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| Product | Description | |
|---|---|---|
| Sumiceller | Sumiceller. Group: Polymers. |  |
| Sumifix dark brown brs | Sumifix dark brown brs. Uses: Designed for use in research and industrial production. Additional or Alternative Names: C.I. Reactive Brown 21;Reactive Brown 21;Sumifix Dark Brown BRS. Product Category: Heterocyclic Organic Compound. CAS No. 154999-66-3. Mole weight: 0. Product ID: ACM154999663. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Sumilizer GA 80 | Sumilizer GA 80. Group: Biochemicals. Grades: Highly Purified. CAS No. 90498-90-1. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C43H64O10. US Biological Life Sciences. |  Worldwide |
| Sumipanel | Sumipanel. Group: Polymers. | |
| SUMO-1 human | ?95% (SDS-PAGE), recombinant, expressed in E. coli (GST-tagged). Group: Fluorescence/luminescence spectroscopy. |  |
| SUMO Protease 1 (GST-tagged) from Yeast, Recombinant | SUMO (Small Ubiquitin-like MOdifiers) Protease 1 (Ulp1, Ubl-specific protease 1 from Saccharomyces cerevisiae) is a highly active cysteine protease. It is highly specific as it recognizes the tertiary structure of the ubiquitin-like (UBL) protein, SUMO (Smt3), rather than its amino acid sequence. SUMO fusion tag, as an N-terminal fusion partner, has been shown to enhance functional protein production in prokaryotic and eukaryotic expression systems with significantly improved protein stability and solubility. The SUMO protease 1 can be used to cleave SUMO protein tag from recombinant SUMO-fusion proteins. The optimal temperature for cleavage is 30°C; however, the en...eaction by affinity chromatography using the Glutathione resin. Group: Enzymes. Synonyms: Ulp1 peptidase; SUMO Protease; SUMO Protease. Enzyme Commission Number: EC 3.4.22.68. Purity: > 90% by SDS-PAGE. Mole weight: 52.6 kDa (403-621 aa + N-terminal GST). Activity: >10,000 units/mg. Storage: Store at -80°C. Stable for at least 1 year as supplied. It may be further diluted to 0.1-0.5 mg/ml with 50 mM Tris-HCl, 100 mM NaCl, 5 mM DTT and 20% glycerol pH 8.0 and stored at -20°C in aliquots. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Yeast. Ulp1 peptidase; SUMO Protease; SUMO Protease; SUMO Protease 1; Protease. Cat No: NATE-1708. |  |
| SUMO Protease 1 (His-tagged) from Yeast, Recombinant | SUMO (Small Ubiquitin-like MOdifiers) Protease 1 (Ulp1, Ubl-specific protease 1 from Saccharomyces cerevisiae) is a highly active cysteine protease. It is highly specific as it recognizes the tertiary structure of the ubiquitin-like (UBL) protein, SUMO (Smt3), rather than its amino acid sequence. SUMO fusion tag, as an N-terminal fusion partner, has been shown to enhance functional protein production in prokaryotic and eukaryotic expression systems with significantly improved protein stability and solubility. The SUMO Protease 1 can be used to cleave SUMO protein tag from recombinant SUMO-fusion proteins. The optimal temperature for cleavage is 30°C; however, the en...finity chromatography using the Ni chelating resin. Group: Enzymes. Synonyms: Ulp1 peptidase; SUMO Protease; SUMO Protease. Enzyme Commission Number: EC 3.4.22.68. Purity: > 90% by SDS-PAGE. Mole weight: 28.7 kDa (403-621 aa + N-terminal Poly-His tag). Activity: 1 X 10^6 units/mg. Storage: Store at -80°C. Stable for at least 1 year as supplied. It may be further diluted to 0.01-0.05 mg/ml with 50 mM Tris-HCl, 100 mM NaCl, 5 mM DTT and 20% glycerol pH 8.0 and stored at -20°C in aliquots. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Yeast. Ulp1 peptidase; SUMO Protease; SUMO Protease; SUMO Protease 1; Protease. Cat No: NATE-1709. | |
| SUN | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| SUN 11602 | SUN 11602. Group: Biochemicals. Grades: Purified. CAS No. 704869-38-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| SUN-B 8155 | SUN-B 8155. Group: Biochemicals. Grades: Purified. CAS No. 345893-91-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Sundew Dry Herb Extract 10:1 (Drosera rotundifolia) | Sundew Dry Herb Extract 10:1 (Drosera rotundifolia). |  CA, FL & NJ |
