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SELENOUSACID, 65% SOLUTION, 99% pure, 39.8% Se, Formula: H2SeO3. CAS No. 7783-00-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
Texas TX
SelenousAcid
SELENOUSACID, 99% pure, -4 mesh, Formula: H2SeO3. CAS No. 7783-00-8. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
Texas TX
Selenous (Selenous) Acid
Selenous (Selenous) Acid. Group: Biochemicals. Alternative Names: Selenious Acid; Selenium dioxide, hydrated. Grades: Molecular Biology Grade. CAS No. 7783-00-8. Pack Sizes: 25g. Molecular Formula: H2SeO3, Molecular Weight: 128.97. US Biological Life Sciences.
Worldwide
1,7-Dimethyl-9H-fluoren-9-one
1,7-Dimethyl-9H-fluoren-9-one is an intermediate in synthesizing 1,7-Dimethylfluorene (D465730), a product of the selenium dehydrogenation of gibberic acid. 1,7-Dimethylfluorene is also one of the many polyaromatic hydrocarbons (PAH) that are found within lake sediments, negatively impacting zoo plankton changes in the water, as well as the ecosystems that reside there. Group: Biochemicals. Grades: Highly Purified. CAS No. 441-97-4. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C15H12O, Molecular Weight: 208.26. US Biological Life Sciences.
Worldwide
1,7-Dimethylfluorene
1,7-Dimethylfluorene is a product of the selenium dehydrogenation of gibberic acid. 1,7-Dimethylfluorene is also one of the many polyaromatic hydrocarbons (PAH) that are found within lake sediments, negatively impacting zoo plankton changes in the water, as well as the ecosystems that reside there. Group: Biochemicals. Grades: Highly Purified. CAS No. 442-66-0. Pack Sizes: 5mg, 50mg. Molecular Formula: C15H14. US Biological Life Sciences.
Worldwide
2-Methyl-N-[ (4-methylphenyl) sulfonyl]benzamide
2-Methyl-N-[ (4-methylphenyl) sulfonyl]benzamide is an intermediate in synthesizing 1,7-Dimethylfluorene (D465730), a product of the selenium dehydrogenation of gibberic acid. 1,7-Dimethylfluorene is also one of the many polyaromatic hydrocarbons (PAH) that are found within lake sediments, negatively impacting zoo plankton changes in the water, as well as the ecosystems that reside there. Group: Biochemicals. Grades: Highly Purified. CAS No. 146448-53-5. Pack Sizes: 10mg, 25mg. Molecular Formula: C15H15NO3S, Molecular Weight: 289.35. US Biological Life Sciences.
Heterocyclic Organic Compound. CAS No. 1144-33-8. Catalog: ACM1144338.
3-(Methylseleno)-L-alanine
3-(Methylseleno)-L-alanine, a metabolite found in Escherichia coli (strain K12, MG1655), is an inhibitor of DMBA-induced mammary tumors. It has oral bioavailability and can induce cell apoptosis. Synonyms: Se-methylselenocysteine; Methylselenocysteine; (R)-2-Amino-3-(methylselanyl)propanoic acid; Selenium-methylselenocystine. Grades: ≥90%. CAS No. 26046-90-2. Molecular formula: C4H9NO2Se. Mole weight: 182.08.
4-[[2-(1H-Indol-3-yl)ethyl]seleno]butyric acid
Heterocyclic Organic Compound. CAS No. 1148-13-6. Catalog: ACM1148136.
Used in the preparation of Selenobiotin (S248000). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
6-hydroxynicotinate dehydrogenase
Contains [2Fe-2S] iron-sulfur centres, FAD and molybdenum. It also has a catalytically essential, labile selenium that can be removed by reaction with cyanide. In Bacillus niacini, this enzyme is required for growth on nicotinic acid. Group: Enzymes. Synonyms: 6-hydroxynicotinic acid hydroxylase; 6-hydroxynicotinic acid dehydrogenase; 6-hydroxynicotinate hydroxylase; 6-hydroxynicotinate:O2 oxidoreductase. Enzyme Commission Number: EC 1.17.3.3. CAS No. 122191-32-6. 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-1089; 6-hydroxynicotinate dehydrogenase; EC 1.17.3.3; 122191-32-6; 6-hydroxynicotinic acid hydroxylase; 6-hydroxynicotinic acid dehydrogenase; 6-hydroxynicotinate hydroxylase; 6-hydroxynicotinate:O2 oxidoreductase. Cat No: EXWM-1089.
