5-TAMRA, SE (5-Carboxitetrametilrodamina, succinimidilo éster), isómero único
5-TAMRA, SE (5-Carboxitetrametilrodamina, succinimidilo éster), isómero único
Invitrogen™

5-TAMRA, SE (5-Carboxitetrametilrodamina, succinimidilo éster), isómero único

El 5-TAMRA, SE aminorreactivo y sus conjugados producen fluorescencia roja-anaranjada brillante, insensible al pH (excitación/emisión aproximada máxima ∼546/579) con buenaMás información
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Número de catálogoCantidad
C22115 mg
Número de catálogo C2211
Precio (MXN)
-
Cantidad:
5 mg
El 5-TAMRA, SE aminorreactivo y sus conjugados producen fluorescencia roja-anaranjada brillante, insensible al pH (excitación/emisión aproximada máxima ∼546/579) con buena fotoestabilidad.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Reactividad químicaAmina
Emisión579
Excitación546
Etiqueta o tinteIsómeros TAMRA™, TMR (tetrametilrodamina)
Tipo de producto5-TAMRA SE
Cantidad5 mg
Fracción reactivaEster activo, succinimidilo éster
Condiciones de envíoTemperatura ambiente
Tipo de etiquetaColorantes clásicos
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de – 5 a – 30 °C) y proteger de la luz.

Citations & References (238)

Citations & References
Abstract
Multiplex detection of single-nucleotide variations using molecular beacons.
Authors:Marras SA,Kramer FR,Tyagi S
Journal:Genetic analysis : biomolecular engineering
PubMed ID:10084107
Quantitative polymerase chain reaction-based homogeneous assay with fluorogenic probes to measure c-erbB-2 oncogene amplification.
Authors:Gelmini S, Orlando C, Sestini R, Vona G, Pinzani P, Ruocco L, Pazzagli M
Journal:Clin Chem
PubMed ID:9166227
We describe a PCR-based assay for determining c-erbB-2 oncogene amplification in breast cancer in which we use the TaqMan system. Two fluorogenic probes anneal to the target between primers for c-erbB-2 and beta-globin genes and contain both a reporter dye (6-carboxy-fluorescein) and a quencher dye (6-carboxy-tetramethyl-rhodamine). During the extension phase ... More
DNA sequencing with dye-labeled terminators and T7 DNA polymerase: effect of dyes and dNTPs on incorporation of dye-terminators and probability analysis of termination fragments.
Authors:Lee LG, Connell CR, Woo SL, Cheng RD, McArdle BF, Fuller CW, Halloran ND, Wilson RK
Journal:Nucleic Acids Res
PubMed ID:1598205
The incorporation of fluorescently labeled dideoxynucleotides by T7 DNA polymerase is optimized by the use of Mn2+, fluorescein analogs and four 2'-deoxyribonucleoside 5'-O-(1-thiotriphosphates) (dNTP alpha S's). The one-tube extension protocol was tested on single-stranded templates, as well as PCR fragments which were made single-stranded by digestion with T7 gene 6 ... More
Fluorescence resonance energy transfer analysis of the structure of the four-way DNA junction.
Authors:Clegg RM, Murchie AI, Zechel A, Carlberg C, Diekmann S, Lilley DM
Journal:Biochemistry
PubMed ID:1591245
We have carried out fluorescence resonance energy transfer (FRET) measurements on four-way DNA junctions in order to analyze the global structure and its dependence on the concentration of several types of ions. A knowledge of the structure and its sensitivity to the solution environment is important for a full understanding ... More
A novel fluorescent toxin to detect and investigate Kv1.3 channel up-regulation in chronically activated T lymphocytes.
Authors:Beeton C, Wulff H, Singh S, Botsko S, Crossley G, Gutman GA, Cahalan MD, Pennington M, Chandy KG
Journal:J Biol Chem
PubMed ID:12511563
T lymphocytes with unusually high expression of the voltage-gated Kv1.3 channel (Kv1.3(high) cells) have been implicated in the pathogenesis of experimental autoimmune encephalomyelitis, an animal model for multiple sclerosis. We have developed a fluoresceinated analog of ShK (ShK-F6CA), the most potent known inhibitor of Kv1.3, for detection of Kv1.3(high) cells ... More