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| Product | Description | |
|---|---|---|
| N-Trityl Losartan-d4 | A protected form of labeled Losartan (an antihypertensive). Group: Biochemicals. Alternative Names: 2-Butyl-4-chloro-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl-d4]-4-yl]methyl]-1H-imidazole-5-methanol; Trityllosartan-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| N-Trityl Losartan-d4 Carboxaldehyde | A labeled intermediate in the synthesis of the EXP 3174, a metabolite of Losartan. Group: Biochemicals. Alternative Names: 2-Butyl-4-chloro-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Trityl Losartan Isomer | Intermediate in the preparation of Losartan impurities. Group: Biochemicals. Alternative Names: 2-Butyl-5-chloro-1-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-1H-imidazole-4-methanol. Grades: Highly Purified. CAS No. 133727-10-3. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| N-Trityl-L-proline diethylammonium salt | N-Trityl-L-proline diethylammonium salt. Synonyms: Trt-Pro-OH DEA; (S)-1-Tritylpyrrolidine-2-carboxylic acid diethylammonium salt. CAS No. 80514-78-9. Molecular formula: C28H34N2O2. Mole weight: 430.58. |  |
| N-Trityl Olmesartan-d6 Ethyl Ester | N-Trityl Olmesartan-d6 Ethyl Ester. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Trityl Olmesartan Ethyl Ester | N-Trityl Olmesartan Ethyl Ester. Group: Biochemicals. Alternative Names: 4-(1-Hydroxy-1-methylethyl)-2-propyl-1-[[2'-[2-(triphenylmethyl)-2H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-. Grades: Highly Purified. CAS No. 172875-59-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Trityl Olmesartan Medoxomil Methyl Ether | N-Trityl Olmesartan Medoxomil Methyl Ether is an intermediate in the synthesis of Olmesartan Medoxomil (O550000), an angiotensin II receptor antagonist used as an anti-hypertensive agent. Group: Biochemicals. Alternative Names: (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(2-Methoxypropan-2-yl)-2-propyl-1-((2'-(2-trityl-2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-5-carboxylate. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| N-Trityl Olmesartan Methyl Ketone | N-Trityl Olmesartan Methyl Ketone is an derivative of Olmesartan Medoxomil (O550000). Olmesartan Medoxomil is an angiotensin II receptor antagonist. Used as an anti-hypertensive agent. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Trityl O-Methyl Ether Olmesartan Acid | N-Trityl O-Methyl Ether Olmesartan Acid is an intermediate in the synthesis of Olmesartan Acid (O550001), an angiotensin II receptor antagonist used as an anti-hypertensive agent. Group: Biochemicals. Alternative Names: 4-(2-Methoxypropan-2-yl)-2-propyl-1-((2'-(2-trityl-2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-5-carboxylic Acid. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| N-Trityl O-Methyl Ether Olmesartan Acid Ethyl Ester | N-Trityl O-Methyl Ether Olmesartan Acid Ethyl Ester is an intermediate in the synthesis of Olmesartan Acid (O550001), an angiotensin II receptor antagonist used as an anti-hypertensive agent. Group: Biochemicals. Alternative Names: Ethyl 4-(2-Methoxypropan-2-yl)-2-propyl-1-((2'-(2-trityl-2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-5-carboxylate. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| N-Trityl-trimethylenediamine, polymer bound | Pre-loaded resins for solid phase peptide and organic synthesis. Synonyms: 1,3-Diaminopropane trityl resin; N-(3-Aminopropyl)tritylamine, polymer bound. | |