ATP Sulfurylase from S. cerevisiae, Recombinant
In enzymology, a sulfate adenylyltransferase (EC 2.7.7.4) is an enzyme that catalyzes the chemical reaction:ATP + sulfate<-> diphosphate + adenylyl sulfate. Thus, the two substRates of this enzyme are ATP and sulfate, whereas its two products are diphosphate and adenylyl sulfate. This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). This enzyme participates in 3 metabolic pathways:purine metabolism, selenoamino acid metabolism, and sulfur metabolism. Adenosine 5-triphosphate sulfurylase yeast recombinant produced in e. coli is a non-glycosylated, polypeptide chain containin...formed from aps and ppi. adenosine 5-triphosphate sulfurylase is purified by proprietary chromatographic techniques. Group: Enzymes. Synonyms: ATP-sulfurylase; adenosine-5'-triphosphate sulfurylase; adenosinetriphosphate sulfurylase; adenylylsulfate pyrophosphorylase; ATP sulfurylase; sulfurylase; EC 2.7.7.4; 9012-39-9; Sulfate adenylate transferase. CAS No. 9012-39-9. ATP-sulfurylase. Storage: at -20°C. Source: E. coli. Species: S. cerevisiae. ATP-sulfurylase; adenosine-5'-triphosphate sulfurylase; adenosinetriphosphate sulfurylase; adenylylsulfate pyrophosphorylase; ATP sulfurylase; sulfurylase; EC 2.7.7.4; 9012-39-9; Sulfate adenylate transferase. Cat No: NATE-1280.
betaine reductase
The reaction is observed only in the direction of betaine reduction. The enzyme from Eubacterium acidaminophilum consists of subunits A, B and C. Subunit B contains selenocysteine and a pyruvoyl group, and is responsible for betaine binding and trimethylamine release. Subunit A, which also contains selenocysteine, is reduced by thioredoxin, and is needed to convert the carboxymethyl group into a ketene equivalent, in turn used by subunit C to produce acetyl phosphate. Only subunit B distinguishes this enzyme from EC 1.21.4.2 (glycine reductase) and EC 1.21.4.3 (sarcosine reductase). Group: Enzymes. Synonyms: acetyl-phosphate trimethylamine:thioredoxin disulfide oxidoreductase (N,N,N-trimethylglycine-forming). Enzyme Commission Number: EC 1.21.4.4. CAS No. 125752-87-6. 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-1259; betaine reductase; EC 1.21.4.4; 125752-87-6; acetyl-phosphate trimethylamine:thioredoxin disulfide oxidoreductase (N,N,N-trimethylglycine-forming). Cat No: EXWM-1259.
BIS(1-BUTYLPENTYL) DECANE-1,10-DIYL DIGLUTARATE
Abbreviated as Sec or U, in older publications also as Se-Cys, as a building block of selenoproteins, this 21st proteinogenic amino acid exists naturally in three domains of life, but not in every lineage. Uses: Used for the characterization of total sodium concentration in human blood plasma; also used for the preparation of nitrite-selective membrane electrode, used for the potentiometric determination of nad(p)h coenzymes. Synonyms: 5-O-nonan-5-yl 1-O-[10-(5-nonan-5-yloxy-5-oxopentanoyl)oxydecyl] pentanedioate; ETH 469; AC1ND8J0; 30585_FLUKA; ETH-469; ZINC100650269; 5-O-nonan-5-yl 1-O-[10-(5-nonan-5-yloxy-5-oxopentanoyl)oxydecyl] pentanedioate. Grades: ≥ 95.0%. CAS No. 101342-76-1. Molecular formula: C38H70O8. Mole weight: 654.96.
Captopril EP Impurity D
3-Bromo-2-methylpropionic Acid is used in the preparation of captopril selenium analogs as antioxidants and ACE inhibitors used as antihypertensive drugs. Synonyms: (±)-3-Bromo-2-methylpropionic acid; NSC 201472; β-Bromoisobutanoic Acid. Grades: > 95%. CAS No. 56970-78-6. Molecular formula: C4H7BrO2. Mole weight: 167.
