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Merck

D9515

Sigma-Aldrich

Driselase崩溃酶 来源于担子菌

greener alternative

powder, Protein ≥10 % by biuret

别名:

cellulase, laminarinase, xylanase

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About This Item

CAS号:
EC號碼:
MDL號碼:
分類程式碼代碼:
12352204
NACRES:
NA.54

共軛

conjugate (Glucosaminoglycan)

品質等級

形狀

powder

成份

Protein, ≥10% biuret

環保替代產品特色

Waste Prevention
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

環保替代類別

運輸包裝

wet ice

儲存溫度

−20°C

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一般說明

我们致力于为您提供更环保的替代产品,以符合“绿色化学的12项原则”的一项或多项原则要求。当用于纤维素乙醇研究时,该产品经优化可提高能效和防止浪费。更多信息请参阅《Biofiles》《Enzymes for Alternative Energy Research》上的文章。

應用

Sigma的酶在检测对香豆素酯酶从完整的细胞壁释放对香豆素和阿魏罗伊尔基团的能力中被作为对照。它还被用于一项研究 炭疽菌 对玉米的致病性,并将其用于菌丝体原生质体的制备。
已有一项研究利用担子菌的崩溃酶,研究了具有不同阿魏酰化侧链的阿拉伯木聚糖被真菌糖酵素的消化特性。已有一项研究利用担子菌的崩溃酶,研究了汉诺半乳糖酸水解酶的纯化、表征和作用模式。

生化/生理作用

崩溃酶是由纤维素酶、半纤维素酶、果胶酶等组成的细胞壁降解酶。因此,它去除植物细胞壁来制造原生质体是非常有效的。

其他說明

粗体粉末中含有昆布多糖酶、木聚糖酶和纤维素酶。

法律資訊

Driselase is a trademark of ASKA Animal Health Co. Ltd.

象形圖

Health hazard

訊號詞

Danger

危險聲明

防範說明

危險分類

Resp. Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

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W S Borneman et al.
Applied and environmental microbiology, 57(8), 2337-2344 (1991-08-01)
An extracellular p-coumaroyl esterase produced by the anaerobic fungus Neocallimastix strain MC-2 released p-coumaroyl groups from 0-[5-0-((E)-p-coumaroyl)-alpha-L-arabinofuranosyl]-(1----3)-0-beta -D-xylopyranosyl-(1----4)-D-xylopyranose (PAXX). The esterase was purified 121-fold from culture medium in successive steps involving ultrafiltration column chromatography on S-sepharose and hydroxylapatite, isoelectric focusing
J S Scott-Craig et al.
The Plant cell, 2(12), 1191-1200 (1990-12-01)
A gene (PGN1) encoding extracellular endopolygalacturonase was isolated from the fungal maize pathogen Cochliobolus carbonum race 1. A probe was synthesized by polymerase chain reaction using oligonucleotides based on the endopolygalacturonase amino acid sequence. Genomic and cDNA copies of the
Taras Pasternak et al.
Plant methods, 11, 50-50 (2015-10-31)
Rapid advances in microscopy have boosted research on cell biology. However sample preparation enabling excellent reproducible tissue preservation and cell labeling for in depth microscopic analysis of inner cell layers, tissues and organs still represents a major challenge for immunolocalization
Q Chen et al.
Plant physiology, 94(4), 1820-1829 (1990-12-01)
Treating carrot (Daucus carota L.) suspension culture cells with a mixture of cell wall degrading enzymes, Driselase, resulted in an increase in the percentage of [(3)H]phosphatidylinositol bisphosphate. Analysis of the lipid kinase activities in the isolated plasma membranes after whole
G Wende et al.
Phytochemistry, 45(6), 1123-1129 (1997-07-01)
Alcohol-insoluble residues (AIRs) from Festuca and Zea cell cultures contained 7.4 and 35 nmol esterified ferulate mg-1, respectively. Driselase solubilised 79% of the feruloylated material from both AIRs. Of the feruloyl esters solubilised from Festuca and Zea AIRs, 72 and

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