | 5-MOM-UTP, a nucleotide analog, is utilized in molecular biology research as a tool for exploring RNA processing pathways as well as RNA editing. Moreover, it is employed for investigating neuronal plasticity mechanisms, alongside developing novel drugs for neurological and psychiatric disorders which has been found to be efficacious in addressing epilepsy and schizophrenia. Synonyms: 5-Methoxymethyluridine-5'-Triphosphate; ((2R,3S,4R,5R)-3,4-dihydroxy-5-(5-(methoxymethyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl triphosphate; N1-MOM-Pseudo-UTP; 1-MOM-Pseudo-UTP. Molecular formula: C11H19N2O16P3. Mole weight: 528.2. | |
| 5-Vinyl-UTP | 5-Vinyl-UTP is a vital tool in the biomedical industry used for the research and development of modified RNA molecules. This compound is commonly employed in research to investigate RNA tertiary structures, RNA-protein interactions and RNA enzymatic activities. Furthermore, 5-Vinyl-UTP facilitates the study of RNA-related diseases and the development of potential RNA-based therapeutics for a range of disorders. Grades: ≥ 95% by HPLC. Molecular formula: C11H17N2O15P3 (free acid). Mole weight: 510.18 (free acid). | |
| 6-Aza-UTP | 6-Aza-UTP is a P2Y2 receptor agonist. Synonyms: 6-Azauridine 5'-triphosphoric acid. Grades: ≥90% by AX-HPLC. CAS No. 6198-30-7. Molecular formula: C8H14N3O15P3 (free acid). Mole weight: 485.13 (free acid). | |
| 6-FAM-11-UTP | 6-FAM-11-UTP is a fluorescent nucleotide analog, possessing the ability to be seamlessly integrated into RNA during the transcription process. This unique characteristic facilitates the visual exploration and identification of RNA molecules, empowering researchers to unravel the intricate workings of these vital biomolecules. Its diverse applications encompass a wide range of studies such as transcriptional investigations, RNA labeling endeavors and the real-time tracking of mRNA research and development. Synonyms: 5-[3-(6-(fluoresceinyl-6-carboxamido)hexanoylamido)-propenyl]- uridine-5'-triphosphate, triethylammonium or tetralithium (optional) salt. Grades: ≥ 95%. | |
| AA-UTP | AA-UTP is a substrate for RNA polymerase with amino group that can be labeled with a fluorescent dye, biotin or other markers. Synonyms: 5- (3- Aminoallyl)uridine- 5'- O- triphosphate. Grades: ≥ 95% by HPLC. CAS No. 85280-66-6. Molecular formula: C12H20N3O14P3 (free acid). Mole weight: 539.2 (free acid). | |
| Aminoallyl-UTP - 5/6-TAMRA | Aminoallyl-UTP - 5/6-TAMRA, a fluorescent probe of noteworthy application, has come to the forefront as a key constituent in RNA labeling. With its principal utility being in microarray analysis and in situ hybridization assays, it effectively serves the purpose of identifying gene expression patterns and studying RNA localization. The inclusion of Aminoallyl-UTP - 5/6-TAMRA as a staple tool in research leads to an advanced understanding of RNA-based diseases such as cancer and neurodegenerative disorders. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with 5/6-TAMRA, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C37H40N5O19P3 (free acid). Mole weight: 951.66 (free acid). | |
| Aminoallyl-UTP - 5-FAM | Aminoallyl-UTP - 5-FAM is an invaluable compound, serving as a fundamental instrument for the meticulous labeling of biomolecules. Operating seamlessly within this domain, it provides an avenue for the streamlined research and development of aminoallyl-modified RNA, thus harnessing the potential for conjugation with the renowned fluorescent dye 5-FAM. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with 5 FAM, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C33H30N3O21P3 (free acid). Mole weight: 897.52 (free acid). | |
| Aminoallyl-UTP - 6-FAM | Aminoallyl-UTP - 6-FAM serves as a game-changing tool in molecular biology for the labeling of RNA with fluorescent dyes. Incorporating itself seamlessly into RNA by T7, SP6 or T3 RNA polymerases, it has expansive usage, catering to a niche demand of detecting RNA expression levels in vitro. Gene expression studies, RNA interference research, and drug discovery for assorted diseases including cancers, neurodegenerative disorders, and infectious diseases are areas where Aminoallyl-UTP - 6-FAM shows true prowess. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with 6 FAM, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C33H30N3O21P3 (free acid). Mole weight: 897.52 (free acid). | |
| Aminoallyl-UTP - 6-JOE | Aminoallyl-UTP - 6-JOE is a vital recompound for labeling and detection purposes. By incorporating Aminoallyl group and 6-JOE dye into UTP, this compound enables sensitive nucleic acid labeling, hybridization assay and detection in various applications such as gene expression analysand RNA localization studies. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with 6-JOE, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C35H32Cl2N3O23P3 (free acid). Mole weight: 1025.00 (free acid). | |
