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A unique collection of 255 nucleoside and nucleotide analogues, can be used for research and development of anti-viral, anti-tumor, anti-fungal, and anti-depressive drugs; - Some compounds are in the clinical trial phases or market therapeutic drugs?- Detailed compound information with structure, target, and biological activity description?- NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L1720. Categories: Nucleotide Compounds Libraries.
nucleotide diphosphatase
The enzyme preferentially hydrolyses ATP, but can also hydrolyse other nucleoside 5' triphosphates such as GTP, CTP, TTP and UTP to their corresponding monophosphates. In vitro the enzyme also acts as a nucleotidohydrolase on ADP, NAD+, NADP+, FAD, and CoA. Group: Enzymes. Synonyms: ENPP1 (gene name); nucleotide pyrophosphatase; nucleotide-sugar pyrophosphatase; nucleoside-triphosphate diphosphatase. Enzyme Commission Number: EC 3.6.1.9. CAS No. 9032-64-8. Nucleotide Pyrophosphatase. 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-4643; nucleotide diphosphatase; EC 3.6.1.9; 9032-64-8; ENPP1 (gene name); nucleotide pyrophosphatase; nucleotide-sugar pyrophosphatase; nucleoside-triphosphate diphosphatase. Cat No: EXWM-4643.
nucleotide diphosphokinase
The enzyme acts on the 5'-mono-, di- and triphosphate derivatives of purine nucleosides. Group: Enzymes. Synonyms: nucleotide pyrophosphokinase; ATP:nucleotide pyrophosphotransferase; ATP nucleotide 3'-pyrophosphokinase; nucleotide 3'-pyrophosphokinase. Enzyme Commission Number: EC 2.7.6.4. CAS No. 53167-92-3. 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-3223; nucleotide diphosphokinase; EC 2.7.6.4; 53167-92-3; nucleotide pyrophosphokinase; ATP:nucleotide pyrophosphotransferase; ATP nucleotide 3'-pyrophosphokinase; nucleotide 3'-pyrophosphokinase. Cat No: EXWM-3223.
2',3'-cyclic-nucleotide 2'-phosphodiesterase
Also hydrolyses 3'-nucleoside monophosphates and bis-4-nitrophenyl phosphate, but not 3'-deoxynucleotides. Similar reactions are carried out by EC 3.1.27.3 (ribonuclease T1) and EC 3.1.27.5 (pancreatic ribonuclease). Group: Enzymes. Synonyms: ribonucleoside 2',3'-cyclic phosphate diesterase; 2',3 -cyclic AMP phosphodiesterase; 2',3'-cyclic nucleotidase; cyclic 2',3'-nucleotide 2'-phosphodiesterase; cyclic 2',3'-nucleotide phosphodiesterase; 2',3'-cyclic nucleoside monophosphate phosphodiesterase; 2',3'-cyclic AMP 2'-phosphohydrolase; cyclic phosphodiesterase:3'-nucleotidase; 2',3'-cyclic n. Enzyme Commission Number: EC 3.1.4.16. CAS No. 9037-18-7. 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-3715; 2',3'-cyclic-nucleotide 2'-phosphodiesterase; EC 3.1.4.16; 9037-18-7; ribonucleoside 2',3'-cyclic phosphate diesterase; 2',3 -cyclic AMP phosphodiesterase; 2',3'-cyclic nucleotidase; cyclic 2',3'-nucleotide 2'-phosphodiesterase; cyclic 2',3'-nucleotide phosphodiesterase; 2',3'-cyclic nucleoside monophosphate phosphodiesterase; 2',3'-cyclic AMP 2'-phosphohydrolase; cyclic phosphodiesterase:3'-nucleotidase; 2',3'-cyclic nucleotide phosphohydrolase; 2':3'-cyclic phosphodiesterase; 2':3'-cyclic nucleotide phosphodiesterase:3'-nucleotidase. Cat No: EXWM-3715.
2',3'-cyclic-nucleotide 3'-phosphodiesterase
The brain enzyme acts on 2',3'-cyclic AMP more rapidly than on the UMP or CMP derivatives. An enzyme from liver acts on 2',3'-cyclic CMP more rapidly than on the purine derivatives; it also hydrolyses the corresponding 3',5'-cyclic phosphates, but more slowly. This latter enzyme has been called cyclic-CMP phosphodiesterase. Group: Enzymes. Synonyms: cyclic-CMP phosphodiesterase; 2',3'-cyclic AMP phosphodiesterase; cyclic 2',3'-nucleotide 3'-phosphodiesterase; cyclic 2',3'-nucleotide phosphodiesterase; 2',3'-cyclic nucleoside monophosphate phosphodiesterase; 2',3'-cyclic nucleotide 3'-phosphohydrolase; CNPase; 2',3'-cyclic nucleotide phosphohydrolase; 2':3'-cyclic nucleotide 3'-phosphod. Enzyme Commission Number: EC 3.1.4.37. CAS No. 60098-35-3. 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-3720; 2',3'-cyclic-nucleotide 3'-phosphodiesterase; EC 3.1.4.37; 60098-35-3; cyclic-CMP phosphodiesterase; 2',3'-cyclic AMP phosphodiesterase; cyclic 2',3'-nucleotide 3'-phosphodiesterase; cyclic 2',3'-nucleotide phosphodiesterase; 2',3'-cyclic nucleoside monophosphate phosphodiesterase; 2',3'-cyclic nucleotide 3'-phosphohydrolase; CNPase; 2',3'-cyclic nucleotide phosphohydrolase; 2':3'-cyclic nucleotide 3'-phosphodiesterase; 2':3'-CNMP-3'-ase. Cat No: EXWM-3720.
