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Citas y referencias (5)
Invitrogen™
Alexa Fluor™ 647 Decapack Set
El Decapack de tinte reactivo Alexa Fluor® 647 está optimizado para su uso con técnicas de etiquetado de aminoalilo. ElMás información
| Número de catálogo | Cantidad |
|---|---|
| A32757 | 1 juego |
Número de catálogo A32757
Precio (MXN)
-
Cantidad:
1 juego
El Decapack de tinte reactivo Alexa Fluor® 647 está optimizado para su uso con técnicas de etiquetado de aminoalilo. El embalaje de un solo uso del colorante reactivo elimina la necesidad de alícuotas a granel, proporcionando comodidad y asegurando la máxima actividad de los colorantes. El colorante Alexa Fluor® 647 especialmente empaquetado es compatibles con nucleótidos modificados con aminoalilo dUTP y aminoalilo UTP, así como con la mayoría de los kits de etiquetado disponibles comercialmente a base de aminoalilo.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Método de etiquetadoEtiquetado indirecto
Etiqueta o tinteColorante Alexa Fluor
Línea de productosAlexa Fluor
Tipo de productoColorante reactivo
Cantidad1 juego
Condiciones de envíoTemperatura ambiente
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de -5 a -30 °C) y proteger de la luz.
Citations & References (5)
Citations & References
Abstract
Possible sources of dye-related signal correlation bias in two-color DNA microarray assays.
Journal:Anal Biochem
PubMed ID:15265729
'DNA microarray analyses commonly use two spectrally distinct fluorescent labels to simultaneously compare different mRNA pools. Signal correlation bias currently limits accepted resolution to twofold changes in gene expression. This bias was investigated by (i) examining fluorescence and absorption spectra and changes in relative fluorescence of DNAs labeled with the
Design of recombinant antibody microarrays for complex proteome analysis: choice of sample labeling-tag and solid support.
Journal:Proteomics
PubMed ID:17787036
Antibody-based microarray is a novel technology with great potential within high-throughput proteomics. The process of designing high-performing antibody (protein) microarrays has, however, turned out to be a challenging process. In this study, we have developed further our human recombinant single-chain variable-fragment (scFv) antibody microarray methodology by addressing two crucial technological
Effects of atmospheric ozone on microarray data quality.
Journal:Anal Chem
PubMed ID:14632079
A data anomaly was observed that affected the uniformity and reproducibility of fluorescent signal across DNA microarrays. Results from experimental sets designed to identify potential causes (from microarray production to array scanning) indicated that the anomaly was linked to a batch process; further work allowed us to localize the effect
CpG Island microarray probe sequences derived from a physical library are representative of CpG Islands annotated on the human genome.
Journal:Nucleic Acids Res
PubMed ID:15911630
An effective tool for the global analysis of both DNA methylation status and protein-chromatin interactions is a microarray constructed with sequences containing regulatory elements. One type of array suited for this purpose takes advantage of the strong association between CpG Islands (CGIs) and gene regulatory regions. We have obtained 20,736
Whole-genome DNA microarray analysis of a hyperthermophile and an archaeon: Pyrococcus furiosus grown on carbohydrates or peptides.
Journal:J Bacteriol
PubMed ID:12813088
The first complete-genome DNA microarray was constructed for a hyperthermophile or a nonhalophilic archaeon by using the 2,065 open reading frames (ORFs) that have been annotated in the genome of Pyrococcus furiosus (optimal growth temperature, 100 degrees C). This was used to determine relative transcript levels in cells grown at