| Sunflower CO2 | Sunflower CO2 (Peanut Replacer). CAS No. 8001-21-6. Kosher: Y. VIGON Item # 507454. Categories: Speciality Ingrdients Suppliers. |  America & Internationally |
| Sunflower oil | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sunflower oil | Sunflower oil occurs as a clear, light yellow-colored liquid with a bland, agreeable taste. Synonyms: Helianthi annui oleum raffinatum; huile de tournesol; oleum helianthi; sunflowerseed oil. CAS No. 8001-21-6. Product ID: PE-0552. Category: Diluent; emollient; Emulsifying Agents; Solvent; Tablet Binder. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0552; Sunflower oil; Diluent; emollient; Emulsifying Agents; Solvent; Tablet Binder; ; 8001-21-6. UNII: NA. Chemical Name: Sunflower oil. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Sunflower oil should be stored in an airtight, well-filled container, protected from light. Stability may be improved by the addition of an antioxidant such as butylated hydroxytoluene. Source and Preparation: Sunflower oil is obtained from the fruits and seeds (achenes) of the sunflower, Helianthus annus (Compositae), by mechanical means or by extraction. Applications: Sunflower oil is widely used as an edible oil, primarily in oleomargarine. It is also used extensively in cosmetics and pharmaceutical formulations. Therapeutically, sunflower oil is used to provide energy and essential fatty acids for parenteral nutrition. Studies have shown that sunflower oil may be used in intramuscular injections without inducing tissue damage. Safety: Sunflower oil is widely used in food products and on its own as an edible oil. It is also used extens |  |
| Sunflower oil | Sunflower oil occurs as a clear, light yellow-colored liquid with a bland, agreeable taste. Synonyms: Helianthi annui oleum raffinatum; huile de tournesol; oleum helianthi; sunflowerseed oil. CAS No. 8001-21-6. Product ID: PE-0473. Category: Binder Excipients. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Sunflower oil; Binder Excipients; Binder Excipients; 8001-21-6; 8001-21-6. UNII: NA. Chemical Name: Sunflower oil. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Sunflower oil should be stored in an airtight, well-filled container, protected from light. Stability may be improved by the addition of an antioxidant such as butylated hydroxytoluene. Source and Preparation: Sunflower oil is obtained from the fruits and seeds (achenes) of the sunflower, Helianthus annus (Compositae), by mechanical means or by extraction. Applications: Sunflower oil is widely used as an edible oil, primarily in oleomargarine. It is also used extensively in cosmetics and pharmaceutical formulations. Therapeutically, sunflower oil is used to provide energy and essential fatty acids for parenteral nutrition. Studies have shown that sunflower oil may be used in intramuscular injections without inducing tissue damage. Safety: Sunflower oil is widely used in food products and on its own as an edible oil. It is also used extensively in cosmetics and topical pharmaceutical formulations, and is g | |
| Sunflower Oil | Sunflower Oil. CAS No. 8001-21-6. Kosher: Y. VIGON Item # 502711. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Sunflower Oil BP/USP | Sunflower Oil BP/USP. CAS No. 8001-21-6. |  |
| Sunflower Oil Powder 50% Load NG | Sunflower Oil Powder 50% Load NG. | CA, FL & NJ |
| Sunflower Phytosterol Ester 97% | Sunflower Phytosterol Ester 97%. | CA, FL & NJ |
| Sunflower seed oil | analytical standard. Group: Flavor and fragrance standards. | |
| Sunflower seed oil microencapsulated powder | Sunflower seed oil microencapsulated powder. Product ID: CDF4-0205. Molecular formula: NA. Category: Unsaturated fatty acid supplement. Product Keywords: Food Ingredients; Nutrients; CDF4-0205; Sunflower seed oil microencapsulated powder; Unsaturated fatty acid supplement. Appearance: White to light yellow powder. Color: White to light yellow. Physical State: powder. Source and Preparation: sunflower. Applications: Dietary supplements, nutritional supplements, cosmetic raw materials, etc. | |