3',5'-cyclic-nucleotide phosphodiesterase
Acts on 3',5'-cyclic AMP, 3',5'-cyclic dAMP, 3',5'-cyclic IMP, 3',5'-cyclic GMP and 3',5'-cyclic CMP. Group: Enzymes. Synonyms: cyclic 3',5'-mononucleotide phosphodiesterase; PDE; cyclic 3',5'-nucleotide phosphodiesterase; cyclic 3',5'-phosphodiesterase; 3',5'-nucleotide phosphodiesterase; 3':5'-cyclic nucleotide 5'-nucleotidohydrolase; 3',5'-cyclonucleotide phosphodiesterase; cyclic nucleotide phosphodiesterase; 3', 5'-cyclic nucleoside monophosphate p. Enzyme Commission Number: EC 3.1.4.17. CAS No. 9040-59-9. PDE. 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-3716; 3',5'-cyclic-nucleotide phosphodiesterase; EC 3.1.4.17; 9040-59-9; cyclic 3',5'-mononucleotide phosphodiesterase; PDE; cyclic 3',5'-nucleotide phosphodiesterase; cyclic 3',5'-phosphodiesterase; 3',5'-nucleotide phosphodiesterase; 3':5'-cyclic nucleotide 5'-nucleotidohydrolase; 3',5'-cyclonucleotide phosphodiesterase; cyclic nucleotide phosphodiesterase; 3', 5'-cyclic nucleoside monophosphate phosphodiesterase; 3': 5'-monophosphate phosphodiesterase (cyclic CMP); cytidine 3':5'-monophosphate phosphodiesterase (cyclic CMP); cyclic 3',5-nucleotide monophosphate phosphodiesterase; nucleoside 3',5'-cyclic phosphate diesterase; nucleoside-3',5-monophosphate phosphodiesterase. Cat No: EXWM-3716.
a-Nicotinamide adenine dinucleotide phosphate
a-Nicotinamide adenine dinucleotide phosphate, commonly known as NADP+, stands as an indispensable coenzyme within the biomedical industry. Primarily responsible for driving cellular energy production and overseeing redox reactions, it assumes a vital role in numerous disease treatment modalities. Synonyms: a-NADP; a-Triphosphopyridine nucleotide; a-TPN; a-Nicotinamide adenine dinucleotide phosphate; sodium [[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-oxidophosphoryl][(2R,3S,4R,5S)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate. Grades: 95%. CAS No. 108392-03-6. Molecular formula: C21H27N7NaO17P3. Mole weight: 765.39.
a-Nicotinamide mononucleotide
a-Nicotinamide mononucleotide is a pivotal intermediate in the bioresearch of nicotinamide adenine dinucleotide (NAD+), finding applications in studying the aging process and preserving neural integrity. Evidentially, it possesses the ability to stimulate sirtuin 1 is an NAD+-dependent enzyme, thereby augmenting mitochondrial functionality and fortifying cellular energy metabolism. Synonyms: 3-Carbamoyl-1-a-D-ribofuranosylpyridinium hydroxide,5'-phosphate, inner salt; α-nicotinamide mononucleotide; α-Nicotinamid-nucleotid; 3-carbamoyl-1-(O5-phosphono-α-D-ribofuranosyl)-pyridinium betaine; ((2R,3S,4R,5S)-5-(3-carbamoylpyridinium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen phosphate. CAS No. 7298-94-4. Molecular formula: C11H15N2O8P. Mole weight: 334.22.
Anti-Cyclic Nucleotide-Gated Cation Channel 2 antibody produced in rabbit
β-NADH, Reduced Disodium Salt (Nicotinamide Adenine Dinucleotide)
Beta-nicotinamide adenine dinucleotide hydrate. Can be used as a cofactor in reactions with NAD-dependent histone deacetylase enzymes.NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron tran...accomplished by the removal of hydrogen atoms. Both of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. Group: Biochemicals. Alternative Names: β-DPNH; β-NADH; DPNH; Diphosphopyridine nucleotide, reduced form; NADH. Grades: Highly Purified. CAS No. 606-68-8. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C21H27N7O14P2Na2, Molecular Weight: 709.41. US Biological Life Sciences.
Worldwide
β-Nicotinamide-Adenine Dinucleotide, Oxidized Form (NAD)
Nicotinamide adenine dinucleotide (NAD) is a coenzyme found in all living cells. The compound is a dinucleotide, because it consists of two nucleotides joined through their phosphate groups. One nucleotide contains an adenine base and the other nicotinamide. Nicotinamide adenine dinucleotide exists in two forms, an oxidized and reduced form abbreviated as NAD+ and NADH respectively. Group: Coenzymes. Synonyms: β-DPN; β-NAD; Coenzyme 1; Cozymase; DPN; Diphosphopyridine nucleotide; NAD; Nadide; 53-84-9. CAS No. 53-84-9. Purity: > 95%. β-NAD. Mole weight: 663.4 (As anhydrous free acid)681.4 (as monohydrate). Storage: Keep tightly stoppered in the dark below 5°C. Moisture will reduce the purity. For prolonged storage, keep below -20°C. β-DPN; β-NAD; Coenzyme 1; Cozymase; DPN; Diphosphopyridine nucleotide; NAD; Nadide; 53-84-9. Cat No: NATE-0785.
β-Nicotinamide adenine dinucleotide phosphate
β-Nicotinamide adenine dinucleotide 2?-phosphate (NADP+) and β-Nicotinamide adenine dinucleotide 2?-phosphate, reduced (NADPH) comprise a coenzyme redox pair (NADP+:NADPH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. The NADP+/NADPH redox pair facilitates electron transfer in anabolic reactions such as lipid and cholesterol biosynthesis and fatty acyl chain elongation. The NADP+/NADPH redox pair is used in a variety of antioxidation mechanism where it protects agains reactive oxidation species accumulation. NADPH is generated in vivio by the pentose phosphate pathway (PPP). Applications: A common form of nadp. Group: Coenzymes. Synonyms: β-NADP; Coenzyme II; TPN; Codehydrogenase II; NADP; Triphosphopyridine nucleotide; Nicotinamide adenine dinucleotide phosphate hydrate. Enzyme Commission Number: 200-178-1. CAS No. 53-59-8. Purity: > 95%. β-NADP. Mole weight: 743.41. Appearance: Powder. Storage: Store at -20°C. β-NADP; Coenzyme II; TPN; Codehydrogenase II; NADP; Triphosphopyridine nucleotide; Nicotinamide adenine dinucleotide phosphate hydrate. Cat No: NATE-1077.
beta-Nicotinamide adenine dinucleotide phosphate
NADP zwitterion is a NADP. It has a role as a fundamental metabolite. It is a conjugate base of a NADP(+). A coenzyme composed of ribosylnicotinamide 5'-phosphate (NMN) coupled by pyrophosphate linkage to the 5'-phosphate adenosine 2',5'-bisphosphate. It serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH). Synonyms: beta-NADP; NADP; TPN; Triphosphopyridine nucleotide; coenzyme II; Codehydrogenase II; Nadide phosphate; [[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl][(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate. Grades: ≥ 90%. CAS No. 53-59-8. Molecular formula: C21H28N7O17P3. Mole weight: 743.41.