| N-Trityl-trimethylenediamine, polymer bound | N-Trityl-trimethylenediamine, polymer bound. Group: Biochemicals. Alternative Names: 1,3-Diaminopropane trityl resin; N- (3-Aminopropyl) tritylamine, polymer bound. Grades: Highly Purified. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| N-Trityl-trimethylenediamine, polymer bound, 0.3-0.8 meq/g (substitution) | N-Trityl-trimethylenediamine, polymer bound, 0.3-0.8 meq/g (substitution). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| N type Bismuth(III) telluride | N type Bismuth(III) telluride. Group: Semiconductor blocks. CAS No. 1304-82-1. |  |
| nTZDpa | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| nTZDpa | nTZDpa. Group: Biochemicals. Grades: Purified. CAS No. 118414-59-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NU 1025 | NU 1025. Group: Biochemicals. Grades: Purified. CAS No. 90417-38-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NU-1025 | ?97% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| NU2058 | >98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| NU 2058 | NU 2058. Group: Biochemicals. Grades: Purified. CAS No. 161058-83-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NU6027 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| NU6102 | NU6102 is a potent CDK1 and CDK2 inhibitor with IC50s of 9.5 nM and 5.4 nM for CDK1/cyclinB and CDK2/cyclinA3, respectively. NU6102 shows selectivity for CDK1/CDK2 over CDK4 (IC50 of 1.6 ?M), DYRK1A (IC50 of 0.9 ?M), PDK1 (IC50 of 0.8 ?M) and ROCKII (IC50 of 0.6 ?M)[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 444722-95-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15569. |  |
| NU6102 (O6-Cyclohexylmethyl-2- (4-sulfamoylanilino) purine) | Potent CDK1/cyclin B (IC50 = 9.5nM) and CDK2/cyclin A3 (IC50 = 5.4nM) inhibitor. 1,000-fold more potent than NU2058. Selective for CDK1 and CDK2 compared to CDK4/D1 (IC50 = 1.6uM), DYRK1A (IC50 = 0.9uM), PDK1 (IC50 = 0.8uM) and ROCKII (IC50 = 0.6uM). Inhibits cell growth. Group: Biochemicals. Alternative Names: O6-Cyclohexylmethyl-2- (4-sulfamoylanilino) purine. Grades: Highly Purified. CAS No. 444722-95-6. Pack Sizes: 1mg, 5mg. Molecular Formula: C18H22N6O3S, Molecular Weight: 402.5. US Biological Life Sciences. | Worldwide |
| NU6140 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| NU 6140 | NU 6140. Group: Biochemicals. Grades: Purified. CAS No. 444723-13-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NU7026 | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| NU 7026 | NU 7026. Group: Biochemicals. Grades: Purified. CAS No. 154447-35-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NU 7026 | NU 7026 (LY293646) is a novel specific DNA-PK inhibitor with IC50 of 0.23 ?M, also inhibits PI3K with IC50 of 13 ?M. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LY293646. CAS No. 154447-35-5. Pack Sizes: 5 mg; 10 mg; 50 mg. Product ID: HY-15719. | |
| NU 7441 | A potent novel DNA-dependent protein kinase inhibitor models of human cancer. Antitumor agent. Group: Biochemicals. Alternative Names: 8-(4-Dibenzothienyl)-2-(4-morpholinyl)-4H-1-benzopyran-4-one; KU 57788. Grades: Highly Purified. CAS No. 503468-95-9. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C??H??NO?S, Molecular Weight: 413.49. US Biological Life Sciences. | Worldwide |
| NU9056 | NU9056 is a potent and selective Tip60 (KAT5) histone acetyltransferase inhibitor with an [1][2] of 2 μM. NU9056 shows >16-fold selectivity for Tip60 over PCAF, p300 and GCN5. NU9056 induces apoptosis of prostate cancer cells[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1450644-28-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-110127. | |
