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Merck

10113

Sigma-Aldrich

淀粉葡萄糖苷酶 来源于黑曲霉

greener alternative

powder, white, ~120 U/mg

别名:

1,4-α-D-葡聚糖葡萄糖水解酶, 糖化淀粉酶, 葡萄糖淀粉酶

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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

形狀

powder

比活性

~120 U/mg

分子量

Mr ~97000

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

顏色

white

異物活動

protease ≤0.1%

環保替代類別

儲存溫度

2-8°C

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相关类别

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。该产品针对淀粉水解研究进行了优化,可提高能效并防止浪费。有关详细信息,请参阅《Biofiles》的文章

單位定義

1 单位酶相当于在pH 值为 4.8、60℃条件下(淀粉,目录号85642,作为底物)每分钟释放1 μmol 葡萄糖的酶量。

其他說明

反式葡糖淀粉酶合成异寡糖

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)


分析证书(COA)

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R.A. Rastall et al.
Biotechnology Letters, 13, 501-501 (1991)
Yuping Chen et al.
Bio-protocol, 7(13), e2371-e2371 (2017-07-05)
Organisms store carbohydrates in several forms. In yeast, carbohydrates are stored in glycogen (a multi-branched polysaccharide) and in trehalose (a disaccharide). As in other organisms, the amount of stored carbohydrate varies dramatically with physiological state, and accordingly, an assay of
Tiziana Ventriglia et al.
Plant physiology, 148(1), 65-76 (2008-07-11)
ADP-glucose (Glc) pyrophosphorylase (ADP-Glc PPase) catalyzes the first committed step in starch biosynthesis. Higher plant ADP-Glc PPase is a heterotetramer (alpha(2)beta(2)) consisting of two small and two large subunits. There is increasing evidence that suggests that catalytic and regulatory properties
Lauren R Brewer et al.
Journal of agricultural and food chemistry, 60(17), 4379-4387 (2012-04-07)
To determine the rapidly digestible starch (RDS), slowly digestible starch (SDS), and resistant starch (RS) contents in a starch sample, the addition of amyloglucosidase is often used to convert hydrolyzates from α-amylase digestion to glucose. The objectives of this study
M I Nilsson et al.
Gene, 537(1), 41-45 (2014-01-05)
Pompe disease is a clinically and genetically heterogeneous autosomal recessive disorder caused by lysosomal acid α-glucosidase (GAA) deficiency. We report on two affected members of a non-consanguineous Caucasian family, including a classical infantile-onset patient with severe cardiomyopathy (IO) and his

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