β-Nicotinamide adenine dinucleotide, reduced disodium salt
β-Nicotinamide adenine dinucleotide can be used in enzyme cycling assays to amplify detection of activity of biologically relevant enzymes or metabolites present in low concentrations. Applications: A regenerating electron donor coenzyme. Group: Coenzymes. Synonyms: β-DPNH; β-NADH; DPNH, Diphosphopyridine nucleotide, reduced form; NADH. CAS No. 606-68-8. Purity: ≥94%. Mole weight: 709.4. Appearance: Powder. Form: Solid. β-DPNH; β-NADH; DPNH, Diphosphopyridine nucleotide, reduced form; NADH; β-Nicotinamide adenine dinucleotide, reduced disodium salt; 606-68-8. Cat No: COEC-050.
Beta-Nicotinamide Adenine Dinucleotide Sodium Salt
A metabolite of Nicotine,which is a potent parasympathomimetic stimulant. Synonyms: β-DPN, β-NAD, Coenzyme 1, Cozymase, DPN, Diphosphopyridine nucleotide, NAD, Nadide. Grades: > 95%. CAS No. 20111-18-6. Molecular formula: C21H26N7O14P2. Na. Mole weight: 662.43 22.99.
β-Nicotinamide Adenine Dinucleotide Sodium Salt Hydrate
β-Nicotinamide Adenine Dinucleotide is a coeznyme consisting of an adenine base and a nicotinamide base connected by a pair of bridging phosphate group. β-Nicotinamide Adenine Dinucleotide acts as a coenzyme in redox reactions, as a donor of ADP-ribose moieties in ADP-ribosylation reactions and also as a precursor of the second messenger molecule cyclic ADP-ribose. β-Nicotinamide Adenine Dinucleotide also acts as a substrate for bacterial DNA ligases and a group of enzymes called sirtuins that use NAD+ to remove acetyl groups from proteins. Synonyms: Adenosine 5'-(Trihydrogen Diphosphate), P'?5'-Ester with 3-(Aminocarbonyl)-1-β-D-ribofuranosylpyridinium Hydroxide Sodium Salt Hydrate; Adenine-nicotinamide Dinucleotide Sodium Salt Hydrate; CO-I Sodium Salt Hydrate; Codehydrase I Sodium Salt Hydrate; Codehydrogenase I Sodium Salt Hydrate; Coenzyme I Sodium Salt Hydrate; Cozymase I Sodium Salt Hydrate; DPN Sodium Salt Hydrate; Diphosphopyridine Nucleotide Sodium Salt Hydrate; Enzopride Sodium Salt Hydrate; NAD Sodium Salt Hydrate; NAD+ Sodium Salt Hydrate; NSC 20272 Sodium Salt Hydrate; Nadide Sodium Salt Hydrate; Nicotinamide-adenine Dinucleotide Sodium Salt Hydrate; Oxidized diphosphopyridine Nucleotide Sodium Salt Hydrate; β-Diphosphopyridine Nucleotide Sodium Salt Hydrate; β-NAD Sodium Salt Hydrate; β-NAD+ Sodium Salt Hydrate. Grades: 95%. Molecular formula: C21H26N7NaO14P2 X(H2O). Mole weight: 685.41.
β-Nicotinamide Mononucleotide
Nicotinamide mononucleotide ("NMN" and "β-NMN") is a nucleotide derived from ribose and nicotinamide. Niacinamide (nicotinamide,) is a derivative of vitamin B3, also known as niacin.) As a biochemical precursor of NAD+, it may be useful in the prevention of pellagra. Group: Coenzymes. Synonyms: β-NMN; β-Nicotinamide ribose monophosphate; NMN; Nicotinamide ribotide; Nicotinamide-1-ium-1-β-D-ribofuranoside 5'-phosphate. CAS No. 1094-61-7. Purity: >98%. Mole weight: 334.2 (as anhydrous free acid); 357.2 (as monosodium anhydrate). Storage: Keep dry and away from light, long term storage at -25°C to -15°C. Form: White to Yellowish lyophilized powder. β-NMN; β-Nicotinamide ribose monophosphate; NMN; Nicotinamide ribotide; Nicotinamide-1-ium-1-β-D-ribofuranoside 5'-phosphate. Cat No: COE-001.
β-Nicotinic Acid Mononucleotide
A nucleotide of nicotinic acid which is produced from quinolinic acid by quinolinate phosphoribosyl transferase via transfer of a phosphoribose group. It is an intermediate of nicotinic acid adenine dinucleotide (NaAD) which is then converted to NAD via amidation and in turn converted to NADPH. Group: Biochemicals. Alternative Names: 3-Carboxy-1-(5-O-phosphono- β -D-ribofuranosyl) pyridinium Inner Salt; 3-Carboxy-1- β -D-ribofuranosyl pyridinium Hydroxide 5'-Phosphate Inner Salt; Nicotinate Mononucleotide; Nicotinate Ribonucleotide; Nicotinic Acid Ribonucleotide; Nicotinic Acid Ribotide; Nicotinic Mononucleotide; β-NaMN. Grades: Highly Purified. CAS No. 321-02-8. Pack Sizes: 1mg, 5mg, 10mg. US Biological Life Sciences.