| NU 9056 | NU 9056. Group: Biochemicals. Grades: Purified. CAS No. 1450644-28-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| NUAK1, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| NUAK2, active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| NUAK family SNF1-like kinase 2 (446-455) | NUAK family SNF1-like kinase 2 (446-455) is a peptide derived from NUAK family SNF1-like kinase 2. NUAK family SNF1-like kinase 2 induces cell-cell detachment by increasing F-actin conversion to G-actin. Synonyms: Omphalocele kinase 2 (446-455). | |
| nuatigenin 3β-glucosyltransferase | Some other sapogenins can act as glucosyl acceptors. Involved in the biosynthesis of plant saponins. Not identical with EC 2.4.1.173 (sterol 3β-glucosyltransferase) or EC 2.4.1.193 (sarsapogenin 3β-glucosyltransferase). Group: Enzymes. Synonyms: uridine diphosphoglucose-nuatigenin glucosyltransferase. Enzyme Commission Number: EC 2.4.1.192. CAS No. 108891-57-2. 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-2419; nuatigenin 3β-glucosyltransferase; EC 2.4.1.192; 108891-57-2; uridine diphosphoglucose-nuatigenin glucosyltransferase. Cat No: EXWM-2419. |  |
| NUC-7738 | NUC-7738, an aryloxy phosphoramidate of 3-Deoxyadenosine, is a 5-aryloxy phosphoramidate prodrug of 3-Deoxyadenosine (3-dA). NUC-7738 has potent cytotoxic activity against a panel of hematological cancer cell lines. NUC-7738 can be used in research of cancer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2348493-39-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-136506. | |
| Nuchensin | Nuchensin is a natural product found in Lantana montevidensis. Synonyms: 5,6,3'-Trihydroxy-7,4'-dimethoxyflavone; 3',5,6-Trihydroxy-4',7-dimethoxyflavone. Grade: 98%. CAS No. 25782-24-5. Molecular formula: C17H14O7. Mole weight: 330.29. | |
| Nuciferin | Nuciferine is a natural alkaloid compound isolated from the plants Nymphaea caerulea and Nelumbo nucifera. Nuciferine has a profile of action associated with dopamine receptor blockade. Alternative Names: Nuciferin. Sanjoinine E. l-Nuciferine. CAS No. 475-83-2. Product ID: PIPE-0708. Molecular formula: C19H21NO2. Mole weight: 295.4. EINECS: 842-235-9. SMILES: CN1CCC2=CC(=C(C3=C2[C@H]1CC4=CC=CC=C43)OC)OC. Appearance: Powder. Category: Natural Extract. |  |
| Nuciferine | Nuciferine is an antagonist at 5-HT 2A ( IC 50 =478 nM), 5-HT 2C ( IC 50 =131 nM), and 5-HT 2B ( IC 50 =1 μM), an inverse agonist at 5-HT 7 ( IC 50 =150 nM), a partial agonist at D 2 ( EC 50 =64 nM), D 5 ( EC 50 =2.6 μM) and 5-HT 6 ( EC 50 =700 nM), an agonist at 5-HT 1A ( EC 50 =3.2 μM) and D 4 ( EC 50 =2 μM) receptor. Uses: Scientific research. Group: Natural products. CAS No. 475-83-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-N0049. | |
| Nuciferine | Nuciferine is a natural alkaloid compound isolated from the plants Nymphaea caerulea and Nelumbo nucifera. Nuciferine has a profile of action associated with dopamine receptor blockade. Synonyms: Nuciferin; Sanjoinine E; l-Nuciferine. Grade: >98%. CAS No. 475-83-2. Molecular formula: C19H21NO2. Mole weight: 295.375. | |
| Nuciferine | Nuciferine. Group: Biochemicals. Alternative Names: Sanjoinine E. Grades: Plant Grade. CAS No. 475-83-2. Pack Sizes: 20mg. Molecular Formula: C19H21NO2, Molecular Weight: 295.375999999999. US Biological Life Sciences. | Worldwide |
| Nuclear Fast Red | Nuclear Fast Red, an anthraquinone dye, is commonly used in conjunction with an excess of aluminum ions as a red nuclear counterstain. Nuclear fast red has been used as a histochemical and colorimetric reagent for calcium [1]. Nuclear fast red as highly sensitive "off/on" fluorescent probe for detecting guanine [2]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Kernechtrot. CAS No. 6409-77-4. Pack Sizes: 250 mg; 500 mg; 1 g; 5 g. Product ID: HY-D0943. | |
| Nuclear Fast Red (C.I. 60760) | 5g Pack Size. Group: Stains & Indicators. Formula: C14H8NNaO7S. CAS No. 6409-77-4. Prepack ID 35954436-5g. Molecular Weight 357.27. See USA prepack pricing. |  |