| Sunitinib | Sunitinib (as the malate salt) is the active ingredient in the drug sold under the trade name Sutent. This drug is a small molecule receptor tyrosine kinase inhibitor that has been approved in at least one country for the treatment of patients having gastrointestinal stromal tumors or renal cell carcinomas. Group: Biochemicals. Alternative Names: N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide; SU-11248; Sutent; PHA-290940AD; PNU-290940AD. Grades: Highly Purified. CAS No. 557795-19-4. Pack Sizes: 10mg, 100mg. Molecular Formula: C22H27FN4O2, Molecular Weight: 398.47. US Biological Life Sciences. | Worldwide |
| Sunitinib | Sunitinib (SU 11248) is a multi-targeted receptor tyrosine kinase inhibitor with IC 50 s of 80 nM and 2 nM for VEGFR2 and PDGFRβ , respectively [1]. Sunitinib, an ATP-competitive inhibitor, effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU 11248. CAS No. 557795-19-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-10255A. |  |
| Sunitinib-d10 | Labeled Sunitinib, a multi-kinase inhibitor targeting several receptor tyrosine kinases (RTK). Group: Biochemicals. Grades: Highly Purified. CAS No. 1126721-82-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sunitinib-[d10] | One of the isotopic labelled form of Sunitinib, which is a receptor tyrosine kinases inhibitor. Synonyms: N-[2-(Diethyl-d10)aminoethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide; Sutent-d10; SU-11248-d10. Grade: >95%. CAS No. 1126721-82-1. Molecular formula: C22H17D10FN4O2. Mole weight: 408.47. |  |
| Sunitinib Impurity 6 | Sunitinib Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1691223-83-2. Molecular formula: C22H27FN4O2. Mole weight: 398.48. Catalog: APB1691223832. | |
| Sunitinib Impurity 61 | Sunitinib Impurity 61. Uses: For analytical and research use. Group: Impurity standards. CAS No. 100487-78-3. Molecular formula: C8H6ClN3O. Mole weight: 195.61. Catalog: APB100487783. | |
| Sunitinib Intermediate | 5-Fluoro-2-oxindole is an impurity of Sunitinib, which is an oral, small-molecule, multi-targeted receptor tyrosine kinase (RTK) inhibitor for the treatment of renal cell carcinoma (RCC) and imatinib-resistant gastrointestinal stromal tumor (GIST). Alternative Names: 5-Fluorooxindole. 5-Fluoro-2-oxindole. 5-fluoroindolin-2-one. 5-fluoro-1,3-dihydroindol-2-one. CAS No. 56341-41-4. Product ID: API56341414. Molecular formula: C8H6FNO. Mole weight: 151.14. EINECS: 638-803-9. SMILES: C1C2=C(C=CC(=C2)F)NC1=O. Appearance: Off-white to Beige Solid. Category: Intermediates. |  |
| Sunitinib malate | Sunitinib (marketed as Sutent by Pfizer, and previously known as SU11248) is an oral, small-molecule, multi-targeted receptor tyrosine kinase (RTK) inhibitor that was approved by the FDA for the treatment of renal cell carcinoma (RCC) and imatinib-resistant gastrointestinal stromal tumor (GIST) on January 26, 2006. Sunitinib was the first cancer drug simultaneously approved for two different indications. Uses: Angiogenesis inhibitors. Synonyms: Sunitinib malate; SU011248 L-malate salt; N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide; (2S)-2-hydroxybutanedioic acid. Grade: >98%. CAS No. 341031-54-7. Molecular formula: C22H27FN4O2.C4H6O5. Mole weight: 532.56. | |