Worldwide
β-Nicotinic Acid Mononucleotide
A nucleotide of nicotinic acid which is produced from quinolinic acid by quinolinate phosphoribosyltransferase via transfer of a phosphoribose group. It is an intermediate of nicotinic acid adenine dinucleotide (NaAD) which is then converted to NAD via amidation and in turn converted to NADPH. Synonyms: 3-Carboxy-1-(5-O-phosphono-β-D-ribofuranosyl)pyridinium Inner Salt; 3-Carboxy-1-β-D-ribofuranosylpyridinium Hydroxide 5'-Phosphate Inner Salt; Nicotinate Mononucleotide; Nicotinate Ribonucleotide; Nicotinic Acid Ribonucleotide; Nicotinic Acid Ribotide; Nicotinic Mononucleotide; β-NaMN. Grades: 95%. CAS No. 321-02-8. Molecular formula: C11H14NO9P. Mole weight: 335.2.
b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate
b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate exemplifies an essential coenzyme that assumes a pivotal function in diverse biochemical reactions. This compound emerges as uniquely advantageous towards interrogating cellular metabolism, enzyme kinetics and redox reactions. Synonyms: coenzyme II; b-NADP-K; Triphosphopyridine nucleotide potassium salt; TPN; [5-(6-aminopurin-9-yl)-3-hydroxy-4-(oxyphosphinyloxyphosphinyl)oxolan-2-yl]met hyl{[5- (3-carbamoylpyridyl)-3, 4-dihydroxyoxolan-2-yl]methoxy} (hydroxyphosphoryl)hydrogen phosphate,potassium salt; Beta-nadp potassium salt; Nadp monopotassium salt. Grades: ≥ 90%. CAS No. 68141-45-7. Molecular formula: C21H27KN7O17P3. Mole weight: 781.50.
b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate
b-Nicotinamide adenine dinucleotide phosphate potassium salt hydrate. Group: Biochemicals. Alternative Names: coenzyme II; b-NADP-K; Triphosphopyridine nucleotide potassium salt; TPN. Grades: Highly Purified. CAS No. 68141-45-7. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C21H27KN7O17P3. US Biological Life Sciences.
Worldwide
b-Nicotinamide Adenine Dinucleotide Phosphate, reduced form, tetrasodium salt ( β-NADPH)
One of the biologically active forms of nicotinic acid. Differs from NAD by an additional phosphate group at the 2-position of the adenosine moiety. Serves as a coenzyme of hydrogenases and dehydrogenases. Present in living cells primarily in the reduced form (NADPH) and is involved in synthetic reactions. Group: Biochemicals. Alternative Names: 2'-(Dihydrogen Phosphate) 5'-(Trihydrogen Pyrophosphate) adenosine 5'5'-Ester 1,4-Dihydro-1- β -D-ribofuranosyl nicotinamide Tetrasodium Salt Hydrate; β-NADPH; 2?-NADPH Hydrate; Coenzyme II Reduced Tetrasodium Salt Hydrate; Triphosphopyridine Nucleotide Reduced Tetrasodium Salt Hydrate; Dihydronicotinamide Adenine Dinucleotide Phosphate Tetrasodium Salt Hydrate. Grades: Highly Purified. CAS No. 2646-71-1. Pack Sizes: 100mg, 250mg, 500mg, 1g. Molecular Formula: C??H??N?Na?O??P?; xH?O, Molecular Weight: 833.35. US Biological Life Sciences.
Worldwide
HCN4 Control Peptide (Hyperpolarization-activated Cyclic Nucleotide-gated Potassium Channel 4)
HCN4 Control Peptide (Hyperpolarization-activated Cyclic Nucleotide-gated Potassium Channel 4). Group: Molecular Biology. Pack Sizes: 120ug. US Biological Life Sciences.
Beta-nicotinamide adenine dinucleotide hydrate. Can be used as a cofactor in reactions with NAD-dependent histone deacetylase enzymes.NAD is a coenzyme formed from the nucleotide, nicotinamide, adenosine monophosphateand a phosphate group joining the first two components. NADP has the same structure with the addition of an extra phosphate group to AMP. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. For example, the reaction catalyzed by glyceraldehyde phosphate dehydrogenase during glycolysis. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron transp...oth of these coenzymes play crucial roles in this. Each molecule of NAD+ (or NADP+) can acquire two electrons; that is, be reduced by two electrons. However, only one proton accompanies the reduction. The other proton produced as two hydrogen atoms are removed from the molecule being oxidized is liberated into the surrounding medium. For NAD, the reaction is thus:NAD+ + 2H -> NADH + H+. Group: Biochemicals. Alternative Names: Nicotinamide Adenine Dinucleotide; Thio-NADH; Thionicotinamide adenine dinucleotide. Grades: Highly Purified. CAS No. 1921-48-8. Pack Sizes: 100mg. Molecular Formula: C21H29N7O13SP2, Molecular Weight: 681.51. US Biological Life Sciences.
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Applications: The enzyme is useful for the preparation of polyribonucleotide. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Mole weight: 300,000 - 340,000; Subunit molecular weight : ca. 85,000. Appearance: Lyophilized. Storage: Stable at -20 °C for at least one year. Source: Bacillus stearothermophilus. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-1908.
Hydrolyzes the 3',5'-phosphodiester bond in cyclic nucleotide monophosphates, such as cAMP and cGMP, to the corresponding nucleotide 5'-monophosphate. Applications: Cyclic nucleotide phosphodiesterase has been investigated for its mechanism of activation as a function of calmodulin and ca2+. it has also been used in a study to show that the binding of trifluoperazine to the activator of cyclic nucleotide phosphodiesterase increases the activity by over 10-fold. for use in calmodulin (p 0270) assay. activity is reduced to <50% without calmodulin present. Group: Enzymes. Synonyms: cyclic 3',5'-mononucleotide phosphodiesterase; PDE; cyclic 3',5'-nucleotide ...th added activator). Storage: -20°C. Form: lyophilized powder (contains imidazole buffer salts and magnesium sulfate). Source: Bovine heart. Species: Bovine. cyclic 3',5'-mononucleotide phosphodiesterase; PDE; cyclic 3',5'-nucleotide phosphodiesterase; cyclic 3',5'-phosphodiesterase; 3',5'-nucleotide phosphodiesterase; 3':5'-cyclic nucleotide 5'-nucleotidohydrolase; 3',5'-cyclonucleotide phosphodiesterase; cyclic nucleotide phosphodiesterase; 3', 5'-cyclic nucleoside monophosphate phosphodiesterase; 3':5'-monophosphate phosphodiesterase (cyclic CMP); cytidine 3':5'-monophosphate phosphodiesterase (cyclic CMP); cyclic 3',5-nucleotide monophosphate phosphod
In enzymology, a nucleotide diphosphatase (EC 3.6.1.9) is an enzyme that catalyzes the chemical reaction:a dinucleotide + H2O<-> 2 mononucleotides. Thus, the two substrates of this enzyme are dinucleotide and H2O, whereas its product is mononucleotide. This enzyme belongs to the family of hydrolases, specifically those acting on acid anhydrides in phosphorus-containing anhydrides. This enzyme participates in 5 metabolic pathways:purine metabolism, starch and sucrose metabolism, riboflavin metabolism, nicotinate and nicotinamide metabolism, and pantothenate and coa biosynthesis. Group: Enzymes. Synonyms: nucleotide diphosphatase; EC 3.6.1.9; nucleotide pyrophosphatase; nucleotide-sugar pyrophosphatase; 9032-64-8. Enzyme Commission Number: EC 3.6.1.9. CAS No. 9032-64-8. Nucleotide Pyrophosphatase. Activity: 4-8 units/mg protein, vial of ~25 units. Storage: -20°C. Form: Lyophilized powder containing approx. 35% Tris buffer salts. Source: Crotalus adamanteus venom. nucleotide diphosphatase; EC 3.6.1.9; nucleotide pyrophosphatase; nucleotide-sugar pyrophosphatase; 9032-64-8. Pack: vial of ~25 units. Cat No: NATE-0493.