| Nuclear Fast Red solution | Nuclear Fast Red solution. Group: Biochemicals. Grades: Highly Purified. CAS No. 6409-77-4. Pack Sizes: 100g, 250g. Molecular Formula: C14H9NO7S·Na. US Biological Life Sciences. | Worldwide |
| nuclear-inclusion-a endopeptidase | The potyviruses cause diseases in plants, and inclusion bodies appear in the host cell nuclei; protein a of the inclusion bodies is the endopeptidase. The enzyme finds practical use when encoded in vectors for the artificial expression of recombinant fusion proteins, since it can confer on them the capacity for autolytic cleavage. It is also reported that transgenic plants expressing the enzyme are resistant to viral infection. Type example of peptidase family C4. Group: Enzymes. Synonyms: potyvirus NIa protease. Enzyme Commission Number: EC 3.4.22.44. CAS No. 139946-51-3. 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-4219; nuclear-inclusion-a endopeptidase; EC 3.4.22.44; 139946-51-3; potyvirus NIa protease. Cat No: EXWM-4219. | |
| Nuclear Localiation Signal Peptide | It is a commonly used nuclear localization signal (NLS) peptide. Synonyms: H-Pro-Lys-Lys-Lys-Arg-Lys-Val-OH; L-prolyl-L-lysyl-L-lysyl-L-lysyl-L-arginyl-L-lysyl-L-valine; NLS (PKKKRKV). Grade: >98%. Molecular formula: C40H78N14O8. Mole weight: 883.14. | |
| Nuclear pore complex protein Nup98 (315-360) | Nuclear pore complex protein Nup98 (315-360) is the 315-360 fragment of the nuclear pore complex (NPC) protein. Synonyms: Ac-Met-Gly-Leu-Phe-Gly-Val-Thr-Gln-Ala-Ser-Gln-Pro-Gly-Gly-Leu-Phe-Gly-Thr-Ala-Thr-Asn-Thr-Ser-Thr-Gly-Thr-Ala-Phe-Gly-Thr-Gly-Thr-Gly-Leu-Phe-Gly-Gln-Thr-Asn-Thr-Gly-Phe-Gly-Ala-Val. Grade: >98%. Molecular formula: C190H288N50O64S. Mole weight: 4328.68. | |
| Nuclear Receptor Inhibitors Library | A unique collection of 420 nuclear receptor signaling targeted compounds for high throughput and high content screening; - Bioactivity and safety confirmed by pre-clinical research and clinical trials; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L1510. Categories: Nuclear Receptor Inhibitors Libraries. |  |
| Nuclear transcription factor Y subunit gamma (275-282) | Nuclear transcription factor Y subunit gamma (275-282) is a 8-aa peptide. Nuclear transcription factor Y subunit gamma is a component of the sequence-specific heterotrimeric transcription factor (NF-Y) which specifically recognizes a 5'-CCAAT-3' box motif found in the promoters of its target genes. Synonyms: CAAT box DNA-binding protein subunit C (275-282); Nuclear transcription factor Y subunit C (275-282). | |
| Nuclear transcription factor Y subunit gamma (28-37) | Nuclear transcription factor Y subunit gamma (28-37) is a 10-aa peptide. Nuclear transcription factor Y subunit gamma is a component of the sequence-specific heterotrimeric transcription factor (NF-Y) which specifically recognizes a 5'-CCAAT-3' box motif found in the promoters of its target genes. Synonyms: CAAT box DNA-binding protein subunit C (28-37); Nuclear transcription factor Y subunit C (28-37). | |
| Nuclear Transport Factor 2?Agarose | saline suspension. Group: Fluorescence/luminescence spectroscopy. | |
| Nuclease-free Water | Nuclease-free Water. Ddh2o is purified by reverse osmosis method. it is suitable for most molecular and cell biology applications. Group: Cloning Enzymes. Purity: 25ml. Storage: Store at Room Temperature. Cat No: CE-3009. | |