| Sunitinib malate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Sunitinib Malate | A multi-kinase inhibitor targeting several receptor tyrosine kinases (RTK). Antineoplastic. Group: Biochemicals. Alternative Names: N-[2-(Diethylamino)ethyl]-5-[(Z)-(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide Malate; Sutent; SU-11248. Grades: Highly Purified. CAS No. 341031-54-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Sunitinib Malate | An indole and pyrrole derivative that inhibits VEGFR-2 and PDGFR BETA RECEPTOR TYROSINE KINASES. It is used as an antineoplastic agent for the treatment of GASTROINTESTINAL STROMAL TUMORS, and for treatment of advanced or metastatic RENAL CELL CARCINOMA. Alternative Names: Sutent. SU011248 L-malate salt. PHA-290940AD. CAS No. 341031-54-7. Product ID: API341031547. Molecular formula: C26H33FN4O7. Mole weight: 532.6. EINECS: 638-825-9. SMILES: CCN(CC)CCNC(=O)C1=C(NC(=C1C)C=C2C3=C(C=CC(=C3)F)NC2=O)C.C(C(C(=O)O)O)C(=O)O. Appearance: Yellow to Orange Solid. Category: Anti-Tumor APIs. | |
| Sunitinib Malate | Sunitinib Malate (SU 11248 Malate) is a multi-targeted receptor tyrosine kinase inhibitor with IC 50 s of 80 nM and 2 nM for VEGFR2 and PDGFRβ , respectively [1]. Sunitinib Malate, an ATP-competitive inhibitor, effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU 11248 Malate. CAS No. 341031-54-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-10255. | |
| Sunitinib Maleate (Sutent, Sunitinib Malate, SU-11248, PHA-290940AD, PNU-290940AD) | A multi-kinase inhibitor targeting several receptor tyrosine kinases (RTK). Sunitinib and its active metabolite (SU012662) are selective inhibitors of multiple receptor tyrosine kinases, including platelet-derived growth factor receptor and vascular endothelial growth factor receptor, that are associated with tumor growth and angiogenesis. Group: Biochemicals. Alternative Names: Sutent. Grades: Highly Purified. CAS No. 341031-54-7. Pack Sizes: 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| Sunitinib N-Oxide | Sunitinib N-Oxide. Group: Biochemicals. Alternative Names: N-[2- (Diethyloxidoamino) ethyl]-5-[ (Z) - (5-fluoro-1, 2-dihydro-2-oxo-3H-indol-3-ylidene) methyl]-2, 4-dimethyl-1H-pyrrole-3-carboxamide; 5-(5-Fluoro-2-oxo-1,2-dihydroindol-(3Z)-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-diethyl-N-oxoaminoethyl)amide. Grades: Highly Purified. CAS No. 356068-99-0. Pack Sizes: 10mg. Molecular Formula: C22H27FN4O3, Molecular Weight: 414.47. US Biological Life Sciences. | Worldwide |
| Sunitinib N-Oxide-d10 | Sunitinib N-Oxide-d10. Group: Biochemicals. Alternative Names: N-[2- (Diethyloxidoamino) ethyl]-5-[ (Z) - (5-fluoro-1, 2-dihydro-2-oxo-3H-indol-3-ylidene) methyl]-2, 4-dimethyl-1H-pyrrole-3-carboxamide-d10; 5-(5-Fluoro-2-oxo-1,2-dihydroindol-(3Z)-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-diethyl-N-oxoaminoethyl)amide-d10. Grades: Highly Purified. Pack Sizes: 500ug. Molecular Formula: C22H17D10FN4O3, Molecular Weight: 424.53. US Biological Life Sciences. | Worldwide |
| Sunply | Sunply. Group: Polymers. | |
| Sunset Yellow FCF | analytical standard. Group: Colorant standards. | |
| Sunset Yellow FCF | Provisionally listed for use in food, drugs and cosmetics. Sunset Yellow is useful in fermented foods which must be heat treated. It may be found in orange sodas, orange jelly, marzipan, Swiss rolls, apricot jam, citrus marmalade, lemon curd, sweets, hot chocolate mix and packet soups, trifle mix, breadcrumbs, snack chips, shelf fresh noodles, cheese sauce mixes. Sunset Yellow is a sulfonated version of Sudan I, a possible carcinogen. Sunset Yellow itself may be responsible for causing an allergic reaction in people with an aspirin intolerance, resulting in various symptoms, including gastric upset, diarrhea, vomiting, nettle rash (urticaria), swelling of the skin (angioedema) and migraines. Group: Biochemicals. Grades: Highly Purified. CAS No. 2783-94-0. Pack Sizes: 1g, 10g. US Biological Life Sciences. | Worldwide |
| Sunset Yellow FCF | Sunset Yellow FCF (Orange Yellow S) is an orange azo dye with a maximum absorption wavelength of 480 nm. Sunset Yellow FCF can be used in food, cosmetics and pharmaceuticals [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: Orange Yellow S; Food Yellow 3; CI 15985. CAS No. 2783-94-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-D0249. | |