PDE3 is a phosphodiesterase. The PDEs belong to at least eleven related gene families, which are different in their primary structure, substrate affinity, responses to effectors, and regulation mechanism. Most of the PDE families are composed of more than one gene. PDE3 is clinically significant because of its role in regulating heart muscle, vascular smooth muscle and platelet aggregation. PDE3 inhibitors have been developed as pharmaceuticals, but their use is limited by arrhythmic effects and they can increase mortality in some applications. Applications: May be used to assay the protein activator, calmodulin. Group: Enzymes. Synonyms: cyclic 3',5'-m...finity chromatography. PDE. Mole weight: mol wt ~60 kDa. Storage: -20°C. Form: Lyophilized preparation which has been depleted of calmodulin and containing buffer salts as Tris-HCl. Source: Porcine brain. Species: Porcine. cyclic 3',5'-mononucleotide phosphodiesterase; PDE; cyclic 3',5'-nucleotide phosphodiesterase; cyclic 3',5'-phosphodiesterase; 3',5'-nucleotide phosphodiesterase; 3':5'-cyclic nucleotide 5'-nucleotidohydrolase; 3',5'-cyclonucleotide phosphodiesterase; cyclic nucleotide phosphodiesterase; 3', 5'-cyclic nucleoside monophosphate phosphodiesterase; 3':5'-monophosphate phosphodiesterase (cyclic CMP); cytidine 3':5'-monophosphate phosphodie
This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). This enzyme participates in nicotinate and nicotinamide metabolism. The human version of this protein is NMNAT1. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Drug development; medicine. Group: Enzymes. Synonyms: NAD + pyrophosphorylase; adenosine triphosphate-nicotinamide mononucleotide transadenylase; ATP:NMN adenylyltransferase; diphosphopyridine nucleotide pyrophosphorylase; nicotinamide adenine dinucleotide pyrophosphorylase; nicotinamide mononucleotide adenylyltransferase; NMN adenylyltransferase. Enzyme Commission Number: EC 2.7.7.1. CAS No. 9032-70-6. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. NAD + pyrophosphorylase; adenosine triphosphate-nicotinamide mononucleotide transadenylase; ATP:NMN adenylyltransferase; diphosphopyridine nucleotide pyrophosphorylase; nicotinamide adenine dinucleotide pyrophosphorylase; nicotinamide mononucleotide adenylyltransferase; NMN adenylyltransferase. Pack: 100ml. Cat No: NATE-1830.
nicotinamide-nucleotide adenylyltransferase
Nicotinate nucleotide can also act as acceptor. See also EC 2.7.7.18 nicotinate-nucleotide adenylyltransferase. Group: Enzymes. Synonyms: NAD+ pyrophosphorylase; adenosine triphosphate-nicotinamide mononucleotide transadenylase; ATP:NMN adenylyltransferase; diphosphopyridine nucleotide pyrophosphorylase; nicotinamide adenine dinucleotide pyrophosphorylase; nicotinamide mononucleotide adenylyltransferase; NMN adenylyltransferase. Enzyme Commission Number: EC 2.7.7.1. CAS No. 9032-70-6. 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-3225; nicotinamide-nucleotide adenylyltransferase; EC 2.7.7.1; 9032-70-6; NAD+ pyrophosphorylase; adenosine triphosphate-nicotinamide mononucleotide transadenylase; ATP:NMN adenylyltransferase; diphosphopyridine nucleotide pyrophosphorylase; nicotinamide adenine dinucleotide pyrophosphorylase; nicotinamide mononucleotide adenylyltransferase; NMN adenylyltransferase. Cat No: EXWM-3225.
nicotinamide-nucleotide amidase
Also acts more slowly on β-nicotinamide D-ribonucleoside. Group: Enzymes. Synonyms: NMN deamidase; nicotinamide mononucleotide deamidase; nicotinamide mononucleotide amidohydrolase. Enzyme Commission Number: EC 3.5.1.42. CAS No. 37355-58-1. 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-4431; nicotinamide-nucleotide amidase; EC 3.5.1.42; 37355-58-1; NMN deamidase; nicotinamide mononucleotide deamidase; nicotinamide mononucleotide amidohydrolase. Cat No: EXWM-4431.
