Tunicamycin from Streptomyces sp

<strong>Tunicamycin from Streptomyces sp</strong>_x000D_ <strong>Catalog number:</strong> B2013622_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 4.90 - 5.10 mg/ml_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> Tunicamycin_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Zhang S, Gui C, Shao M, Kumar PS, Huang H, Ju J. Antimicrobial tunicamycin derivatives from the deep sea-derived Streptomyces xinghaiensis SCSIO S15077 Nat Prod Res. 2020 Jun;34(11):1499-1504._x000D_ 2: Yamamoto K, Ichikawa S. Tunicamycin: chemical synthesis and biosynthesis J Antibiot (Tokyo). 2019 Dec;72(12):924-933._x000D_ 3: Widdick D, Royer SF, Wang H, Vior NM, Gomez-Escribano JP, Davis BG, Bibb MJ. Analysis of the Tunicamycin Biosynthetic Gene Cluster of Streptomyces chartreusis Reveals New Insights into Tunicamycin Production and Immunity Antimicrob Agents Chemother. 2018 Jul 27;62(8):e00130-18._x000D_ 4: Yu Y, Tang B, Dai R, Zhang B, Chen L, Yang H, Zhao G, Ding X. Identification of the streptothricin and tunicamycin biosynthetic gene clusters by genome mining in Streptomyces sp. strain fd1-xmd Appl Microbiol Biotechnol. 2018 Mar;102(6):2621-2633._x000D_ 5: Liras P, Marta JF. Streptomyces clavuligerus: The Omics Era J Ind Microbiol Biotechnol. 2021 Dec 23;48(9-10):kuab072._x000D_ 6: Tsvetanova BC, Kiemle DJ, Price NP. Biosynthesis of tunicamycin and metabolic origin of the 11-carbon dialdose sugar, tunicamine J Biol Chem. 2002 Sep 20;277(38):35289-96._x000D_ 7: Sechler AJ, Tancos MA, Schneider DJ, King JG, Fennessey CM, Schroeder BK, Murray TD, Luster DG, Schneider WL, Rogers EE. Whole genome sequence of two Rathayibacter toxicus strains reveals a tunicamycin biosynthetic cluster similar to Streptomyces chartreusis PLoS One. 2017 Aug 10;12(8):e0183005._x000D_ 8: Han EJ, Lee SR, Hoshino S, Seyedsayamdost MR. Targeted Discovery of Cryptic Metabolites with Antiproliferative Activity ACS Chem Biol. 2022 Nov 18;17(11):3121-3130._x000D_ 9: Price NP, Tsvetanova B. Biosynthesis of the tunicamycins: a review J Antibiot (Tokyo). 2007 Aug;60(8):485-91._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/31582803">10: Kimura KI. Liposidomycin, the first reported nucleoside antibiotic inhibitor of peptidoglycan biosynthesis translocase I: The discovery of liposidomycin and related compounds with a perspective on their application to new antibiotics J Antibiot (Tokyo). 2019 Dec;72(12):877-889. </a>_x000D_ _x000D_ <strong>Products Related to Tunicamycin from Streptomyces sp can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>