| Sunvozertinib | Sunvozertinib, also known as DZD9008, is an oral, potent, irreversible, and selective EGFR tyrosine kinase inhibitor. Sunvozertinib shows activity against EGFRexon20ins and other mutations. In both cell lines and xenograft models, sunvozertinib shows potent antitumor activity. In the two ongoing phase I clinical studies, sunvozertinib was tolerated up to 400 mg once daily. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Sunvozertinib; DZD 9008; (DZD-9008; DZD9008. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 2370013-12-8. Molecular formula: C29H35ClFN7O3. Mole weight: 584.09. Purity: >98%. IUPACName: N-{5-({4-[5-chloro-4-fluoro-2-(2-hydroxypropan-2-yl)anilino]pyrimidin-2-yl}amino)-2-[(3R)-3-(dimethylamino)pyrrolidin-1-yl]-4-methoxyphenyl}prop-2-enamide. Canonical SMILES: C=CC(NC1=CC(NC2=NC=CC(NC3=CC(Cl)=C(F)C=C3C(C)(O)C)=N2)=C(OC)C=C1N4C[C@H](N(C)C)CC4)=O. Product ID: ACM2370013128. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sunvozertinib | Sunvozertinib (DZD9008) is a potent ErbBs (EGFR, Her2, especially mutant forms) and BTK inhibitor. Sunvozertinib shows IC 50 s of 20.4, 20.4, 1.1, 7.5, and 80.4 nM for EGFR exon 20 NPH insertion, EGFR exon 20 ASV insertion, EGFR L858R and T790M mutations, and Her2 Exon20 YVMA, and EGFR WT A431, respectively (patent WO2019149164A1, example 52) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DZD9008. CAS No. 2370013-12-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132842. | |
| SuO-Glu-Val-Cit-PAB-MMAE | SuO-Glu-Val-Cit-PAB-MMAE (NHS-Glutarate-Val-Cit-PAB-MMAE) consists a cleavable ADC linker (SuO-Glu-Val-Cit-PAB) and a potent tubulin inhibitor (MMAE). SuO-Glu-Val-Cit-PAB-MMAE can be used in the synthesis of antibody-drug conjugates (ADCs)[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NHS-Glutarate-Val-Cit-PAB-MMAE. CAS No. 1895916-24-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-130989. | |
| Supaglutide | Supaglutide is a glucagon-like peptide-1 (GLP-1) analog developed for the treatment of type 2 diabetes mellitus (T2DM). Supaglutide was shown to regulate blood glucose and lipid homeostasis in diabetic rhesus monkeys. Synonyms: YN011-301. | |
| Super Absorbent Polymer | Super Absorbent Polymer. Group: Polymers. Product ID: sodium; prop-2-enenitrile. Molecular formula: 75.04g/mol. Mole weight: C3H2NNa. [CH-]=CC#N.[Na+]. InChI=1S/C3H2N.Na/c1-2-3-4;/h1-2H;/q-1;+1. NTOWCTQVNUDKBY-UHFFFAOYSA-N. | |
| Super Activated Carbon Nanoparticles | Super Activated Carbon Nanoparticles. Group: Metal nano dispersion. CAS No. 7440-44-0. Mole weight: C. 99.9 %. | |
| Super Activated Charcoal Nanopowder | Super Activated Charcoal Nanopowder. Group: Metal nano dispersion. CAS No. 7440-44-0. Molecular formula: 12.01 g/mol. Mole weight: C. | |
| Supercinnamaldehyde | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Supercinnamaldehyde | Supercinnamaldehyde is a potent transient receptor potential ankyrin 1 (TRPA1) activator with an EC 50 value of 0.8 μM. Supercinnamaldehyde activates TRPA1 ion channels through covalent modification of cysteines [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 70351-51-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121539. | |
| Superconfluentic acid | Superconfluentic acid is a depside metabolite of the lichen. CAS No. 108529-22-2. Molecular formula: C32H44O8. Mole weight: 556.69. | |
| Super-DHB | suitable for matrix substance for MALDI-MS, ?99.0%. Group: Fluorescence/luminescence spectroscopy. | |
| Superfibronectin from human plasma | solution, sterile-filtered, BioReagent, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Super high polymerization degree floating polyvinyl chloride resin | Super high polymerization degree floating polyvinyl chloride resin. Group: Polymers. | |
| Super large size Nb2CTx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets, the preparation temperature is low, the oxidation is effectively prevented, and the electrochemical and catalytic properties are excellent. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12011-99-3. 0.99. | |