CdSeTe/ZnS Quantum Dots
We manufacture near-infrared (near-IR) CdSeTe/ZnS Quantum Dots with narrow band fluorescent emission wavelengths ranging from 700-880 nm. Our organic soluble CdSeTe/ZnS QDs are coated with lipophobic surfactants, while our dispersible, water soluble QDs are coated with hydrophilic surfactants with acid (-COOH), amine (-NH2), or diol (-CHOH-C2OH) terminal end groups. Group: other quantum dots. Alternative Names: Near Infrared (NIR) CdSeTe/ZnS QDs, CdSeTe/ZnS core/shell quantum dots, cadmium selenide telluride/zinc sulfide quantum dots, cd se te zn s quantum dots, cdsete zns quantum dots. Molecular formula: ~1.8x105-~2.8x106g/mol. Mole weight: CdSeTe/ZnS. CdSeTe/ZnSQuantumDots-700nm|CdSeTe/ZnSQuantumDots-720nm|CdSeTe/ZnSQuantumDots-760nm|CdSeTe/ZnSQuantumDots-780nm|CdSeTe/ZnSQuantumDots-820nm|CdSeTe/ZnSQuantumDots-840nm|CdSeTe/ZnSQuantumDots-860nm|CdSeTe/ZnSQuantumDots-880nm.
Cyclohexanone Monooxygenase from Acinetobacter sp., Recombinant
Purified cyclohexanone monooxygenase is a versatile oxygenation catalyst. The enzyme uses the bound FAD-4a-OOH oxygenating intermediate to initiate transfer of oxygen to electrophilic substrate sites. The reaction consequently yields the corresponding sulfoxide and selenoxide products. This enzyme is also capable of oxygenating at nitrogen, trivalent phosphorus, and boron sites in boronic acids. Hence, it is one of the most broad-based flavoprotein oxygenases known. Applications: Cyclohexanone monooxygenase has been used in a study that cloned and overexpressed the 2-oxo-δ(3)-4,5,5-trimethylcyclopentenylacetyl-coa monooxygenase (otemo) in escherichia col....22; 52037-90-8; cyclohexanone,NADPH:oxygen oxidoreductase (lactone-forming). Enzyme Commission Number: EC 1.14.13.22. CAS No. 52037-90-8. Cyclohexanone Monooxygenase. Mole weight: 59 kDa. Activity: >12 U/ml. Storage: Store at -20°C. Form: Suspension in 80% saturated ammonium sulfate, 20 mM K-Na-phosphate buffer pH 7, 3.5 mM 1,4-Dithioerythritol (DTE). Source: E. coli. Species: Acinetobacter sp. yclohexanone 1,2-monooxygenase; cyclohexanone oxygenase; cyclohexanone:NADPH:oxygen oxidoreductase (6-hydroxylating, 1,2-lactonizing); cyclohexanone monooxygenase; EC 1.14.13.22; 52037-90-8; cyclohexanone,NADPH:oxygen oxidoreductase (lactone-forming). Cat No: NATE-0822.
Fmoc-selenomethionine can be introduced under standard conditions. Any selenoxide formed during synthesis can be easily reduced back to selenide by treatment with β-mercaptoethanol. Introduction of selenium can help facilitate solid phase and solution structural determination and the study of peptide-protein interactions. Uses: Fmoc solid-phase peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-selenomethionine, N-Fmoc-L-amino-4-(methylselanyl)butanoic acid. CAS No. 1217852-49-7. Molecular formula: C20H21NO4Se. Mole weight: 418.4. Purity: Peak Area by HPLC ≥95%. Catalog: ACM1217852497.
Fmoc-Sec(pMeOBzl)-OH
Building block for the introduction of selenocysteine during Fmoc SPPS. Selenocysteine derivatives can undergo enantiomerization during coupling and can form dehydroalanine and β-piperidinylalanine containing side products during subsequent chain elongation. Therefore, activation methods, such as HBTU or PyBOP which involve the addition of a tertiary, base should be avoided for addition of the Sec and all subsequent residues. Cleavage and side-chain deprotection of Sec-containing peptides can be effected using tFA-m-cresol-thioanisole-EDT-water (80:5:5:5:5) or TFA-water-DCM-TIS (89:5:51) at 4 °C. As the Se-pMeOBzl bond is stable to TFA, these methods result in the formation of the corresponding Sev(pMeOBzl) peptide. Peptides containing two Sec(pMeOBzl) residues can be oxidized directly to the corresponding selenocystinyl peptides by treatment with 5-10% DMSO in TFA. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Sec(pMeOBzl)-OH, Fmoc-Sec(Mob)-OH, Fmoc-S-4-methoxybenzyl selenocysteine. CAS No. 150308-80-8. Molecular formula: C26H25NO5Se. Mole weight: 510.44. Catalog: ACM150308808.
