Name: 5(6)-TAMRA cadaverine
Brand: AAT Bioquest
SKU: 355
Price: 348 USD
Availability: InStock

5(6)-TAMRA cadaverine

5(6)-TAMRA cadaverine is a building block for developing fluoresceinated bioconjugates. It is also a fluorescent transglutaminase substrate to label proteins by transaminidation. TAMRA is one of the most popular fluorophores used in various bioconjugations. TMR is a bright orange fluorophore. 5(6)-TAMRA is the mixture of two carboxy tetramethylrhodamine (TMR) isomers.

Protocol

SDS

COA

Catalog	Size	Price	Quantity
355	25 mg	Price

Calculators

Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of 5(6)-TAMRA cadaverine 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	134.651 µL	673.256 µL	1.347 mL	6.733 mL	13.465 mL
5 mM	26.93 µL	134.651 µL	269.302 µL	1.347 mL	2.693 mL
10 mM	13.465 µL	67.326 µL	134.651 µL	673.256 µL	1.347 mL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

Mass (Calculate)		Molecular weight		Volume (Calculate)		Concentration (Calculate)		Moles
mg	÷	742.66 g/mol	=	mL	x	mM	=	mmol

Citations

View all 3 citations: Citation Explorer

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

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

Advances in Quantitative FRET-Based Methods for Studying Nucleic Acids

Authors:

Preus, Søren and Wilhelmsson, L Marcus

Journal:

ChemBioChem (2012): 1990--2001

References

View all 96 references: Citation Explorer

Fluorescence anisotropy and FRET studies of G-quadruplex formation in presence of different cations

Authors:

Juskowiak B, Galezowska E, Zawadzka A, Gluszynska A, Takenaka S.

Journal:

Spectrochim Acta A Mol Biomol Spectrosc (2006): 835

G Quadruplex-Based FRET Probes with the Thrombin-Binding Aptamer (TBA) Sequence Designed for the Efficient Fluorometric Detection of the Potassium Ion

Authors:

Nagatoishi S, Nojima T, Galezowska E, Juskowiak B, Takenaka S.

Journal:

Chembiochem (2006): 1730

A targeted protease substrate for a quantitative determination of protease activities in the endolysosomal pathway

Authors:

Fischer R, Bachle D, Fotin-Mleczek M, Jung G, Kalbacher H, Brock R.

Journal:

Chembiochem (2006): 1428

Electrostatic-gated transport in chemically modified glass nanopore electrodes

Authors:

Wang G, Zhang B, Wayment JR, Harris JM, White HS.

Journal:

J Am Chem Soc (2006): 7679

Metal-enhanced fluorescence-based RNA sensing

Authors:

Aslan K, Huang J, Wilson GM, Geddes CD.

Journal:

J Am Chem Soc (2006): 4206

Physical properties

Molecular weight	742.66
Solvent	DMSO

Spectral properties

Correction factor (260 nm)	0.32
Correction factor (280 nm)	0.178
Extinction coefficient (cm ^-1 M ^-1)	90000
Excitation (nm)	552
Emission (nm)	578

Storage, safety and handling

H-phrase	H303, H313, H333
Hazard symbol	XN
Intended use	Research Use Only (RUO)
R-phrase	R20, R21, R22
Storage	Freeze (< -15 °C); Minimize light exposure
UNSPSC	12171501

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Page updated on October 13, 2025