| Aminoallyl-UTP - 6-ROX | Aminoallyl-UTP - 6-ROX, a labeled nucleotide serving as a vital tool for RNA labeling and detection, acquires an immense prospect in pre-mRNA splicing, mRNA translation, and RNA transcription. As a quintessential component of biomedical research, it aids in RNA imaging and tracking. Pertinently, it assists in evaluating mRNA expression levels in cells and tissue, impelling its incorporation as an indispensable entity for diagnosing and treating numerous ailments, ranging from cancer to neurological disorders. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with 6-ROX, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C45H48N5O19P3 (free acid). Mole weight: 1055.81 (free acid). | |
| Aminoallyl-UTP - ATTO-390 | Aminoallyl-UTP - ATTO-390, a prominent RNA labeling agent in biomedicine, is multifarious in its applications; gene expression analysis, sequencing, and mRNA detection are just a few. Moreover, this revolutionary compound is gaining recognition in the field of neurodegenerative disease treatment, including cancer and Alzheimer's. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 390, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C32H43N4O18P3 (free acid). Mole weight: 864.63 (free acid). | |
| Aminoallyl-UTP - ATTO-425 | Aminoallyl-UTP is a chemical compound used in biomedical research to label RNA for downstream analysis. It can be incorporated into RNA during transcription and subsequently detected through specific fluorescent markers, such as ATTO-425. The labeled RNA can then be visualized and quantified, making it an invaluable tool in the study of gene expression and regulation. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 425, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C34H45N4O20P3 (free acid). Mole weight: 922.66 (free acid). | |
| Aminoallyl-UTP - ATTO-465 | Aminoallyl-UTP is an indispensable tool, playing a pivotal role in the labeling of RNA molecules for diverse research endeavours. Through its utilization, the proficient research of aminoallyl-UTP labeled RNA becomes attainable, thereby facilitating comprehensive analysis of gene expression, intricate investigations on RNA localization and meticulous detection of mRNA. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 465, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C29H35N6O16P3 (free acid). Mole weight: 816.54 (free acid). | |
| Aminoallyl-UTP - ATTO-488 | Aminoallyl-UTP - ATTO-488 is a fluorescent modified nucleotide used for labeling RNA transcripts during in vitro transcription and subsequent detection by fluorescence microscopy or flow cytometry. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 488, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C37H41N6O24P3S3 (free acid). Mole weight: 1110.08 (free acid). | |
| Aminoallyl-UTP - ATTO-495 | Aminoallyl-UTP - ATTO-495 is a valuable compound enzymatically incorporated into RNA, enabling its specific labeling and subsequent detection. ATTO-495 is a fluorescent dye that can be conjugated to aminoallyl-UTP-labeled RNA for visualization and imaging purposes. This compound is widely used in gene expression analysis, RNA localization studies and RNA sequencing applications in the biomedical industry. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 495, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C33H43N6O16P3 (free acid). Mole weight: 872.65 (free acid). | |
| Aminoallyl-UTP - ATTO-532 | Aminoallyl-UTP - ATTO-532 is a highly versatile and efficient tool utilized in compound for RNA labeling and imaging applications. It acts as a modified nucleotide used in the research and development of labeled RNA probes. Aminoallyl-UTP - ATTO-532 offers excellent fluorescence properties, facilitating precise detection and visualizing RNA sequences for diagnostic purposes and disease research. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 532, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C41H49N6O24P3S2 (free acid). Mole weight: 1166.15 (free acid). | |
| Aminoallyl-UTP - ATTO-540Q | Aminoallyl-UTP is a nucleotide analog commonly used in RNA labeling for microarray analysis, Northern blotting, and in situ hybridization. It can be utilized for the synthesis of aminoallyl-modified RNA probes for the detection and quantification of specific RNA molecules, including those associated with cancer, neurological disorders, and infectious diseases. ATTO-540Q is a fluorescent dye commonly used for labeling RNA molecules generated using aminoallyl-UTP, allowing for sensitive and specific detection of RNA targets. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 540Q, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 540Q (free acid). Mole weight: 1079.22 (free acid). | |