| Nuclease P1 | Nuclease P1 is a single-stranded specific endonuclease, it hydrolyzes nucleic acids into 5'-mononucleotides and cleaves the single-stranded region of a double-stranded nucleic acid. Nuclease P1 is one of the most well-known single stranded specific nucleases in the field of molecular biology, it is widely used in the pharmaceutical and food industries [1]. Nuclease P1 can be obtained by fermentation of Penicillium citrinum: through extraction process, ultrafiltration concentration, drying and purification, etc. Uses: Scientific research. Group: Signaling pathways. CAS No. 54576-84-0. Pack Sizes: 250 U. Product ID: HY-P2963. | |
| Nuclease, restrictionendodeoxyribo-, SpeI | Nuclease, restrictionendodeoxyribo-, SpeI. Uses: Designed for use in research and industrial production. Additional or Alternative Names: RESTRICTION ENDONUCLEASES SPE I;SPE I;SPE I RESTRICTION ENZYME;RESTRICTION ENDONUCLEASE SPE I FROM*SPHA EROTILUS SP;spei5'.actagt.3'isolatedfromsphaerotilusspecies;spe i from sphaerotilus sp.;RESTRICTION ENDONUCLEASE SPE I. Product Category: Heterocyclic Organic Compound. CAS No. 115926-60-8. Molecular formula: ClH. Mole weight: 36.46094;g/mol. Purity: 0.96. IUPACName: chlorane. Canonical SMILES: Cl. ECNumber: 231-595-7. Product ID: ACM115926608. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Nuclease, restrictionendodeoxyribo-, StyI | Nuclease, restrictionendodeoxyribo-, StyI. Uses: Designed for use in research and industrial production. Additional or Alternative Names: STY I;STY I RESTRICTION ENZYME;RESTRICTION ENDONUCLEASES STY I;RESTRICTION ENDONUCLEASE STY I FROM ESCH;sty i from escherichia coli strain carrying pst27;RESTRICTION ENDONUCLEASE STY I. Product Category: Heterocyclic Organic Compound. CAS No. 96880-98-7. Purity: 0.96. Product ID: ACM96880987. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nuclease S1, Aspergillus oryzae | Nuclease S1, Aspergillus oryzae is a specific endonuclease that degrades single stranded DNA (ssDNA) and RNA. Nuclease S1 can also remove protruding single-strand ends from double-stranded DNA [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 37288-25-8. Pack Sizes: 10 KU. Product ID: HY-P2773. | |
| Nuclease, Serratia marcescens | Serratia marcescens nuclease (EC 3.1.30.2) is a nonspecific nuclease. Serratia marcescens nuclease has broad utility due to its potent digestive activity toward both DNA and RNA [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Serratia marcescens nuclease. CAS No. 9025-65-4. Pack Sizes: 5 KU; 10 KU; 25 KU. Product ID: HY-131160. | |
| Nucleating Agent ZC-3 | DryPowder. Group: Polymers. CAS No. 135861-56-2. Product ID: (1R)-1-[(4R,4aR,8aS)-2,6-bis(3,4-dimethylphenyl)-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol. Molecular formula: 414.5g/mol. Mole weight: C24H30O6. CC1=C (C=C (C=C1)C2OCC3C (O2)C (OC (O3)C4=CC (=C (C=C4)C)C)C (CO)O)C. InChI=1S/C24H30O6/c1-13-5-7-17 (9-15 (13)3)23-27-12-20-22 (30-23)21 (19 (26)11-25)29-24 (28-20)18-8-6-14 (2)16 (4)10-18/h5-10, 19-26H, 11-12H2, 1-4H3/t19-, 20+, 21-, 22-, 23?, 24?/m1/s1. YWEWWNPYDDHZDI-JJKKTNRVSA-N. | |
| Nucleocidin | Nucleocidin is originally isolated from Str. calvus T 3018 and it is mainly resistant to bacteria, mycoplasma and protozoa. Synonyms: 4'-Fluoro-5'-O-sulfamoyladenosine; Antibiotic T-3018; 4'-C-Fluoroadenosine 5'-sulfamate; NSC 521007. Grade: >98%. CAS No. 24751-69-7. Molecular formula: C10H13FN6O6S. Mole weight: 364.31. | |
| nucleoplasmin ATPase | An acidic nuclear protein that is active in the ATP-dependent assembly of nucleosome cores, in decondensation of sperm chromatin and in other histone-involving processes. Group: Enzymes. Enzyme Commission Number: EC 3.6.4.11. 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-4701; nucleoplasmin ATPase; EC 3.6.4.11. Cat No: EXWM-4701. | |
