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5-Carboxytetramethylrhodamine Azide (5-TAMRA-Azide), 10 mg

From  baseclick
≥95 %
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5-((3-Azidopropyl)carbamoyl)-2-(6-(dimethylamino)-3-(dimethyliminio)-3H-xanthen-9-yl)benzoate, 5-TAMRA-Azide
Empirical formula C28H28N6O4
Molar mass (M) 512,56 g/mol
Storage temp. -20 °C
Transport temp. cooled
WGK 1
CAS No. 1192590-89-8

TAMRA fluorescent dye to label DNA/RNA via click chemistry
5-Carboxytetramethylrhodamine Azide (5-TAMRA-Azide) is a reporter reagent that allows efficient fluorescent labeling of nucleic acids by click bioconjugation. It is often used as FRET-acceptor in combination with FAM. Just like many rhodamine-based dyes, it is quite photostable between pH 4 and 9. It shows identical spectral properties to Alexa Fluor® 555 or DyLight 549 dyes.

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Art. No. 7807.3

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5-Carboxytetramethylrhodamine Azide (5-TAMRA-Azide) ≥95 %

Technical Information
Emissions maximum 579 nm 
Instructions for use, addition For a 10 mM solution: add 195 µl to 1 mg. 
5-Carboxytetramethylrhodamine Azide (5-TAMRA-Azide)
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7807.2 5 mg plastic

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7807.3 10 mg plastic

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Downloads / MSDS

General information

Tip:

Consumer Notice:

aqueous media: copper(II) sulfate 7816, sodium ascorbate 7819, THPTA 7822organic solvents (e.g. DMSO): Copper(I) bromide 7813, TBTA 7814 (copper stabilizing ligand)


Reagents for Click Chemistry

Starting from diverse copper catalyst sources, over Cu(I) stabilising ligands to buffer additives and solvents, you will find all necessary reagents in the special ROTI®Click quality to perform your click reactions here.


Click Chemistry

The copper(I)-catalysed azide-alkyne cycloaddition (CuAAC) is the most prominent example of a group of reactions named click reactions. According to Sharpless’ definition, these reactions are characterised by high yields, mild reaction conditions, and by their tolerance of a broad range of functional groups.[1-3] Typically, the reactions require simple or no workup or purification of the product. The most important characteristic of the CuAAC reaction is its unique bioorthogonality as neither azide nor terminal alkyne functional groups are generally present in natural systems.


References:
1 H. C. Kolb, M.G. Finn, K. B. Sharpless, Angew. Chem. Int. Ed. 2001, 40, 2004-2021.
2 C.W. Tornoe, C. Christensen, M. Meldal, J. Org. Chem. 2002, 67, 3057-3064.
3 V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. 2002, 114, 2708-2711; Angew. Chem. Int. Ed. 2002, 41, 2596-2599.


Click Chemistry

In recent years, click chemistry has become increasingly important and steadily more popular in research and development. The reasons for this are not only the easy handling and the high yields but also the countless application possibilities. Carl ROTH offers you the possibility to purchase the broad portfolio of click reagents, various kits for EdU-based cell proliferation assays and numerous other applications from the well-known brand baseclick. This enables us to offer you a necessary and comprehensive assortment for click chemistry.


Certificates of Analysis

You can search for and download your certificate of analysis for the selected product here. Please provide your batch number.
The following analysis certificates have been found:

Type analysis

Appearancepink to dark red colored powder
Assay (LCMS)≥95 %