Methyl myristelaidate

CAT:
952-B2018085
Size:
50 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Methyl myristelaidate - image 1

Methyl myristelaidate

  • Description:

    Methyl myristelaidate_x000D_ Catalog number: B2018085_x000D_ Lot number: Batch Dependent_x000D_ Expiration Date: Batch dependent_x000D_ Amount: 50 mg_x000D_ Molecular Weight or Concentration: 240.38_x000D_ Supplied as: Solution_x000D_ Applications: a molecular tool for various biochemical applications_x000D_ Storage: -20℃_x000D_ Keywords: Methyl trans-9-tetradecenoate, Myristelaidic acid methyl ester_x000D_ Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ References:_x000D_ 1: Wu C, Wang Y, Sun H. Targeted and untargeted metabolomics reveals deep analysis of drought stress responses in needles and roots of Pinus taeda seedlings Front Plant Sci. 2023 Jan 31;13:1031466._x000D_ 2: Doma AO, Cristina RT, Muselin F, Dumitrescu E, Dégi J, Imre K, Boldea M, Vlad DC, Popescu R, Cimporescu A, Bratu DC. The Role of Methyl-(Z)-11-tetradecenoate Acid from the Bacterial Membrane Lipid Composition in Escherichia coli Antibiotic Resistance Biomed Res Int. 2022 Jun 13;2022:6028045._x000D_ 3: Choi MH, Yoon SC. Polyester Biosynthesis Characteristics of Pseudomonas citronellolis Grown on Various Carbon Sources, Including 3-Methyl-Branched Substrates Appl Environ Microbiol. 1994 Sep;60(9):3245-54._x000D_ 4: Watanabe H, Matsui A, Inomata S, Yamamoto M, Ando T. Biosynthetic Pathway for Sex Pheromone Components Produced in a Plusiinae Moth, Plusia festucae Front Endocrinol (Lausanne). 2011 Nov 14;2:74._x000D_ 5: Petkevicius K, Wenning L, Kildegaard KR, Sinkwitz C, Smedegaard R, Holkenbrink C, Borodina I. Biosynthesis of insect sex pheromone precursors via engineered β-oxidation in yeast FEMS Yeast Res. 2022 Sep 1;22(1):foac041._x000D_ 6: Hasan MM, Chowdhory SA, Rahman ASMS, Athanassiou CG. Development and diapause induction of the Indian meal moth, Plodia interpunctella (Hübner) (Lepidoptera: Pyralidae) at different photoperiods Sci Rep. 2020 Sep 7;10(1):14707._x000D_ 7: Ma PW, Roelofs WL. Sex pheromone gland of the female European corn borer moth, Ostrinia nubilalis (Lepidoptera, Pyralidae): ultrastructural and biochemical evidences Zoolog Sci. 2002 May;19(5):501-11._x000D_ 8: Miura Y, Fulco AJ. Omega-1, Omega-2 and Omega-3 hydroxylation of long-chain fatty acids, amides and alcohols by a soluble enzyme system from Bacillus megaterium Biochim Biophys Acta. 1975 Jun 23;388(3):305-17._x000D_ 9: Chao TH, Ehrman L, Permaul A, Vincent R, Sattaur L, Brandt D. Male-specific cuticular compounds of the six Drosophila paulistorum semispecies: structural identification and mating effect J Chem Ecol. 2010 Sep;36(9):933-42._x000D_ 10: Navarro I, Fabriàs G, Camps F. Possible fatty acyl pheromone precursors in Spodoptera littoralis. Search for 11- and 12-hydroxytetradecanoic acids in the pheromone gland Lipids. 1997 Apr;32(4):407-12. _x000D_ _x000D_ Products Related to Methyl myristelaidate can be found at Chemicals
  • Short Description:

    Catalog Number: B2018085 (50 mg)
  • Weight:

    0.15
  • Length:

    2
  • Width:

    0.5
  • Height:

    0.5
  • Height :

    0.5