| Nucleoprotein 118-126 | It is a 9-aa peptide, a fragment of Nucleoprotein. Synonyms: NP (118-126); H-Arg-Pro-Gln-Ala-Ser-Gly-Val-Tyr-Met-OH; L-arginyl-L-prolyl-L-glutaminyl-L-alanyl-L-seryl-glycyl-L-valyl-L-tyrosyl-L-methionine. Grade: ≥95%. CAS No. 124454-83-7. Molecular formula: C43H69N13O13S. Mole weight: 1008.15. | |
| Nucleoprotein (265-273) | Nucleoprotein (265-273) is amino acids 265 to 273 fragment of Nucleoprotein. The highly conserved internal nucleoprotein (NP) is a promising antigen to develop a universal influenza A virus vaccine. Molecular formula: C43H77N15O11. Mole weight: 980.17. | |
| Nucleoprotein (396-404) | Nucleoprotein (396-404) is the 396 to 404 fragment of lymphocytic choriomeningitis virus (LCMV). Nucleoprotein (396-404) is the H-2D(b)-restricted immunodominant epitope and can be used as a molecular model of viral antigen [1] [2]. Uses: Scientific research. Group: Peptides. Alternative Names: NP 396. CAS No. 158475-79-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1571. | |
| Nucleoprotein 396-404 | Nucleoprotein (396-404) is the 396 to 404 fragment of lymphocytic choriomeningitis virus (LCMV). Synonyms: NP 396. Grade: >98%. CAS No. 158475-79-7. Molecular formula: C50H71N13O14. Mole weight: 1078.18. | |
| nucleoside deoxyribosyltransferase | Base1 and base2 represent various purines and pyrimidines. Group: Enzymes. Synonyms: purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyl transferase; deoxyribose transferase; nucleoside trans-N-deoxyribosylase; trans-deoxyribosylase; trans-N-deoxyribosylase; trans-N-glycosidase; nucleoside deoxyribosyltransferase I (purine nucleoside:purine deoxyribosyltransferase: strictly specific for transfer between purine bases); nucleoside deoxyribosyltransferase II [purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyltransferase]. Enzyme Commission Number: EC 2.4.2.6. CAS No. 9026-86-2. NDT. 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-2689; nucleoside deoxyribosyltransferase; EC 2.4.2.6; 9026-86-2; purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyl transferase; deoxyribose transferase; nucleoside trans-N-deoxyribosylase; trans-deoxyribosylase; trans-N-deoxyribosylase; trans-N-glycosidase; nucleoside deoxyribosyltransferase I (purine nucleoside:purine deoxyribosyltransferase: strictly specific for transfer between purine bases); nucleoside deoxyribosyltransferase II [purine(pyrimidine) nucleoside:purine(pyrimidine) deoxyribosyltransferase]. Cat No: EXWM-2689. | |
| Nucleoside Deoxyribosyltransferase II from Lactobacillus leichmanii, Recombinant | Class II N-Deoxyribosyltranferases, DRTases, catalyze the transfer of a 2'-deoxyribosyl group between purines or pyrimidines. In the absence of an acceptor nucleobase, these enzymes display hydrolase activity, converting the nucleoside to its base and a deoxyribose. In lactobacilli species, Nucleoside Deoxyribosyltransferase enzymes are part of the nucleoside salvage pathway for DNA synthesis. Applications: Nucleoside deoxyribosyltransferase ii has been used in a study that assessed its enzymatic synthesis with 2?-deoxyguanosine. nucleoside deoxyribosyltransferase ii has also been used in studies to investigate its molecular cloning, expression and spe. 2.4.2.6. CAS No. 9026-86-2. NDT. Storage: -20°C. Form: lyophilized powder. Source: E. coli. Species: Lactobacillus leichmanii. EC 2.4.2.6; purine (pyrimidine) nucleoside:purine (pyrimidine) deoxyribosyl transferase; deoxyribose transferase; nucleoside trans-N-deoxyribosylase; trans-deoxyribosylase; trans-N-deoxyribosylase; trans-N-glycosidase; nucleoside deoxyribosyltransferase I (purine nucleoside:purine deoxyribosyltransferase:strictly specific for transfer between purine bases); nucleoside deoxyribosyltransferase II [purine (pyrimidine) nucleoside:purine (pyrimidine) deoxyribosyltransferase]; DRTase; Deoxyribose transferase; NDT. Cat No: NATE-0478. | |
