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Tetramethylrhodamine-5-carboxamide lysine

$695.00

Catalog Number: B2011143 (1 mg)
Tetramethylrhodamine-5-carboxamide lysine is a high quality transglutaminase substrate
. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

In stock

SKU: B2011143 Categories: ,

Description

Tetramethylrhodamine-5-carboxamide lysine
Catalog number: B2011143
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 mg
Molecular Weight or Concentration: 559 g/mol
Supplied as: Lyophilized
Applications: molecular tool for various biochemical applications
Storage: -20 °C
Keywords: 5-TAMRA Lysine
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.

References:
1: Song J, Han Z, Zheng YG. Identification and Profiling of Histone Acetyltransferase Substrates by Bioorthogonal Labeling Curr Protoc. 2022 Jul;2(7):e497.
2: Swyter S, Schiedel M, Monaldi D, Szunyogh S, Lehotzky A, Rumpf T, Ovádi J, Sippl W, Jung M. New chemical tools for probing activity and inhibition of the NAD(+)-dependent lysine deacylase sirtuin 2 Philos Trans R Soc Lond B Biol Sci. 2018 Jun 5;373(1748):20170083.
3: Shah S, Mandecki W, Li J, Gryczynski Z, Borejdo J, Gryczynski I, Fudala R. FRET study in oligopeptide-linked donor-acceptor system in PVA matrix Methods Appl Fluoresc. 2016 Dec 13;4(4):047002.
4: Weiss N, Seneviranthe C, Jiang M, Wang K, Luo M. Profiling and Validation of Live-Cell Protein Methylation with Engineered Enzymes and Methionine Analogues Curr Protoc. 2021 Aug;1(8):e213.
5: Zhu D, Yang RX, Tang YP, Li W, Miao ZY, Hu Y, Chen J, Yu S, Wang J, Xu CY. Robust nanoplasmonic substrates for aptamer macroarrays with single-step detection of PDGF-BB Biosens Bioelectron. 2016 Nov 15;85:429-436.
6: Kuru E, Tekkam S, Hall E, Brun YV, Van Nieuwenhze MS. Synthesis of fluorescent D-amino acids and their use for probing peptidoglycan synthesis and bacterial growth in situ Nat Protoc. 2015 Jan;10(1):33-52.
7: De Marco Almeida F, Silva CN, de Araujo Lopes SC, Santos DM, Torres FS, Cardoso FL, Martinelli PM, da Silva ER, de Lima ME, Miranda LAF, Oliveira MC. Physicochemical Characterization and Skin Permeation of Cationic Transfersomes Containing the Synthetic Peptide PnPP-19 Curr Drug Deliv. 2018;15(7):1064-1071.
8: Fryatt AG, Dayl S, Cullis PM, Schmid R, Evans RJ. Mechanistic insights from resolving ligand-dependent kinetics of conformational changes at ATP-gated P2X1R ion channels Sci Rep. 2016 Sep 12;6:32918.
9: Hanz GM, Jung B, Giesbertz A, Juhasz M, Weinhold E. Sequence-specific labeling of nucleic acids and proteins with methyltransferases and cofactor analogues J Vis Exp. 2014 Nov 22;(93):e52014.
10: Susa K, Sohara E, Rai T, Zeniya M, Mori Y, Mori T, Chiga M, Nomura N, Nishida H, Takahashi D, Isobe K, Inoue Y, Takeishi K, Takeda N, Sasaki S, Uchida S. Impaired degradation of WNK1 and WNK4 kinases causes PHAII in mutant KLHL3 knock-in mice Hum Mol Genet. 2014 Oct 1;23(19):5052-60.

Products Related to Tetramethylrhodamine-5-carboxamide lysine can be found at Chemicals

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