| Aminoallyl-UTP - ATTO-550 | Aminoallyl-UTP - ATTO-550 is an extraordinary fluorescent nucleotide analog with immense potential, unveiling its profound capability for labeling and visualizing RNA molecules. Its radiant ATTO-550 dye reveals an unrivaled aptitude for fluorescence in situ hybridization (FISH) applications, enabling meticulous scrutiny of gene expression intricacies. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 550, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 550 (free acid). Mole weight: 1114.22 (free acid). | |
| Aminoallyl-UTP - ATTO-565 | Aminoallyl-UTP, whose alternative name is ATTO-565, is a type of modified nucleotide often utilized in RNA labeling with the purpose of sensing gene expression and transcriptional activity. It is expertly employed in fluorescence in situ hybridization (FISH) and other comparable techniques. With a broad range of labeling methods available, Aminoallyl-UTP can easily detect specific mRNA sequences. Not to mention, it entices with an elevated signal-to-noise ratio and exceptional labeling efficacy of RNA fragments - both of which are promising attributes for conducting biomedical research. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 565, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C43H48N5O19P3 (free acid). Mole weight: 1031.79 (free acid). | |
| Aminoallyl-UTP - ATTO-580Q | Aminoallyl-UTP - ATTO-580Q is a valuable tool in the biomedical industry used for labeling RNA molecules in various applications, including gene expression analysand mRNA sequencing. This fluorescent dye-conjugated nucleotide allows for specific detection and visualization of RNA aiding in the study and understanding of cellular functions and diseases. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 580Q, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 580Q (free acid). Mole weight: 1215.22 (free acid). | |
| Aminoallyl-UTP - ATTO-590 | Aminoallyl-UTP - ATTO-590 is a fluorescent nucleotide analog used for labeling RNA through enzymatic incorporation during transcription. Aminoallyl-UTP - ATTO-590 is commonly used in fluorescent in situ hybridization (FISH) experiments to detect specific RNA molecules and in microarray gene expression studies. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 590, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H56N5O19P3 (free acid). Mole weight: 1111.92 (free acid). | |
| Aminoallyl-UTP - ATTO-594 | Aminoallyl-UTP-ATTO-594, a modified nucleotide used mainly in biochemistry, enables the labeling of RNA molecules to investigate gene expression. Toxicogenomics has been adopted to discover gene expression patterns where this product proves valuable. Incorporating Aminoallyl-UTP-ATTO-594 into RNA through in vitro transcription allows for easy detection through fluorescence microscopy. The scientific community benefits from this versatile product that aids in the study of various diseases and their associated gene expression patterns. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 594, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 594 (free acid). Mole weight: 1326.22 (free acid). | |
| Aminoallyl-UTP - ATTO-612Q | Aminoallyl-UTP - ATTO-612Q is a vital tool extensively used in the biomedical industry employed to label RNA for various applications including fluorescence in situ hybridization (FISH), real-time PCR and microarray analysis. This compound facilitates the detection and identification of RNA molecules involved in gene expression and contributes to the study of diseases such as cancer, neurodegenerative disorders and viral infections. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 612Q, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 612Q (free acid). Mole weight: 1211.22 (free acid). | |
| Aminoallyl-UTP - ATTO-620 | Aminoallyl-UTP, a derivate of uridine triphosphate, stands as a proficient option for RNA detection assays. When paired with ATTO-620, it presents itself as an invaluable aid in visualizing and quantifying RNA, facilitating a more thorough domain for biomedical research. But alas, its potential doesn't stop there. Its medicinal application in the treatment of severe ailments, such as cancer and viral infections, only magnifies its already impressive nature. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 620, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 620 (free acid). Mole weight: 1032.22 (free acid). | |
| Aminoallyl-UTP - ATTO-633 | Aminoallyl-UTP is an indispensable compound employed for the purpose of labeling and analysis, playing a crucial role in RNA research by serving as a precursor. Through its utilization, the inclusion of aminoallyl groups into RNA molecules is made possible. By virtue of its conjugation with ATTO-633 dye is aminoallyl-UTP contributes to the enhancement of fluorescence detection, thereby facilitating the tracking and examination of RNA molecules. Synonyms: 5-(3-Aminoallyl)-uridine-5'-triphosphate, labeled with ATTO 633, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H20N3O15P3- ATTO 633 (free acid). Mole weight: 1072.22 (free acid). | |
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