Alexa Fluor™ 647-aha-dUTP, 1 mM in TE buffer
Alexa Fluor™ 647-aha-dUTP, 1 mM in TE buffer
Invitrogen™

Alexa Fluor™ 647-aha-dUTP, 1 mM in TE buffer

Los nucleótidos marcados 5-aminohexilacrilamido-dUTP (aha-dUTP) se modifican en la posición C-5 de la uridina con un único enlace de hexilacrilamida,Más información
Have Questions?
Número de catálogoCantidad
A3276350 μl
Número de catálogo A32763
Precio (MXN)
-
Cantidad:
50 μl
Los nucleótidos marcados 5-aminohexilacrilamido-dUTP (aha-dUTP) se modifican en la posición C-5 de la uridina con un único enlace de hexilacrilamida, que sirve como separador entre el nucleótido y el tinte. Este espaciador reduce las interacciones entre el nucleótido y el tinte, lo que da como resultado conjugados más brillantes y mayor accesibilidad al hapteno para los reactivos de detección secundarios. Los nucleótidos marcados pueden usarse para generar sondas de hibridación de ácidos nucleicos etiquetados para muchas aplicaciones de biología molecular y citogenética molecular, incluyendo técnicas multicolores.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Concentración1 mM
Para utilizar con (aplicación)Biología molecular
Etiqueta o tinteColorante Alexa Fluor
ModificaciónAHA (5-aminohexilacrilamido)
Línea de productosAlexa Fluor
Tipo de productoNucleótido etiquetado
Cantidad50 μl
Condiciones de envíoHielo húmedo
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de -5 a -30 °C) y proteger de la luz.

Preguntas frecuentes

Can dU-containing DNA produced by amplification with dUTP be cut by restriction enzymes?

You will need to confirm with the manufacturer of the restriction enzyme you are using to find out whether or not it can recognize dUTP-containing DNA.

Find additional tips, troubleshooting help, and resources within our PCR and cDNA Synthesis Support Center.

Citations & References (7)

Citations & References
Abstract
A single-molecule barcoding system using nanoslits for DNA analysis.
Authors:Jo K, Dhingra DM, Odijk T, de Pablo JJ, Graham MD, Runnheim R, Forrest D, Schwartz DC
Journal:Proc Natl Acad Sci U S A
PubMed ID:17296933
'Molecular confinement offers new routes for arraying large DNA molecules, enabling single-molecule schemes aimed at the acquisition of sequence information. Such schemes can rapidly advance to become platforms capable of genome analysis if elements of a nascent system can be integrated at an early stage of development. Integrated strategies are ... More
VHL inactivation is an important pathway for the development of malignant sporadic pancreatic endocrine tumors.
Authors:Schmitt AM, Schmid S, Rudolph T, Anlauf M, Prinz C, Klöppel G, Moch H, Heitz PU, Komminoth P, Perren A,
Journal:Endocr Relat Cancer
PubMed ID:19690016
'A small subset of familial pancreatic endocrine tumors (PET) arises in patients with von Hippel-Lindau syndrome and these tumors may have an adverse outcome compared to other familial PET. Sporadic PET rarely harbors somatic VHL mutations, but the chromosomal location of the VHL gene is frequently deleted in sporadic PET. ... More
Transcriptome for photobiological hydrogen production induced by sulfur deprivation in the green alga Chlamydomonas reinhardtii.
Authors:Nguyen AV, Thomas-Hall SR, Malnoë A, Timmins M, Mussgnug JH, Rupprecht J, Kruse O, Hankamer B, Schenk PM,
Journal:Eukaryot Cell
PubMed ID:18708561
'Photobiological hydrogen production using microalgae is being developed into a promising clean fuel stream for the future. In this study, microarray analyses were used to obtain global expression profiles of mRNA abundance in the green alga Chlamydomonas reinhardtii at different time points before the onset and during the course of ... More
RNA expression profiling at the single molecule level.
Authors:Hesse J, Jacak J, Kasper M, Regl G, Eichberger T, Winklmayr M, Aberger F, Sonnleitner M, Schlapak R, Howorka S, Muresan L, Frischauf AM, Schütz GJ,
Journal:Genome Res
PubMed ID:16809670
We developed a microarray platform for PCR amplification-independent expression profiling of minute samples. A novel scanning system combined with specialized biochips enables detection down to individual fluorescent oligonucleotide molecules specifically hybridized to their complementary sequence over the entire biochip surface of cm2 size. A detection limit of 1.3 fM target ... More
Transcriptomic signatures of alterations in a myoblast cell line infected with four distinct strains of Trypanosoma cruzi.
Authors:Adesse D, Iacobas DA, Iacobas S, Garzoni LR, Meirelles Mde N, Tanowitz HB, Spray DC,
Journal:Am J Trop Med Hyg
PubMed ID:20439965
We examined the extent to which different Trypanosoma cruzi strains induce transcriptomic changes in cultured L(6)E(9) myoblasts 72 hours after infection with Brazil (TC I), Y (TC II), CL (TC II), and Tulahuen (TC II) strains. Expression of 6,289 distinct, fully annotated unigenes was quantified with 27,000 rat oligonucleotide arrays ... More