glycine reductase
The reaction is observed only in the direction of glycine reduction. The enzyme from Eubacterium acidaminophilum consists of subunits A, B and C. Subunit B contains selenocysteine and a pyruvoyl group, and is responsible for glycine binding and ammonia release. Subunit A, which also contains selenocysteine, is reduced by thioredoxin, and is needed to convert the carboxymethyl group into a ketene equivalent, in turn used by subunit C to produce acetyl phosphate. Only subunit B distinguishes this enzyme from EC 1.21.4.3 (sarcosine reductase) and EC 1.21.4.4 (betaine reductase). Group: Enzymes. Enzyme Commission Number: EC 1.21.4.2. CAS No. 39307-24-9. 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-1257; glycine reductase; EC 1.21.4.2; 39307-24-9. Cat No: EXWM-1257.
L-Selenomethionine is the predominant food form of selenium with antioxidant activity. L-Selenomethionine has been shown to increase the activity of glutathione peroxidase in endothelial cells. It may be chemoprotective against certain cancers. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Selenomethionine; L-(+)-Selenomethionine; Selenium-L-methionine; L-Selenomethioninum; Seleno-L-methionine; H-Mse-OH; (2S)-2-amino-4-methylselanylbutanoic acid. Grades: 95%. CAS No. 3211-76-5. Molecular formula: C5H11NO2Se. Mole weight: 196.12.
L-(+)-Selenomethionine
1g Pack Size. Group: Amino Acids, Biochemicals, Chiral Compounds. Formula: C5H11NO2Se. CAS No. 3211-76-5. Prepack ID 24764032-1g. Molecular Weight 196.11. See USA prepack pricing.
L-(+)-Selenomethionine
Seleniated Detergents. Alternative Names: (S)-2-Amino-4-(methylseleno)butyric acid. CAS No. 3211-76-5. Molecular formula: C5H11NO2Se. Mole weight: 196.1. Appearance: White to off white powder. Purity: ≥98%. IUPACName: (2S)-2-amino-4-methylselanylbutanoic acid.
Magnesium Monoperoxyphthalic Acid Hexahydrate
Magnesium Monoperoxyphthalic Acid Hexahydrate is used as an oxidant in various synthetic reactions. For example: it is a mild and efficient oxidant for the synthesis of selenones which are useful synthetic intermediates in the synthesis of different heterocyclic compounds. Group: Biochemicals. Grades: Highly Purified. CAS No. 84665-66-7. Pack Sizes: 50g, 100g. Molecular Formula: C16H22MgO16. US Biological Life Sciences.
Worldwide
MJ33 lithium salt
MJ33 is a selective and reversible inhibitor of the acidic, calcium-independent (ai)PLA2 activity of Prdx6. Prdx6 is a bifunctional enzyme with both non-selenium glutathione peroxidase (Gpx) and PLA2 activities. Synonyms: 1-Hexadecyl-3-(trifluoroethyl)-sn-glycero-2-phosphomethanol, Li. Grades: ≥95%. CAS No. 1007476-63-2. Molecular formula: C22H43F3LiO6P. Mole weight: 498.5.
Native Escherichia coli Thioredoxin Reductase
Thioredoxin reductase (TrxR) is an NADPH-dependent oxidoreductase containing one FAD per subunit that reduces the active site disulfide in oxidised thioredoxin (Trx). The molecular weight of the isozymes from mammalian sources vary between 55-67 kDa as compared with 35 kDa in prokaryotes, plants or yeast. The substrate specificity of the mammalian enzyme is much broader than the prokaryotic enzyme reducing both mammalian and E. coli thioredoxins as well as well as non-disulfide substrates such selenite, lipoic acids, lipid hydroperoxides and hydrogen peroxide. Applications: Thioredoxin reductase from escherichia coli can be used in peroxidase-coupled thioredoxin system assay for assessing the peroxidase activitiy of cys-based thiol peroxidases. the product was used for determining the enzymatic activity of his6-ahp1p. Group: Enzymes. Synonyms: NADP-thioredoxi. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. Activity: >25 units/mg protein (Bradford). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.6 M (NH4)2SO4 containing 30 mM potassium phosphate buffer, pH 7.5, and 2 mM EDTA. Source: Escherichia coli. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR. Cat No: NATE-0718.
