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| Product | Description | |
|---|---|---|
| trans-aconitate 2-methyltransferase | Also catalyses the formation of the methyl monoester of cis-aconitate, isocitrate and citrate, but more slowly. While the enzyme from Escherichia coli forms (E)-3-(methoxycarbonyl)-pent-2-enedioate as the product, that from Saccharomyces cerevisiae forms (E)-2-(methoxycarbonylmethyl)butenedioate and is therefore classified as a separate enzyme (cf. EC 2.1.1.145, trans-aconitate 3-methyltransferase). Group: Enzymes. Enzyme Commission Number: EC 2.1.1.144. CAS No. 235107-12-7. 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-1740; trans-aconitate 2-methyltransferase; EC 2.1.1.144; 235107-12-7. Cat No: EXWM-1740. |  |
| trans-aconitate 3-methyltransferase | Also catalyses the formation of the methyl monoester of cis-aconitate, isocitrate and citrate, but more slowly. While the enzyme from Saccharomyces cerevisiae forms (E)-2-(methoxycarbonylmethyl)butenedioate as the product, that from Escherichia coli forms (E)-3-(methoxycarbonyl)-pent-2-enedioate and is therefore classified as a separate enzyme (cf. EC 2.1.1.144, trans-aconitate 2-methyltransferase). Group: Enzymes. Enzyme Commission Number: EC 2.1.1.145. CAS No. 235107-12-7. 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-1741; trans-aconitate 3-methyltransferase; EC 2.1.1.145; 235107-12-7. Cat No: EXWM-1741. | |
| Native Porcine Aconitase | Aconitase catalyses the stereo-specific isomerization of Citrate to Isocitrate via cis-aconitate in the tricarboxylic acid cycle. Aconitase is inhibited by cyanide, sulfide and copper and mercury at low concentRations. It is competitively inhibited by trans-aconitate. Aconitase contains an internal Fe-S cluster which is responsible for its activity. Crude preparation containing aconitase activity. Applications: Aconitase may be usefull in diabetes research as well as to study structural conservation between iron-responsive element binding proteins (ire-bp) and isomerases. Group: Enzymes. Synonyms: cis-aconitase; aconitase; Citrate hydro-lyase; Citrate (Isocitrate) hydro-lyase; EC 4.2.1.3; 9024-25-3; aconitate hydRatase. Enzyme Commission Number: EC 4.2.1.3. CAS No. 9024-25-3. Aconitase. Storage: -20°C. Source: Porcine heart. Species: Porcine. cis-aconitase; aconitase; Citrate hydro-lyase; Citrate (Isocitrate) hydro-lyase; EC 4.2.1.3; 9024-25-3; aconitate hydRatase. Cat No: NATE-0024. | |
| trans-Aconitic acid | trans-Aconitic acid is present in normal human urine, and it has been suggested that is present in larger amounts with Reye's syndrome and organic aciduria. trans-Aconitic acid is a substrate of enzyme trans-aconitate 2-methyltransferase. Uses: Scientific research. Group: Natural products. CAS No. 4023-65-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W016813. |  |
| Trimethyl (E)-Aconitate | Protected trans-Aconitic Acid. Group: Biochemicals. Alternative Names: (1E)-1-Propene-1,2,3-tricarboxylic Acid 1,2,3-Trimethyl Ester; Trimethyl trans-Aconitate; trans-Aconitic Acid Trimethyl Ester. Grades: Highly Purified. CAS No. 4271-99-2. Pack Sizes: 500mg. US Biological Life Sciences. |  Worldwide |
| trans-Aconitic acid | 25g Pack Size. Group: Aroma Chemicals, Building Blocks, Organics. Formula: C6H6O6. CAS No. 4023-65-8. Prepack ID 16739536-25g. Molecular Weight 174.11. See USA prepack pricing. |  |
| trans-Aconitic Acid | trans-Aconitic Acid. Group: Biochemicals. Alternative Names: (1E)-1-Propene-1,2,3-tricarboxylic Acid; (E)-Aconitic Acid; trans-1-Propene-1,2,3-tricarboxylic Acid. Grades: Highly Purified. CAS No. 4023-65-8. Pack Sizes: 5g. Molecular Formula: C6H6O6, Molecular Weight: 174.11. US Biological Life Sciences. | Worldwide |
| Trans-Aconitic Acid | Solid;Solid;colourless or yellow crystals, leaves, or plates; pleasant winey acid taste; almost odourless. Group: Monomers. Alternative Names: Achilleic acid. CAS No. 4023-65-8. Product ID: (E)-Prop-1-ene-1,2,3-tricarboxylic acid. Molecular formula: 174.11. Mole weight: C6H6O6. C(C(=CC(=O)O)C(=O)O)C(=O)O. InChI=1S/C6H6O6/c7-4 (8)1-3 (6 (11)12)2-5 (9)10/h1H, 2H2, (H, 7, 8) (H, 9, 10) (H, 11, 12)/b3-1+. GTZCVFVGUGFEME-HNQUOIGGSA-N. 98%. |  |
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