The enzyme is involved in the biosynthesis of phenolic cobamides in the Gram-positive bacterium Sporomusa ovata. It can also transfer the phospho-D-ribosyl group to 4-methylphenol and 5,6-dimethylbenzimidazole. The related EC 2.4.2.21, nicotinate-nucleotide dimethylbenzimidazole phosphoribosyltransferase, also transfers the phospho-D-ribosyl group from nicotinate D-ribonucleotide to 5,6-dimethylbenzimidazole, but shows no activity with 4-methylphenol or phenol. Group: Enzymes. Synonyms: ArsAB. Enzyme Commission Number: EC 2.4.2.55. 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-2685; nicotinate D-ribonucleotide:phenol phospho-D-ribosyltransferase; EC 2.4.2.55; ArsAB. Cat No: EXWM-2685.
nicotinate-nucleotide adenylyltransferase
This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). The systematic name of this enzyme class is ATP:nicotinate-ribonucleotide adenylyltransferase. Other names in common use include deamido-NAD+ pyrophosphorylase, nicotinate mononucleotide adenylyltransferase, deamidonicotinamide adenine dinucleotide pyrophosphorylase, NaMN-ATase, and nicotinic acid mononucleotide adenylyltransferase. This enzyme participates in nicotinate and nicotinamide metabolism. Group: Enzymes. Synonyms: deamido-NAD+ pyrophosphorylase; nicotinate mononucleotide adenylyltransferase; deamidonicotinamide adenine dinucleotide pyrophosphorylase; NaMN-ATase; nicotinic acid mononucleotide adenylyltransferase. Enzyme Commission Number: EC 2.7.7.18. CAS No. 9026-98-6. 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-3232; nicotinate-nucleotide adenylyltransferase; EC 2.7.7.18; 9026-98-6; deamido-NAD+ pyrophosphorylase; nicotinate mononucleotide adenylyltransferase; deamidonicotinamide adenine dinucleotide pyrophosphorylase; NaMN-ATase; nicotinic acid mononucleotide adenylyltransferase. Cat No: EXWM-3232.
Also acts on benzimidazole, and the clostridial enzyme acts on adenine to form 7-α-D-ribosyladenine 5'-phosphate. The product of the reaction, α-ribazole 5'-phosphate, forms part of the corrin-biosynthesis pathway and is a substrate for EC 2.7.8.26, adenosylcobinamide-GDP ribazoletransferase. It can also be dephosphorylated to form α-ribazole by the action of EC 3.1.3.73, α-ribazole phosphatase. Group: Enzymes. Synonyms: nicotinate mononucleotide-dimethylbenzimidazole phosphoribosyltransferase; nicotinate ribonucleotide:benzimidazole (adenine) phosphoribosyltransferase; nicotinate-nucleotide:dimethylbenzimidazole phospho-D-ribosyltransferase; CobT; nicotinate mononu. Enzyme Commission Number: EC 2.4.2.21. CAS No. 37277-76-2. 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-2649; nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase; EC 2.4.2.21; 37277-76-2; nicotinate mononucleotide-dimethylbenzimidazole phosphoribosyltransferase; nicotinate ribonucleotide:benzimidazole (adenine) phosphoribosyltransferase; nicotinate-nucleotide:dimethylbenzimidazole phospho-D-ribosyltransferase; CobT; nicotinate mononucleotide (NaMN):5,6-dimethylbenzimidazole phosphoribosyltransferase. Cat No: EXWM-2649.
The reaction is catalysed in the opposite direction. Since quinolinate is synthesized from L-tryptophan in eukaryotes, but from L-aspartate in some prokaryotes, this is the first NAD+ biosynthesis enzyme shared by both eukaryotes and prokaryotes. Group: Enzymes. Synonyms: quinolinate phosphoribosyltransferase (decarboxylating); quinolinic acid phosphoribosyltransferase; QAPRTase; NAD+ pyrophosphorylase; nicotinate mononucleotide pyrophosphorylase (carboxylating); quinolinic phosphoribosyltransferase. Enzyme Commission Number: EC 2.4.2.19. CAS No. 37277-74-0. 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-2646; nicotinate-nucleotide diphosphorylase (carboxylating); EC 2.4.2.19; 37277-74-0; quinolinate phosphoribosyltransferase (decarboxylating); quinolinic acid phosphoribosyltransferase; QAPRTase; NAD+ pyrophosphorylase; nicotinate mononucleotide pyrophosphorylase (carboxylating); quinolinic phosphoribosyltransferase. Cat No: EXWM-2646.
Nicotinic Acid Adenine Dinucleotide
Nicotinic Acid Adenine Dinucleotide is an analog of β-Nicotinamide Adenine Dinucleotide; a coenzyme consisting of an adenine base and a nicotinamide base connected by a pair of bridging phosphate groups. β-Nicotinamide Adenine Dinucleotide acts as a coenzyme in redox reactions, as a donor of ADP-ribose moieties in ADP-ribosylation reactions and also as a precursor of the second messenger molecule cyclic ADP-ribose. β-Nicotinamide Adenine Dinucleotide also acts as a substrate for bacterial DNA ligases and a group of enzymes called sirtuins that use NAD+ to remove acetyl groups from proteins. Synonyms: Adenosine 5'-(trihydrogen diphosphate), P'?5'-ester with 3-carboxy-1-β-D-ribofuranosylpyridinium, inner salt; 3-Carboxy-1-β-D-ribofuranosylpyridinium hydroxide, 5'-ester with adenosine 5'-pyrophosphate, inner salt; Pyridinium, 3-carboxy-1-β-D-ribofuranosyl-, hydroxide, 5'?5'-ester with adenosine 5'-(trihydrogen pyrophosphate), inner salt; 1: PN: WO2006081329 PAGE: 47 claimed sequence; Adenine-nicotinic Acid Dinucleotide; Codehydrogenase I, carboxy deamido analog; Codehydrogenase I, nicotinic acid analog; Deamido-NAD; Deamidodiphosphopyridine Nucleotide; Desamido NAD; Nicotinate Adenine Dinucleotide; Nicotinic Acid-adenine Dinucleotide. CAS No. 6450-77-7. Molecular formula: C21H26N6O15P2. Mole weight: 664.41.
polynucleotide adenylyltransferase
Also acts slowly with CTP. Catalyses template-independent extension of the 3'- end of a DNA strand by one nucleotide at a time. Cannot initiate a chain de novo. The primer, depending on the source of the enzyme, may be an RNA or DNA fragment, or oligo(A) bearing a 3'-OH terminal group. See also EC 2.7.7.6 DNA-directed RNA polymerase. Group: Enzymes. Synonyms: NTP polymerase; RNA adenylating enzyme; AMP polynucleotidylexotransferase; ATP-polynucleotide adenylyltransferase; ATP:polynucleotidylexotransferase; poly(A) polymerase; poly(A) synthetase; polyadenylate nucleotidyltransferase; polyadenylate polym. Enzyme Commission Number: EC 2.7.7.19. CAS No. 9026-30-6. 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-3233; polynucleotide adenylyltransferase; EC 2.7.7.19; 9026-30-6; NTP polymerase; RNA adenylating enzyme; AMP polynucleotidylexotransferase; ATP-polynucleotide adenylyltransferase; ATP:polynucleotidylexotransferase; poly(A) polymerase; poly(A) synthetase; polyadenylate nucleotidyltransferase; polyadenylate polymerase; polyadenylate synthetase; polyadenylic acid polymerase; polyadenylic polymerase; terminal riboadenylate transferase; poly(A) hydrolase; RNA formation factors, PF1; adenosine triphosphate:ribonucleic acid adenylyltransferase. Cat No: EXWM-3233.
