219466
CELLULYSIN® Cellulase, Trichoderma viride
Sinónimos:
β-D-glucosidase, endo-β-1,4 glucanase, cellobiohydrolase
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About This Item
Número de CAS:
Número MDL:
Código UNSPSC:
12352202
NACRES:
NA.54
Productos recomendados
origen biológico
fungus (Trichoderma viride)
formulario
solid
actividad específica
≥10,000 units/g dry wt.
fabricante / nombre comercial
Calbiochem®
condiciones de almacenamiento
OK to freeze
técnicas
transformation: suitable
color
yellow-white
solubilidad
water: soluble
idoneidad
suitable for molecular biology
aplicaciones
food and beverages
pharmaceutical
Condiciones de envío
ambient
temp. de almacenamiento
2-8°C
Descripción general
Cellulase includes endo-β-1,4 glucanase, cellobiohydrolase, and β-D-glucosidase. It is commonly produced by bacteria and fungi.
Aplicación
CELLULYSIN® Cellulase, Trichoderma viride has been used:
- to digest transgenic BY-2 cells exposed to paraformaldehyde fixation
- in the enzyme mix used for in situ hybridization to plant chromosomes
- in the enzyme solution for the transformation of Phytophthora species
- to isolate intact cells and protoplasts from plant tissues
Acciones bioquímicas o fisiológicas
Cellulase is useful in food, feed, textile, leather, detergent, and paper industries. It is also applied in fiber modification, biomass fermentation, and pharmaceutical industries.
Advertencia
Toxicity: Harmful (C)
Definición de unidad
One unit is a measure of decomposing activity using a filter paper substrate at 40°C, pH 4.0.
Reconstitución
Following reconstitution, aliquot and freeze (-20°C) for long term storage or refrigerate (4°C) for short term storage. Stock solutions are stable for up to 3 days at 4°C or for up to 1 month at -20°C.
Otras notas
Takebe, I., et al. 1968. Plant Cell Physiol.9, 115.
Tomita, Y., et al. 1968. J. Ferment. Technol.46, 701.
Tomita, Y., et al. 1968. J. Ferment. Technol.46, 701.
Información legal
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
CELLULYSIN is a registered trademark of Merck KGaA, Darmstadt, Germany
Palabra de señalización
Danger
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Resp. Sens. 1
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 1
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Los clientes también vieron
Weizhen Wang et al.
Frontiers in microbiology, 10, 2402-2402 (2019-11-12)
Phytophthora, a genus of oomycetes, contains many devastating plant pathogens, which cause substantial economic losses worldwide. Recently, CRISPR/Cas9-based genome editing tool was introduced into Phytophthora to delineate the functionality of individual genes. The available selection markers for Phytophthora transformation, however
Farjana Islam et al.
BMC research notes, 11(1), 445-445 (2018-07-06)
This study was conducted to isolate, screening and purification of cellulase from bacteria present in sugar industry waste (molasses) and characterization by morphological and biochemical analysis. Based on experiments, three bacterial strains produced clear transparent zone into carboxymethyl cellulose (CMC)
In Situ Hybridization to Plant Chromosomes
Fluorescence In Situ Hybridization (FISH), 447-494 null
Man-Wah Li et al.
PloS one, 10(8), e0135033-e0135033 (2015-08-14)
Arabidopsis High Mobility Group Box (HMBG) proteins were previously found associated with the interphase chromatin but not the metaphase chromosome. However, these studies are usually based on immunolocalization analysis involving paraformaldehyde fixation. Paraformaldehyde fixation has been widely adapted to preserved
Rahman Ebrahimzadegan et al.
Scientific reports, 9(1), 19989-19989 (2019-12-29)
Here, we characterized the basic properties of repetitive sequences in essential A and supernumerary B chromosomes of Festuca pratensis Huds. This was performed by comparative analysis of low-pass Illumina sequence reads of B chromosome lacking (-B) and B chromosome containing
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