Native Rat Thioredoxin Reductase
Thioredoxin reductase (TrxR) is an NADPH-dependent oxidoreductase containing one FAD per subunit that reduces the active site disulfide in oxidised thioredoxin (Trx). The molecular weight of the isozymes from mammalian sources vary between 55-67 kDa as compared with 35 kDa in prokaryotes, plants or yeast. The substrate specificity of the mammalian enzyme is much broader than the prokaryotic enzyme reducing both mammalian and E. coli thioredoxins as well as well as non-disulfide substrates such selenite, lipoic acids, lipid hydroperoxides and hydrogen peroxide. Applications: Thioredoxin reductase from rat liver can be used for studying the uptake and reduction of a-lipoic acid... NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR; 9074-14-0. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. Activity: > 100 units/mg protein (Bradford). Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50 mM Tris-HCl, pH 7.5, 300 mM NaCl, 1 mM EDTA, and 10% glycerol. Source: Rat liver. Species: Rat. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR; 9074-14-0. Cat No: NATE-0713.
In enzymology, a sulfate adenylyltransferase (EC 2.7.7.4) is an enzyme that catalyzes the chemical reaction:ATP + sulfate<-> diphosphate + adenylyl sulfate. Thus, the two substRates of this enzyme are ATP and sulfate, whereas its two products are diphosphate and adenylyl sulfate. This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). This enzyme participates in 3 metabolic pathways:purine metabolism, selenoamino acid metabolism, and sulfur metabolism. Applications: Adenosine-5?-triphosphate sulfurylase (atp sulfurylase) may be used to study sulfur metabolism and h...s. Synonyms: ATP-sulfurylase; adenosine-5'-triphosphate sulfurylase; adenosinetriphosphate sulfurylase; adenylylsulfate pyrophosphorylase; ATP sulfurylase; sulfurylase; EC 2.7.7.4; 9012-39-9; Sulfate adenylate transferase. Enzyme Commission Number: EC 2.7.7.4. CAS No. 9012-39-9. ATP-sulfurylase. Activity: > 1.0 units/mg protein. Storage: -20°C. Form: lyophilized powder. Contains Citrate buffer salts. Source: Saccharomyces cerevisiae. ATP-sulfurylase; adenosine-5'-triphosphate sulfurylase; adenosinetriphosphate sulfurylase; adenylylsulfate pyrophosphorylase; ATP sulfurylase; sulfurylase; EC 2.7.7.4; 9012-39-9; Sulfate adenylate transferase. Cat No: NATE-0090.
nicotinate dehydrogenase
A flavoprotein containing non-heme iron. The enzyme is capable of acting on a variety of nicotinate analogues to varying degrees, including pyrazine-2-carboxylate, pyrazine 2,3-dicarboxylate, trigonelline and 6-methylnicotinate. The enzyme from Clostridium barkeri also possesses a catalytically essential, labile selenium that can be removed by reaction with cyanide. Group: Enzymes. Synonyms: nicotinic acid hydroxylase; nicotinate hydroxylase. Enzyme Commission Number: EC 1.17.1.5. CAS No. 9059-3-4. 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-1083; nicotinate dehydrogenase; EC 1.17.1.5; 9059-03-4; nicotinic acid hydroxylase; nicotinate hydroxylase. Cat No: EXWM-1083.
N,N-Dibenzyl rac Selenobiotin
rac Selenobiotin (S248000) derivative. Group: Biochemicals. Alternative Names: rel-(2S,3S,4R)-Hexahydro-2-oxo-1,3-bis(phenylmethyl)-1H-selenolo[3,4-d]imidazole-4-pentanoic acid. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
O-Phospho-DL-serine
Used in alternative pathways for biosynthesis of cysteine selenocysteine (Sec); Normal metabolites in human biofluids are esters of serine and phosphoric acid. Synonyms: DL-Ser(H2PO3)-OH; DL-Serine monophosphoric acid. Grades: ≥ 98% (Titration). CAS No. 17885-08-4. Molecular formula: C3H8NO6P. Mole weight: 185.10.