| Super large size Ti2CTx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets. The preparation temperature is low. The oxidation is effectively prevented. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12316-56-2. 0.99. | |
| Super large size Ti3C2Tx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets. The preparation temperature is low. The oxidation is effectively prevented. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12363-89-2. 0.99. | |
| Super large size V2CTx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets, the preparation temperature is low, the oxidation is effectively prevented, and the electrochemical and catalytic properties are excellent. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. 0.99. | |
| superoxide dismutase | A metalloprotein; also known as erythrocuprein, hemocuprein or cytocuprein. Enzymes from most eukaryotes contain both copper and zinc; those from mitochondria and most prokaryotes contain manganese or iron. Group: Enzymes. Synonyms: superoxidase dismutase; copper-zinc superoxide dismutase; Cu-Zn superoxide dismutase; ferrisuperoxide dismutase; superoxide dismutase I; superoxide dismutase II; SOD; Cu,Zn-SOD; Mn-SOD; Fe-SOD; SODF; SODS; SOD-1; SOD-2; SOD-3; SOD-4; hemocuprein; erythrocuprein; cytocuprein; cuprein; hepatocuprein. Enzyme Commission Number: EC 1.15.1.1. CAS No. 9054-89-1. SOD. 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-1063; superoxide dismutase; EC 1.15.1.1; 9054-89-1; superoxidase dismutase; copper-zinc superoxide dismutase; Cu-Zn superoxide dismutase; ferrisuperoxide dismutase; superoxide dismutase I; superoxide dismutase II; SOD; Cu,Zn-SOD; Mn-SOD; Fe-SOD; SODF; SODS; SOD-1; SOD-2; SOD-3; SOD-4; hemocuprein; erythrocuprein; cytocuprein; cuprein; hepatocuprein. Cat No: EXWM-1063. | |
| Superoxide Dismutase 2 from Human, Recombinant | SOD2 is part of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. SOD2 binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in SOD2 gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. SOD2 destroys radicals which are usually produced within the cells and which are toxic to biological systems. Group: Enzymes. Synonyms: Superoxide dismutase [Mn]; mitochondrial; IPOB; MNSOD; MVCD6. Enzyme Commission Number: EC 1.15.1.1. Purity: > 95% by SDS-PAGE. SOD. Mole weight: 24.4 kDa (219 aa, 25-222 aa + His Tag). Activity: > 1,200 units/mg. Storage: Can be stored at 4°C short term (1-2 weeks). For long term storage, aliquot and store at - 20°C or -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Human. Superoxide dismutase [Mn]; mitochondrial; IPOB; MNSOD; MVCD6; Superoxide Dismutase 2; SOD-2; Mn-SOD; Mn Superoxide dismutase. Cat No: NATE-1658. | |
| Superoxide Dismutase 8,000u/g (Bovine) (SOD) | Superoxide Dismutase 8,000u/g (Bovine) (SOD). | CA, FL & NJ |
| Superoxide Dismutase A from Bacterial, Recombinant | Superoxide dismutase, Mn, also known as sodA, is a member of the iron/manganese superoxide dismutase family. SodA destroys radicals which are normally produced within the cells and which are toxic to biological systems. It works by catalyzing the dismutation of the superoxide radical O2- to O2 and H2O2, which are then metabolized to H2O and O2 by catalase and glutathione peroxidase. Group: Enzymes. Enzyme Commission Number: EC 1.15.1.1. Purity: > 95% by SDS-PAGE. SOD. Mole weight: 25.2 kDa (226 aa, 1-206 aa + His Tag). Activity: >350 units/mg. Form: Liquid. Source: E. coli. Species: Bacterial. Cat No: NATE-1659. | |