Polynucleotide Phosphorylase from Escherichia coli, Recombinant
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Applications: Polynucleotide phosphorylase (pnp) has been used in a study to show that spontaneous mutations resulting from replication errors are reduced in a pnp-deficient strain. it has also been used in a study to show that the absence of pnpase makes e. coli cells sensitive to uv, which suggests pnp has a role in survival of uv damage. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Storage: -70°C. Form: Supplied as a solution in 20 mM Hepes buffer pH 7.9, 0.1 mM EDTA, 2 mM DTT, 12.5 mM MgCl2, 200 mM KCl, 21.4% (w/v) Glycerol. Source: E. coli. Species: Escherichia coli. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-0608.
Polynucleotide phosphorylase from Human, Recombinant
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Storage: -70°C. Form: supplied as a solution in 20 mM HEPES buffer, pH 7.9, with 0.1 mM EDTA, 2 mM DTT, 12.5 mM MgCl2, ~130 mM KCl, and 20% (w/v) glycerol. Source: E. coli. Species: Human. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-0609.
Polynucleotide phosphorylase from Synechocystis sp., Recombinant
Polynucleotide phosphorylase (PNPase) is a bifunctional enzyme with a phosphorolytic 3' to 5' exoribonuclease activity and a 3'-terminal oligonucleotide polymerase activity. It is also involved in mRNA processing and degradation in bacteria, plants, and humans. Polynuclotide phosphorlyase in spinach chloroplasts acts as a exonuclease and a poly (a) polymerase. Applications: Polynucleotide phosphorylase has been used in a study to discover that a major function of pnpase is the synthesis of cdp. it has also been used in a study to investigate the enzyme responsible for rna 3?-tail synthesis in s. coelicolor. Group: Enzymes. Synonyms: PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. Storage: -70°C. Source: E. coli. Species: Synechocystis sp. PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase; EC 2.7.7.8; 9014-12-4. Cat No: NATE-0610.
polyribonucleotide nucleotidyltransferase
ADP, IDP, GDP, UDP and CDP can act as donors. Group: Enzymes. Synonyms: polynucleotide phosphorylase; PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase. Enzyme Commission Number: EC 2.7.7.8. CAS No. 9014-12-4. Polynucleotide phosphorylase. 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-3292; polyribonucleotide nucleotidyltransferase; EC 2.7.7.8; 9014-12-4; polynucleotide phosphorylase; PNPase; nucleoside diphosphate:polynucleotidyl transferase; polyribonucleotide nucleotidyltransferase; polynucleotide phosphorylase; polyribonucleotide phosphorylase. Cat No: EXWM-3292.
[P (R)]-3'-O-[ (1, 1-Dimethylethyl)dimethylsilyl]-5'-O-[ (R)-hydroxymercaptophosphinyl]-P-thioadenylyl- (3'?5')-2'-deoxy-2'-fluoro-, cyclic nucleotide, adenosine, ammonium (1:2) is a potent nucleotide analog used as a therapeutic intervention for the treatment of cancers attributed to abnormal activation of the Ras signaling pathway, including lung cancer and pancreatic cancer. Its mechanism of action involves targeted inhibition of the overactive Ras protein, frequently mutated in these malignancies to curtail pathogenesis. Molecular formula: C26H43FN12O9P2S2Si. Mole weight: 840.86.
pyrimidine-5'-nucleotide nucleosidase
Also acts on dUMP, dTMP and dCMP. Group: Enzymes. Synonyms: pyrimidine nucleotide N-ribosidase; Pyr5N. Enzyme Commission Number: EC 3.2.2.10. CAS No. 9023-31-8. 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-3964; pyrimidine-5'-nucleotide nucleosidase; EC 3.2.2.10; 9023-31-8; pyrimidine nucleotide N-ribosidase; Pyr5N. Cat No: EXWM-3964.
Rho guanine nucleotide exchange factor 17 (425-438) is amino acids 425 to 438 fragment of Rho guanine nucleotide exchange factor 17 which acts as guanine nucleotide exchange factor (GEF) for RhoA GTPases. Synonyms: 164 kDa Rho-specific guanine-nucleotide exchange factor (425-438).
1,1,3,3-Tetrabromoacetone
1,1,3,3-Tetrabromoacetone is an intermediate in the synthesis of 3-Chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone-13C5, which is an isotope labelled Mutagen X (MX) is a chlorinated furanone that accounts for more of the mutagenic activity of drinking water than any other disinfection byproduct. DNA damages provoked by the six mutagens (furylframide, MX, 4-nitroquinoline N-oxide, sodium azide, 1-nitropyrene, and captan) used in the present study have been known to subject to the nucleotide excision repair system. Group: Biochemicals. Grades: Highly Purified. CAS No. 22612-89-1. Pack Sizes: 250mg, 500mg. Molecular Formula: C3H2Br4O. US Biological Life Sciences.
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
11-dATP (Biotin) (Biotin-11-dATP)
Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Alternative Names: g-[N-(Biotin-6-amino-hexanoyl)]-7-propargylamino-2-deoxy-7-deaza-adenosine-5-triphosphate, Triethylammonium Salt. Grades: Highly Purified. Pack Sizes: 10ul. US Biological Life Sciences.
Worldwide
11-dCTP (Biotin)
Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Alternative Names: γ-[N-(Biotin-6-amino-hexanoyl)]-5-propargylamino-2-deoxy-cytidine-5-triphosphate, Triethylammonium Salt. Grades: Highly Purified. CAS No. 136632-30-9. Pack Sizes: 200ul, 5x200ul. Molecular Formula: C28H44N7O16P3S, Molecular Weight: 859.67. US Biological Life Sciences.
Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25ul, 5x25ul. US Biological Life Sciences.
