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Citations & References (5)
Invitrogen™
EnzChek™ Cellulase Substrate, blue fluorescent, 339/452
The EnzChek™ cellulase substrate was developed for simple and rapid quantitation of cellulase. The assay can be completed in 30Read more
| Catalog Number | Quantity |
|---|---|
| E33953 | 1 mg |
Catalog number E33953
Price (BRL)
2.528,06
Each
Quantity:
1 mg
Price (BRL)
2.528,06
Each
The EnzChek™ cellulase substrate was developed for simple and rapid quantitation of cellulase. The assay can be completed in 30 minutes or less. Simply mix the enzyme with the EnxChek™ cellulase substrate working solution, incubate, and read the results using excitation/emission maxima ∼339/452 nm. In contrast to other more complex, multistep assays, the EnzChek™ cellulase substrate is perfect for use in a high-throughput environment. This fluorescence substrate is highly sensitive, with a detection limit as low as 40 μU/mL cellulase. It is also possible to use this substrate in a colorimetric assay, albeit with reduced sensitivity.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
For Use With (Equipment)Fluorometer, Microplate Reader
Product LineEnzChek
Quantity1 mg
Shipping ConditionRoom Temperature
SubstrateCellulase substrate
Detection MethodColorimetric, Fluorescence
FormSolid
Substrate PropertiesChemical Substrate
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
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