A pyridoxal-phosphate protein. In archaea and eukarya selenocysteine formation is achieved by a two-step process: EC 2.7.1.164 (O-phosphoseryl-tRNASec kinase) phosphorylates the endogenous L-seryl-tRNASec to O-phospho-L-seryl-tRNASec, and then this misacylated amino acid-tRNA species is converted to L-selenocysteinyl-tRNASec by Sep-tRNA:Sec-tRNA synthase. Group: Enzymes. Synonyms: MMPSepSecS; SepSecS; SLA/LP; O-phosphoseryl-tRNA:selenocysteinyl-tRNA synthase; O-phospho-L-seryl-tRNA:L-selenocysteinyl-tRNA synthase. Enzyme Commission Number: EC 2.9.1.2. 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-3433; O-phospho-L-seryl-tRNASec:L-selenocysteinyl-tRNA synthase; EC 2.9.1.2; MMPSepSecS; SepSecS; SLA/LP; O-phosphoseryl-tRNA:selenocysteinyl-tRNA synthase; O-phospho-L-seryl-tRNA:L-selenocysteinyl-tRNA synthase. Cat No: EXWM-3433.
O-phosphoseryl-tRNASec kinase
In archaea and eukarya selenocysteine formation is achieved by a two-step process: O-phosphoseryl-tRNASec kinase (PSTK) phosphorylates the endogenous L-seryl-tRNASec to O-phospho-L-seryl-tRNASec, and then this misacylated amino acid-tRNA species is converted to L-selenocysteinyl-tRNASec by EC 2.9.1.2 (Sep-tRNA:Sec-tRNA synthase). Group: Enzymes. Synonyms: PSTK; phosphoseryl-tRNA[Ser]Sec kinase; phosphoseryl-tRNASec kinase. Enzyme Commission Number: EC 2.7.1.164. CAS No. 91273-83-5. 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-2994; O-phosphoseryl-tRNASec kinase; EC 2.7.1.164; 91273-83-5; PSTK; phosphoseryl-tRNA[Ser]Sec kinase; phosphoseryl-tRNASec kinase. Cat No: EXWM-2994.
Selenobiotin as an excretion product of Phycomyces blakesleeanus. It is an excellent growth factor, as efficient as biotin in supporting the growth of biotin-requiring microorganisms. Group: Biochemicals. Alternative Names: Hexahydro-2-oxo-1H-selenolo[3,4-d]imidazole-4-pentanoic Acid. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Rac-Selenobiotin
Selenobiotin as an excretion product of Phycomyces blakesleeanus. It is an excellent growth factor, as efficient as biotin in supporting the growth of biotin-requiring microorganisms. It is a biotin analog. Synonyms: Hexahydro-2-oxo-1H-selenolo[3,4-d]imidazole-4-pentanoic Acid. Grades: > 95%. CAS No. 57956-29-3. Molecular formula: C10H16N2O3Se. Mole weight: 291.21.
sarcosine reductase
The reaction is observed only in the direction of sarcosine reduction. The enzyme from Eubacterium acidaminophilum consists of subunits A, B and C. Subunit B contains selenocysteine and a pyruvoyl group, and is responsible for sarcosine binding and methylamine release. Subunit A, which also contains selenocysteine, is reduced by thioredoxin, and is needed to convert the carboxymethyl group into a ketene equivalent, in turn used by subunit C to produce acetyl phosphate. Only subunit B distinguishes this enzyme from EC 1.21.4.2 (glycine reductase) and EC 1.21.4.4 (betaine reductase). Group: Enzymes. Enzyme Commission Number: EC 1.21.4.3. CAS No. 125752-88-7. 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-1258; sarcosine reductase; EC 1.21.4.3; 125752-88-7. Cat No: EXWM-1258.
selenate reductase
The periplasmic enzyme from Thauera selenatis is a complex comprising three heterologous subunits (α, β and γ) that contains molybdenum, iron, acid-labile sulfide and heme b as cofactor constituents. Nitrate, nitrite, chlorate and sulfate are not substrates. A number of compounds, including acetate, lactate, pyruvate, and certain sugars, amino acids, fatty acids, di- and tricarboxylic acids, and benzoate can serve as electron donors. Group: Enzymes. Enzyme Commission Number: EC 1.97.1.9. CAS No. 146359-71-9. 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-1695; selenate reductase; EC 1.97.1.9; 146359-71-9. Cat No: EXWM-1695.
Selenious acid
Selenious acid. CAS No: 7783-00-8
Sarchem Laboratories New Jersey NJ
Selenious Acid
Reagent for alkaloids, oxidizing agent. Group: Selenium plating chemicals. CAS No. 7783-00-8. ECNumber: 234-974-7. Catalog: ACEP7783008.
