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55222

Sigma-Aldrich

6-Carboxytetramethylrhodamine

BioReagent, suitable for fluorescence, ≥90% (HPLC)

Sinonimo/i:

6-TAMRA

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About This Item

Formula empirica (notazione di Hill):
C25H22N2O5
Numero CAS:
91809-67-5
Peso molecolare:
430.45
Numero MDL:
MFCD00467559
Codice UNSPSC:
12352200
ID PubChem:
57651519
NACRES:
NA.32

Descrizione

single isomer

Nome Commerciale

BioReagent

Saggio

≥90% (HPLC)

Forma fisica

solid

Solubilità

DMSO: soluble
methanol: soluble

Fluorescenza

λex 543 nm; λem 575 nm in 0.1 M Tris pH 8.0

Compatibilità

suitable for fluorescence

Stringa SMILE

CN(C)c1ccc2c(OC3=C\C(C=CC3=C2c4cc(ccc4C([O-])=O)C(O)=O)=[N+](\C)C)c1

InChI

1S/C25H22N2O5/c1-26(2)15-6-9-18-21(12-15)32-22-13-16(27(3)4)7-10-19(22)23(18)20-11-14(24(28)29)5-8-17(20)25(30)31/h5-13H,1-4H3,(H-,28,29,30,31)
COCMHKNAGZHBDZ-UHFFFAOYSA-N

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Applicazioni

6-Carboxytetramethylrhodamine (6-TAMRA) is used to create fluorescent DNA probes and labeled proteins/peptides. The corresponding succinimidyl ester is a single isomer fluorophore most commonly used in automated DNA sequencing.
The corresponding succinimidyl ester is a single isomer fluorophore most commonly used in automated DNA sequencing.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Kevin J Landmark et al.
ACS nano, 2(4), 773-783 (2009-02-12)
Organic-coated superparamagnetic iron oxide nanoparticles (OC-SPIONs) were synthesized and characterized by transmission electron microscopy and X-ray photoelectron spectroscopy. OC-SPIONs were transferred from organic media into water using poly(amidoamine) dendrimers modified with 6-TAMRA fluorescent dye and folic acid molecules. The saturation
Miguel Tavares Pereira et al.
Frontiers in veterinary science, 7, 625921-625921 (2021-02-27)
In the dog, implantation takes place at approximately 17 days of embryonal life and, while exposed to relatively high circulating progesterone concentrations, embryos presence is required for the formation of decidua. Furthermore, a balance between pro- and anti-inflammatory responses in
Redouane Bouchaala et al.
Colloids and surfaces. B, Biointerfaces, 156, 414-421 (2017-05-30)
Light is an attractive trigger for release of active molecules from nanocarriers in biological systems. Here, we describe a phenomenon of light-induced release of a fluorescent dye from lipid nano-droplets under visible light conditions. Using auto-emulsification process we prepared nanoemulsion
Yutaka Ueno et al.
Micromachines, 11(9) (2020-09-16)
This study introduces a modeling method for a supermolecular structure of microtubules for the development of a force generation material using motor proteins. 3D imaging by confocal laser scanning microscopy (CLSM) was used to obtain 3D volume density data. The
Patrick A Marcotte et al.
Analytical biochemistry, 332(1), 90-99 (2004-08-11)
A novel fluorescent substrate was devised for the sirtuin (SIRT) class of human protein deacetylases comprised of a peptide sequence containing a single acetyl-lysine residue, with a fluorescent group (tetramethylrhodamine-6-carboxylic acid, 6-TAMRA) near the carboxyl terminus and a nonfluorescent quenching
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