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6-Carboxytetramethylrhodamine (6-TAMRA)

$595.00

Catalog Number: B2011250 (5 mg)
6-Carboxytetramethylrhodamine (6-TAMRA) is a high quality single isomer of 5(6)-TAMRA used for nucleotide labeling. 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.

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SKU: B2011250 Categories: ,

Description

6-Carboxytetramethylrhodamine (6-TAMRA)
Catalog number: B2011250
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 5 mg
Molecular Weight or Concentration: 430.4 g/mol
Supplied as: Lyophilized
Applications: molecular tool for various biochemical applications
Storage: -20 °C
Keywords: 6-Carboxytetramethylrhodamine
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: Kvach MV, Stepanova IA, Prokhorenko IA, Stupak AP, Bolibrukh DA, Korshun VA, Shmanai VV. Practical synthesis of isomerically pure 5- and 6-carboxytetramethylrhodamines, useful dyes for DNA probes Bioconjug Chem. 2009 Aug 19;20(8):1673-82.
2: Kelemen BR, Klink TA, Behlke MA, Eubanks SR, Leland PA, Raines RT. Hypersensitive substrate for ribonucleases Nucleic Acids Res. 1999 Sep 15;27(18):3696-701.
3: Kelemen BR, Schultz LW, Sweeney RY, Raines RT. Excavating an active site: the nucleobase specificity of ribonuclease A Biochemistry. 2000 Nov 28;39(47):14487-94.
4: Fernandes MM, Gomes AC, Vasconcelos A, Munteanu FD, Tzanov T, Gonçalves MS, End N, Schoening KU, Guebitz GM, Cavaco-Paulo A. Protein disulphide isomerase-assisted functionalization of keratin-based matrices Appl Microbiol Biotechnol. 2011 May;90(4):1311-21.
5: Fujimura S, Ito Y, Ikeguchi M, Adachi K, Yajima J, Nishizaka T. Dissection of the angle of single fluorophore attached to the nucleotide in corkscrewing microtubules Biochem Biophys Res Commun. 2017 Apr 8;485(3):614-620.
6: Jiang M, Tang D, Zhao X, Li Q, Zhuang Y, Wei X, Li X, Liu Y, Wu XY, Shao Z, Gong B, Shen YM. Design and synthesis of new acid cleavable linkers for DNA sequencing by synthesis Nucleosides Nucleotides Nucleic Acids. 2014;33(12):774-85.
7: 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.
8: Landmark KJ, Dimaggio S, Ward J, Kelly C, Vogt S, Hong S, Kotlyar A, Myc A, Thomas TP, Penner-Hahn JE, Baker JR, Holl MM, Orr BG. Synthesis, characterization, and in vitro testing of superparamagnetic iron oxide nanoparticles targeted using folic Acid-conjugated dendrimers ACS Nano. 2008 Apr;2(4):773-83.
9: Takenaka S, Ueyama H, Nojima T, Takagi M. Comparison of potassium ion preference of potassium-sensing oligonucleotides, PSO-1 and PSO-2, carrying the human and Oxytricha telomeric sequence, respectively Anal Bioanal Chem. 2003 Apr;375(8):1006-10.
10: Brandis JW. Dye structure affects Taq DNA polymerase terminator selectivity Nucleic Acids Res. 1999 Apr 15;27(8):1912-8.

Products Related to 6-Carboxytetramethylrhodamine (6-TAMRA) can be found at Fluorescence

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