Selenious Acid USP
Selenious Acid USP. CAS No. 7783-00-8. Molecular formula: H2SeO3.
Selenium Amino Acid Chelate
Selenium Amino Acid Chelate.
Selenium Shot
Selenium Shot is used in selenium-derived drugs like selenate, selenite, selenomethionine, methyl-selenocysteine (MSC), and methaneselenic acid (MSA), that exhibits anticancer properties clinically by sensitizing p-glycoprotein (p-gp)-overexpressing resistant KBV20C cancer cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 7782-49-2. Pack Sizes: 5g, 25g. Molecular Formula: Se, Molecular Weight: 78.9599999999999. US Biological Life Sciences.
Worldwide
Selenocysteine
Heterocyclic Organic Compound. Alternative Names: (2R)-2-Amino-3-(hydroseleno)propionic acid;3-(Hydroseleno)alanine;3-Selenylalanine;3-Selenyl-L-alanine;Seleno-L-cysteine;(R)-2-aMino-3-hydroselenopropanoic acid;L-Alanine, 3-selenyl-. CAS No. 10236-58-5. Molecular formula: C3H7NO2Se. Mole weight: 168.05. Catalog: ACM10236585.
Selenomethionine
Selenomethionine is a naturally occurring amino acid containing selenium that has oral activity and is a common natural food source. Selenomethionine has antitumor activity [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Seleno-DL-methionine; DL-Selenomethionine. CAS No. 1464-42-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-B1000.
Selenosulfuric Acid Dipotassium Salt
Selenosulfuric Acid Dipotassium Salt is used in the synthesis of CdSe photocatalysts with enhanced photocatalytic ativitys. Possible application towards industrial wastewater treatment and pollutant removal. Group: Biochemicals. Alternative Names: Dipotassium Selenosulfate; potassium selenosulfate; potassium selenosulfate (K2SeSO3). Grades: Purified. CAS No. 15571-89-8. Pack Sizes: 50mg. Molecular Formula: K2O3SSe, Molecular Weight: 237.22. US Biological Life Sciences.
Worldwide
Se-(Methyl)selenocysteine hydrochloride
Se-(Methyl)selenocysteine hydrochloride is an anticancer agent that inhibits cell cycle proliferation and induces apoptosis. Synonyms: (2R)-2-amino-3-methylselanylpropanoic acid hydrochloride; (R)-2-Amino-3-(methylselanyl)propanoic acid hydrochloride; Se-MSC. Grades: >95%. CAS No. 863394-07-4. Molecular formula: C4H10ClNO2Se. Mole weight: 218.55.
serine-tRNA ligase
This enzyme also recognizes tRNASec, the special tRNA for selenocysteine, and catalyses the formation of L-seryl-tRNASec, the substrate for EC 2.9.1.1, L-seryl-tRNASec selenium transferase. Group: Enzymes. Synonyms: seryl-tRNA synthetase; SerRS; seryl-transfer ribonucleate synthetase; seryl-transfer RNA synthetase; seryl-transfer ribonucleic acid synthetase; serine translase. Enzyme Commission Number: EC 6.1.1.11. CAS No. 9023-48-7. 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-5642; serine-tRNA ligase; EC 6.1.1.11; 9023-48-7; seryl-tRNA synthetase; SerRS; seryl-transfer ribonucleate synthetase; seryl-transfer RNA synthetase; seryl-transfer ribonucleic acid synthetase; serine translase. Cat No: EXWM-5642.
98%. Uses: Tdpa can be used to cap copper nanoparticles to protect them from oxidation. it may also be used in the synthesis of cadmium sulfate (cds) core, which can be used in the fabrication of cadmium selenium (cdse)/cds core quantum dots (qds). it may also be coated on caesium lead bromide (cspbbr3) perovskite quantum dots for the development of white light emitting diodes (wled). Group: Self-assembly materials self assembly and contact printing materials. Alternative Names: TPA, TDPA. CAS No. 4671-75-4. Pack Sizes: 1 g/5 g/100 g. Product ID: tetradecylphosphonic acid. Molecular formula: 278.37 g/mol. Mole weight: C14H31O3P. CCCCCCCCCCCCCCP(=O)(O)O. InChI=1S / C14H31O3P / c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18 (15, 16) 17 / h2-14H2, 1H3, (H2, 15, 16, 17). BVQJQTMSTANITJ-UHFFFAOYSA-N.
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