D8037
Driselase™ Basidiomycetes sp.
suitable for plant cell culture, BioReagent
Synonyme(s) :
Driselase™ from Basidiomycetes sp.
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About This Item
Numéro CAS:
Numéro CE :
Numéro MDL:
Code UNSPSC :
10171502
Nomenclature NACRES :
NA.72
Produits recommandés
Gamme de produits
BioReagent
Niveau de qualité
Forme
powder
Composition
Protein, ≥10% biuret
Technique(s)
cell culture | plant: suitable
Application(s)
agriculture
Température de stockage
−20°C
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Application
Driselase™ Basidiomycetes sp. has been used:
- in spheroplast preparation from Coccomyxa cells
- in a CRISPR/Cas9-based mutagenesis protocol for Brachypodium distachyon and its allopolyploid relative, Brachypodium hybridum
- for cell wall digestion to perform whole-mount immunolocalization of Lotus japonicus root tissue
Actions biochimiques/physiologiques
Driselase™ is a natural mixture of enzyme activities (fungal carbohydrates) used to digest plant cell walls to facilitate the maceration of plant materials, protoplast formation, and extraction processes. Driselase releases cell wall carbohydrates. This formulation contains enzyme activities of cellulose, endo-1,3-β-glucanase, and xylanase.
Autres remarques
Crude powder containing laminarinase, xylanase and cellulase.
Informations légales
Driselase is a trademark of ASKA Animal Health Co. Ltd.
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Resp. Sens. 1
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Les clients ont également consulté
Laura A Moody et al.
The New phytologist, 218(3), 1270-1277 (2018-03-03)
Forward genetics is now straightforward in the moss Physcomitrella patens, and large mutant populations can be screened relatively easily. However, perturbation of development before the formation of gametes currently leaves no route to gene discovery. Somatic hybridization has previously been
D T Kaplan et al.
Journal of nematology, 22(3), 399-406 (1990-07-01)
Radopholus spp. were reared in carrot tissue culture via established procedures, with slight modification. Several plant tissue maceration enzymes and flotation media (salts and sucrose) were evaluated with regard to nematode toxicity and extraction efficiency. Best extraction of viable nematodes
D P Blowers et al.
Plant physiology, 86(2), 505-509 (1988-02-01)
Plasma membrane vesicles from wild carrot cells grown in suspension culture were isolated by aqueous two-phase partitioning, and ATP-dependent phosphorylation was measured with [gamma-(32)P]ATP in the presence and absence of calcium. Treatment of the carrot cells with the cell wall
T Ishii et al.
Carbohydrate research, 248, 179-190 (1993-10-04)
Hydrolysis of spinach-leaf cell walls with Driselase (a fungal enzyme preparation) released two arabino-oligosaccharides and one galactobiose, each carrying a ferulic acid moiety. The oligosaccharides were characterized by NMR spectroscopy, methylation analysis, and FABMS. They were O-(2-O-trans-feruloyl-alpha-L-arabinofuranosyl)-(1-->5)-L-arabinof uranose, O-(6-O-trans-feruloyl-beta-D-galactopyranosyl)-(1-->4)-D-galactopy ranose
Ricardo Enrique Grados-Torrez et al.
International journal of molecular sciences, 22(17) (2021-09-11)
The membrane domain of eukaryotic HMG-CoA reductase (HMGR) has the conserved capacity to induce endoplasmic reticulum (ER) proliferation and membrane association into Organized Smooth Endoplasmic Reticulum (OSER) structures. These formations develop in response to overexpression of particular proteins, but also
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