| nucleoside-diphosphate kinase | Many nucleoside diphosphates can act as acceptors, while many ribo- and deoxyribonucleoside triphosphates can act as donors. Group: Enzymes. Synonyms: nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. 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-3216; nucleoside-diphosphate kinase; EC 2.7.4.6; 9026-51-1; nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Cat No: EXWM-3216. | |
| Nucleoside-Diphosphate Kinase (Crude Enzyme) | Nucleoside-diphosphate kinases (NDPKs, also NDP Kinase, (poly)nucleotide kinases and nucleoside diphosphokinases) are enzymesthat catalyze the exchange of terminal phosphate between different nucleoside diphosphates (NDP) and triphosphates (NTP) in a reversible manner to produce nucleotide triphosphates. Many NDP serve as acceptor while NTP are donors of phosphate group. The general reaction via ping-pong mechanism is as follows: XDP + YTP ?? XTP + YDP (X and Y each represent different nitrogenous base). NDPK activities maintain an equilibrium between the concentrations of different nucleoside triphosphates such as, for example, when guanosine triphosphate (GTP) produce. activity was briefly purified from engineered E. coli. Applications: Medicine. Group: Enzymes. Synonyms: nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Enzyme Commission Number: EC 2.7.4.6. CAS No. 9026-51-1. NDPK. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. nucleoside 5'-diphosphate kinase; nucleoside diphosphate (UDP) kinase; nucleoside diphosphokinase; nucleotide phosphate kinase; UDP kinase; uridine diphosphate kinase. Pack: 100ml. Cat No: NATE-1829. | |
| nucleoside diphosphate phosphatase | The enzyme, which appears to be limited to metazoa, acts on multiple nucleoside diphosphates as well as on D-ribose 5-diphosphate. Specificity depends on species and isoform. Group: Enzymes. Synonyms: nucleoside-diphosphatase; thiaminpyrophosphatase; UDPase; inosine diphosphatase; adenosine diphosphatase; IDPase; ADPase; adenosinepyrophosphatase; guanosine diphosphatase; guanosine 5'-diphosphatase; inosine 5'-diphosphatase; uridine diphosphatase; uridine 5'-diphosphatase; type B nucleoside diphosphatase; GDPase; CDPase; nucleoside 5'-diphosphatase; type L nucleoside diphosphatase; NDPase; nucleoside diphosphate phosphohydrolase. Enzyme Commission Number: EC 3.6.1.6. CAS No. 9027-69-4. 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-4632; nucleoside diphosphate phosphatase; EC 3.6.1.6; 9027-69-4; nucleoside-diphosphatase; thiaminpyrophosphatase; UDPase; inosine diphosphatase; adenosine diphosphatase; IDPase; ADPase; adenosinepyrophosphatase; guanosine diphosphatase; guanosine 5'-diphosphatase; inosine 5'-diphosphatase; uridine diphosphatase; uridine 5'-diphosphatase; type B nucleoside diphosphatase; GDPase; CDPase; nucleoside 5'-diphosphatase; type L nucleoside diphosphatase; NDPase; nucleoside diphosphate phosphohydrolase. Cat No: EXWM-4632. | |
| nucleoside oxidase | Other purine and pyrimidine nucleosides (as well as 2'-deoxyribonucleosides) are substrates, but ribose and nucleotides are not substrates. The overall reaction takes place in two separate steps, with the 5'-dehydro nucleoside being released from the enzyme to serve as substrate for the second reaction. This enzyme differs from EC 1.1.3.39, nucleoside oxidase (H2O2-forming), as it produces water rather than hydrogen peroxide. Group: Enzymes. Enzyme Commission Number: EC 1.1.3.28. CAS No. 82599-71-1. 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-0406; nucleoside oxidase; EC 1.1.3.28; 82599-71-1. Cat No: EXWM-0406. | |
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