| Superoxide Dismutase from Bovine, Recombinant | Superoxide dismutase (SOD) catalyzes the dismutation of superoxide radicals to hydrogen peroxide and molecular oxygen. SOD plays a critical role in the defense of cells against the toxic effects of oxygen radicals. SOD competes with nitric oxide (NO) for superoxide anion (which reacts with NO to form peroxynitrite), thereby SOD promotes the activity of NO. SOD has also been shown to suppress apoptosis in cultured rat ovarian follicles, neural cell lines, and transgenic mice by preventing the conversion of NO to peroxynitrate, an inducer of apoptosis. Sod from bovine erythr ocytes was the first sod to be found in mammalian tissues. before its enzymatic activity was disc...Superoxide dismutase has been used in a study to investigate where lipoproteins may affect the l-arginine-nitric oxide pathway. superoxide dismutase has also been used in a study to investigate the mass spectral evidence for carbonate-anion-radical-induced posttranslational modification of tryptophan to kynurenine in human cu, zn superoxide dismutase. the product has been used to develop an sod assay. this assay used dismutase-mediated inhibition of nadh-dependent nitroblue tetrazolium reduction. Group: Enzymes. Synonyms: Superoxide dismutases; EC 1.15.1.1; superoxidase dismutase; copper-zinc superoxide dismutase; Cu-Zn superoxide dismutase; ferrisuperoxide dismutase; s | |
| Superoxide Dismutase from Human, Recombinant | Superoxide dismutase (SOD) catalyzes the dismutation of superoxide radicals to hydrogen peroxide and molecular oxygen. SOD plays a critical role in the defense of cells against the toxic effects of oxygen radicals. SOD competes with nitric oxide (NO) for superoxide anion (which reacts with NO to form peroxynitrite), thereby SOD promotes the activity of NO. SOD has also been shown to suppress apoptosis in cultured rat ovarian follicles, neural cell lines, and transgenic mice by preventing the conversion of NO to peroxynitrate, an inducer of apoptosis. Group: Enzymes. Synonyms: Superoxide dismutase [Cu-Zn]; EC 1.15.1.1; SOD1; SOD; ALS; ALS1; IPOA. Enzyme Commission Number: EC 1.15.1.1. Purity: > 95% by SDS-PAGE. SOD. Mole weight: 16.8 kDa (monomer), 33.6 kDa (homodimer). Activity: ~40,000 U/mg. Storage: Store at -20°C. Form: Lyophilized powder. Source: E. coli. Species: Human. Superoxide dismutase [Cu-Zn]; EC 1.15.1.1; SOD1; SOD; ALS; ALS1; IPOA; Cu-Zn superoxide dismutase; Cu,Zn-SOD. Cat No: NATE-1657. | |
| Superoxide dismutase-polyethylene glycol from bovine erythrocytes | lyophilized powder, ?1,350 units/mg protein. Group: Fluorescence/luminescence spectroscopy. | |
| Superoxide dismutase, Porcine erythrocytes | Superoxide dismutase, Porcine erythrocytes (SOD) is the only antioxidant enzyme that scavenges the superoxide anion by converting this free radical to oxygen and hydrogen peroxide, thus preventing peroxynitrite production and further damage. Superoxide dismutase, Porcine erythrocytes is extensively researched and used in anti-inflammatory, antitumor, radiation protection, and antisenility applications[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SOD. CAS No. 9054-89-1. Pack Sizes: 50 KU; 100 KU. Product ID: HY-129064. | |
| Superoxide Dismutase (SOD) 1IU NBT-mg from Melon | Superoxide Dismutase (SOD) 1IU NBT-mg from Melon. | CA, FL & NJ |
| superoxide reductase | The enzyme contains non-heme iron. Group: Enzymes. Synonyms: neelaredoxin; desulfoferrodoxin. Enzyme Commission Number: EC 1.15.1.2. CAS No. 250679-67-5. 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-1064; superoxide reductase; EC 1.15.1.2; 250679-67-5; neelaredoxin; desulfoferrodoxin. Cat No: EXWM-1064. | |
| Superplanaic acid | Superplanaic acid is a depside obtained from the lichen lecanora planaica. CAS No. 156372-09-7. Molecular formula: C31H44O7. Mole weight: 528.68. | |
| Super Purified Plasma Nanotubes Powder SPT-220 | Super Purified Plasma Nanotubes Powder SPT-220. Uses: Designed for use in research and industrial production. Product Category: Purified Single-wall Carbon Nanotubes. CAS No. 7440-44-0. Product ID: ACM7440440-242. Alfa Chemistry ISO 9001:2015 Certified. | |
| Super Purified Plasma Nanotubes Solution SPT-220 | Super Purified Plasma Nanotubes Solution SPT-220. Uses: Designed for use in research and industrial production. Product Category: Purified Single-wall Carbon Nanotubes. CAS No. 7440-44-0. Product ID: ACM7440440-8. Alfa Chemistry ISO 9001:2015 Certified. | |
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