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Citas y referencias (5)
Invitrogen™
EnzChek™ Cellulase Substrate, blue fluorescent, 339/452
El sustrato de celulasa EnzChek™ se desarrolló para la cuantificación simple y rápida de celulasa. El ensayo se puede completarMás información
| Número de catálogo | Cantidad |
|---|---|
| E33953 | 1 mg |
Número de catálogo E33953
Precio (USD)
-
Cantidad:
1 mg
El sustrato de celulasa EnzChek™ se desarrolló para la cuantificación simple y rápida de celulasa. El ensayo se puede completar en 30 minutos o menos. Simplemente mezcle la enzima con la solución de trabajo de sustrato de celulasa EnxChek™, incube y lea los resultados usando la excitación/emisión máxima de ∼ 339/452 nm. A diferencia de otros ensayos de varios pasos más complejos, el sustrato de celulasa EnzChek™ es perfecto para su uso en un entorno de alto rendimiento. Este sustrato de fluorescencia es muy sensible, con un límite de detección de tan solo 40 μU/ml de celulasa. También es posible utilizar este sustrato en un ensayo colorimétrico, aunque con sensibilidad reducida.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Para utilizar con (equipo)Fluorímetro, lector de microplacas
Línea de productosEnzChek
Cantidad1 mg
Condiciones de envíoTemperatura ambiente
SustratoSustrato de celulasa
Método de detecciónColorimétrico, fluorescente
FormularioSólido
Substrate PropertiesSustrato químico
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
A novel system for trigger-controlled drug release from polymer capsules.
Journal:J Control Release
PubMed ID:18755229
'Technologies currently available for the controlled release of protein therapeutics involve either continuous or tissue-specific discharge from implants or engineered extracellular matrix mimetics. For some therapeutic applications the trigger-controlled release of protein cargo from a synthetic implant could be highly desirable. We have designed the CellEase technology, a two-component system
Identification of a Novel Garlic Cellulase Gene.
Journal:
PubMed ID:24415833
Genes encoding cellulase enzymes have been investigated in various plants due to the importance of cellulase enzymes in industrial applications, especially in the conversion of biomass into biofuels. Although several cellulase genes have been cloned and characterized, little is known about cellulase genes from garlic or enzyme activities of their
Deletion of creB in Aspergillus oryzae Increases Secreted Hydrolytic Enzyme Activity.
Journal:
PubMed ID:23835170
Aspergillus oryzae has been used in the food and beverage industry for centuries, and industrial strains have been produced by multiple rounds of selection. Targeted gene deletion technology is particularly useful for strain improvement in such strains, particularly when they do not have a well-characterized meiotic cycle. Phenotypes of an
Disruption of Trichoderma reesei cre2, encoding an ubiquitin C-terminal hydrolase, results in increased cellulase activity.
Journal:BMC Biotechnol
PubMed ID:22070776
The filamentous fungus Trichoderma reesei (Hypocrea jecorina) is an important source of cellulases for use in the textile and alternative fuel industries. To fully understand the regulation of cellulase production in T. reesei, the role of a gene known to be involved in carbon regulation in Aspergillus nidulans, but unstudied
Lipid-modifying enzymes in human tear fluid and corneal epithelial stress response.
Journal:
PubMed ID:24302584
Since homeostasis at the ocular surface requires a delicate balance between numerous factors, and the external environment contributes as an unpredictable component, we aimed to understand the role that various lipids and their regulators have in the complex process that maintains a healthy corneal surface. Through basic proteomics, we tested