无菌性
aseptically filled
表单
lyophilized powder
比活
≥2 units/mg solid
储存温度
2-8°C
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应用
可用于植物原生质体的制备,以在细胞器分离之前消化细胞壁。
其他说明
据报道,其含有两种类型的果胶酶、内切多聚半乳糖醛酸酶(EC3.2.1.15)、内切蛋白裂解酶(EC4.2.2.10)以及浸渍刺激因子。
View more information on enzymes for complex carbohydrate analysis at www.sigma-aldrich.com/enzymeexplorer
单位定义
One unit will liberate 1.0 μmole of galacturonic acid from polygalacturonic acid per min at pH 5.5 at 25 °C.
外形
Lyophilized powder containing lactose
制备说明
Prepared from P 3026
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
BMC evolutionary biology, 12, 195-195 (2012-10-03)
Gene duplications are a molecular mechanism potentially mediating generation of functional novelty. However, the probabilities of maintenance and functional divergence of duplicated genes are shaped by selective pressures acting on gene copies immediately after the duplication event. The ratio of
BMC genomics, 13, 321-321 (2012-07-21)
Pectins are diverse and very complex biomolecules and their structure depends on the plant species and tissue. It was previously shown that derivatives of pectic polymers and oligosaccharides from pectins have positive effects on human health. To obtain specific pectic
BMC plant biology, 12, 150-150 (2012-08-28)
Cell separation that occurs during fleshy fruit abscission and dry fruit dehiscence facilitates seed dispersal, the final stage of plant reproductive development. While our understanding of the evolutionary context of cell separation is limited mainly to the eudicot model systems
Genetics and molecular research : GMR, 11(3), 3091-3104 (2012-09-26)
Molecular chaperones of plasmid pBI121 carrying CaMV35S promoter and a nucleotide sequence of plasmid pBI221 were inserted into plasmid pCAMBIA2300 to construct an intermediate vector: pVBG2307. This novel vector pVBG2307 contains a greatly expanded multiple cloning site with an adjacent
Applied biochemistry and biotechnology, 169(1), 215-227 (2012-11-28)
The aim of the present study was to investigate pectinases production by CT1 mutant of Penicillium occitanis on glucose based media. Two main groups of pectinases were followed: lyases (pectin and pectate lyases) and hydrolases (polygalacturonases and polymethylgalacturonases). When cultivated
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