Ritter Trifluoroiodomethane TMG Reagent

<strong>Ritter Trifluoroiodomethane TMG Reagent</strong>_x000D_ <strong>Catalog number:</strong> B2013031_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 5 mL_x000D_ <strong>Molecular Weight or Concentration:</strong> 311.09 g/mol_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> TMG-CF3I, Tetramethylguanidine-trifluoromethyl iodide adduct_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: Marbach A, Bettenbrock K. lac operon induction in Escherichia coli: Systematic comparison of IPTG and TMG induction and influence of the transacetylase LacA J Biotechnol. 2012 Jan;157(1):82-8._x000D_ 2: Smeland S, Bielack SS, Whelan J, Bernstein M, Hogendoorn P, Krailo MD, Gorlick R, Janeway KA, Ingleby FC, Anninga J, Antal I, Arndt C, Brown KLB, Butterfass-Bahloul T, Calaminus G, Capra M, Dhooge C, Eriksson M, Flanagan AM, Friedel G, Gebhardt MC, Gelderblom H, Goldsby R, Grier HE, Grimer R, Hawkins DS, Hecker-Nolting S, Sundby Hall K, Isakoff MS, Jovic G, Kühne T, Kager L, von Kalle T, Kabickova E, Lang S, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Mayer-Steinacker R, Meyers PA, Nagarajan R, Randall RL, Reichardt P, Renard M, Rechnitzer C, Schwartz CL, Strauss S, Teot L, Timmermann B, Sydes MR, Marina N. Survival and prognosis with osteosarcoma: outcomes in more than 2000 patients in the EURAMOS-1 (European and American Osteosarcoma Study) cohort Eur J Cancer. 2019 Mar;109:36-50._x000D_ 3: Sekine M, Kadokura M, Satoh T, Seio K, Wada T, Fischer U, Sumpter V, Lührmann R. Chemical Synthesis of a 5'-Terminal TMG-Capped Triribonucleotide m(3)(2,2,7)G(5)(')pppAmpUmpA of U1 RNA J Org Chem. 1996 Jun 26;61(13):4412-4422._x000D_ 4: Ebrahimi M, Hosseinkhani S, Heydari A, Khavari-Nejad RA, Akbari J. Improvement of thermostability and activity of firefly luciferase through [TMG][Ac] ionic liquid mediator Appl Biochem Biotechnol. 2012 Oct;168(3):604-15._x000D_ 5: Zhang Z, Lundeen SG, Zhu Y, Carver JM, Winneker RC. In vitro characterization of trimegestone: a new potent and selective progestin Steroids. 2000 Oct-Nov;65(10-11):637-43._x000D_ 6: Khajeh MA, Dehghan G, Dastmalchi S, Shaghaghi M, Iranshahi M. Spectroscopic profiling and computational study of the binding of tschimgine: A natural monoterpene derivative, with calf thymus DNA Spectrochim Acta A Mol Biomol Spectrosc. 2018 Mar 5;192:384-392._x000D_ 7: Ebrahimi M, Hosseinkhani S, Heydari A, Khavari-Nejad RA, Akbari J. Controversial effect of two methylguanidine-based ionic liquids on firefly luciferase Photochem Photobiol Sci. 2012 May;11(5):828-34._x000D_ 8: Zhang X, Chen X, Zhang Y, Liu K, Shen H, Zheng E, Huang X, Hou S, Ma X. A near-infrared fluorescent probe for the ratiometric detection and living cell imaging of β-galactosidase Anal Bioanal Chem. 2019 Dec;411(30):7957-7966._x000D_ 9: Yedavalli VS, Jeang KT. Trimethylguanosine capping selectively promotes expression of Rev-dependent HIV-1 RNAs Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14787-92._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/34776346">10: Ishii Y, Aoki K, Oda M, Ichikawa M, Moriuchi R, Konishi H, Nagashima M, Sadamasu K, Sugishita Y. A study of quality assessment in SARS-CoV-2 pathogen nucleic acid amplification tests performance; from the results of external quality assessment survey of clinical laboratories in the Tokyo Metropolitan Government external quality assessment program in 2020 J Infect Chemother. 2022 Feb;28(2):242-247. </a>_x000D_ _x000D_ <strong>Products Related to Ritter Trifluoroiodomethane TMG Reagent can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>