Worldwide
11-dUTP (Biotin) (5mM)
Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Alternative Names: g-[N-(Biotin-6-amino-hexanoyl)]-5-aminoallyl-2-deoxy-uridine-5-triphosphate, Triethylammonium Salt. Grades: Highly Purified. Pack Sizes: 1ml. US Biological Life Sciences.
Biotin-labeled Nucleotides are used for non-fluorescent labeling of nucleic acids in purification and detection applications. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 200ul. US Biological Life Sciences.
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
1,2,3-Tri-O-Acetyl-5-deoxy-D-ribose
1,2,3-Tri-O-Acetyl-5-deoxy-D-ribose is a key intermediate utilized in the biomedicine industry. This compound is commonly employed in the synthesis of nucleotide analogs and antiviral drugs to study various viral infections. Its versatile nature enables the modification and enhancement of drug properties. CAS No. 1234990-04-5. Molecular formula: C11H16O7. Mole weight: 260.24.
1,2-Di-O-acetyl-3-O-benzyl-4-C-(methanesulfonyloxymethyl)-5-O-methanesulfonyl-D-ribofuranose is a synthetically-derived chemical compound that serves as a fundamental precursor for creating nucleotide analogs utilized in the biomedical sector. It has been extensively investigated for its antiviral properties against viruses, including the likes of HIV and hepatitis C.
1',2'-Di-O-acetyl-5'-O-benzoyl-3'-deoxy-3'-fluoro-D-ribofuranose, a compound of immense importance in the biomedical sector, finds diverse applications. Its utility spans extensive usage in research and development to unravel the intricate mechanisms behind nucleosides and nucleotides' synthesis and biological functions. Molecular formula: C16H17FO7. Mole weight: 340.30.
1-(2-Ethoxy-2-oxoethyl)pyridin-1-ium-d5 Chloride
1-(2-Ethoxy-2-oxoethyl)pyridin-1-ium-d5 Chloride is an intermediate used in the synthesis of Girards Reagent P-d5 (G388502), which is a labeled girards reagent used in the identification and quantification of protein carbonylation as well as in the modification of nucleosides and nucleotides. Used in the preparation of potent photoactive agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 1853121-29-5. Pack Sizes: 25mg, 50mg. Molecular Formula: C9H7D5ClNO2, Molecular Weight: 206.68. US Biological Life Sciences.
BODIPY dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, as well as to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres. Synonyms: 4-(4,4-Difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene-8-yl)-butyric Acid. CAS No. 878674-84-1. Molecular formula: C17H22BF2N2O2. Mole weight: 335.18.
1,3,5-Tri-O-acetyl-2-deoxy-D-ribose
1,3,5-Tri-O-acetyl-2-deoxy-D-ribose, a highly sought-after compound in biomedical research, has been utilized extensively for the fabrication of antiviral and antitumor medications, along with its incorporation into nucleotide metabolic studies. The inherent capacity of this compound in impeding the enzymes imperative for viral replication and cancer progression manifests its indispensable role towards the prevention and cure of serious ailments across the globe, ranging from HIV to cancer. CAS No. 4594-52-9. Molecular formula: C11H16O7. Mole weight: 260.24.
1,3,5-Tri-O-benzoyl-2-deoxyribofuranose
1,3,5-Tri-O-benzoyl-2-deoxyribofuranose, a pivotal compound utilized in the realm of biomedicine, assumes a fundamental role in the synthesis of nucleosides and nucleotides for the amelioration of diverse ailments, specifically those associated with DNA replication and mending. Boasting an unparalleled composition, this compound not only embodies high purity but also ubiquity, rendering it an esteemed instrument in the investigation of DNA-related mechanisms and the conception of prospective medicinal remedies. Synonyms: 2-Deoxy-ribose 1,3,5-Tribenzoate. CAS No. 145416-96-2. Molecular formula: C26H22O7. Mole weight: 446.45.
1, 3-Dichloro-1, 1, 3, 3-tetraisopropyl disiloxane is used in the analysis of Watson-Crick and Hoogstein base pairing in nucleotides. Also used in the formation of ribavirin chemical delivery systems. Group: Biochemicals. Alternative Names: 1,1,3,3-Tetraisopropyl-1,3-dichlorodisiloxane; 1, 3-Dichloro-1, 1, 3, 3-tetraisopropyl disiloxane; 1, 3-Dichlorotetraisopropyl disiloxane; TIPDS-Cl2; Tetraisopropyl disiloxane-1, 3-diyl Dichloride. Grades: Highly Purified. CAS No. 69304-37-6. Pack Sizes: 5g. US Biological Life Sciences.
Worldwide
1,4-β-D-xylan synthase
This enzyme belongs to the family of glycosyltransferases, specifically the pentosyltransferases. This enzyme participates in starch and sucrose metabolism and nucleotide sugars metabolism. Group: Enzymes. Synonyms: uridine diphosphoxylose-1,4-β-xylan xylosyltransferase; 1,4-β-xylan synthase; xylan synthase; xylan synthetase; UDP-D-xylose:1,4-β-D-xylan 4-β-D-xylosyltransferase. Enzyme Commission Number: EC 2.4.2.24. CAS No. 37277-73-9. 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-2651; 1,4-β-D-xylan synthase; EC 2.4.2.24; 37277-73-9; uridine diphosphoxylose-1,4-β-xylan xylosyltransferase; 1,4-β-xylan synthase; xylan synthase; xylan synthetase; UDP-D-xylose:1,4-β-D-xylan 4-β-D-xylosyltransferase. Cat No: EXWM-2651.
1-(5',6'-Dideoxy-6'-dimethylphosphono-2'-O-(2-methoxyethyl)-5-methyl-b-D-ribo-hex-5(E)-enofuranosyl)uracil 3'-CE phosphoroamidite is a specialized reagent used in the synthesis of nucleotide analogs. These analogs are vital in the research and development of antiviral drugs, primarily targeting HIV and Hepatitis C. Grades: 98%. Molecular formula: C25H42N4O10P2. Mole weight: 620.57.
1,5-Di-O-acetyl-2,3-O-isopropylidene-D-ribofuranose is a biological reagent playing a role in synthesizing various nucleotide and nucleoside analogs. CAS No. 141979-56-8. Molecular formula: C12H18O7. Mole weight: 274.27.
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