5(6)-TAMRA ethylenediamine
5(6)-TAMRA ethylenediamine is a building block for developing TAMRA bioconjugates. TAMRA is one of the most popular bright orange fluorophores used in various bioconjugations. 5(6)-TAMRA is the mixture of two carboxy tetramethylrhodamine (TMR) isomers.
Calculators
Common stock solution preparation
Table 1. Volume of DMSO needed to reconstitute specific mass of 5(6)-TAMRA ethylenediamine to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.
0.1 mg | 0.5 mg | 1 mg | 5 mg | 10 mg | |
1 mM | 142.739 µL | 713.694 µL | 1.427 mL | 7.137 mL | 14.274 mL |
5 mM | 28.548 µL | 142.739 µL | 285.478 µL | 1.427 mL | 2.855 mL |
10 mM | 14.274 µL | 71.369 µL | 142.739 µL | 713.694 µL | 1.427 mL |
Molarity calculator
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Spectrum
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Product family
Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) | Correction Factor (260 nm) | Correction Factor (280 nm) |
5(6)-FAM ethylenediamine | 493 | 517 | 83000 | 0.32 | 0.178 |
5(6)-TAMRA cadaverine | 552 | 578 | 90000 | 0.32 | 0.178 |
5(6)-TAMRA, SE [5-(and-6)-Carboxytetramethylrhodamine, succinimidyl ester] *CAS 246256-50-8* | 552 | 578 | 90000 | 0.32 | 0.178 |
5(6)-TAMRA Maleimide [Tetramethylrhodamine-5-(and-6)-maleimide] *Mixed isomers* | 552 | 578 | 90000 | 0.32 | 0.178 |
Citations
View all 4 citations: Citation Explorer
Quick-Responsive Polymer-Based Thermo-Sensitive Liposomes for Controlled Doxorubicin Release and Chemotherapy
Authors: Mo, Yulin and Du, Hongliang and Chen, Binlong and Liu, Dechun and Yin, Qingqing and Yan, Yue and Wang, Zenghui and Wan, Fangjie and Qi, Tong and Wang, Yaoqi and others, undefined
Journal: ACS Biomaterials Science & Engineering (2019)
Authors: Mo, Yulin and Du, Hongliang and Chen, Binlong and Liu, Dechun and Yin, Qingqing and Yan, Yue and Wang, Zenghui and Wan, Fangjie and Qi, Tong and Wang, Yaoqi and others, undefined
Journal: ACS Biomaterials Science & Engineering (2019)
Design and Characterization of Two Bifunctional Cryptophane A-Based Host Molecules for Xenon Magnetic Resonance Imaging Applications
Authors: Rossella, Federica and Rose, Honor May and Witte, Christopher and Jayapaul, Jabadurai and Schröder, Leif
Journal: ChemPlusChem (2014): 1463--1471
Authors: Rossella, Federica and Rose, Honor May and Witte, Christopher and Jayapaul, Jabadurai and Schröder, Leif
Journal: ChemPlusChem (2014): 1463--1471
Human erythrocytes as drug carriers: loading efficiency and side effects of hypotonic dialysis, chlorpromazine treatment and fusion with liposomes
Authors: Favretto, ME and Cluitmans, JCA and Bosman, GJCGM and Brock, R
Journal: Journal of Controlled Release (2013): 343--351
Authors: Favretto, ME and Cluitmans, JCA and Bosman, GJCGM and Brock, R
Journal: Journal of Controlled Release (2013): 343--351
Advances in Quantitative FRET-Based Methods for Studying Nucleic Acids
Authors: Preus, Søren and Wilhelmsson, L Marcus
Journal: ChemBioChem (2012): 1990--2001
Authors: Preus, Søren and Wilhelmsson, L Marcus
Journal: ChemBioChem (2012): 1990--2001
References
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