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Merck

E0639

Sigma-Aldrich

内切糖苷酶F2 from Elizabethkingia miricola

recombinant, expressed in E. coli, 20 U/mg

别名:

内-β-N-乙酰氨基葡糖苷酶F2,Endo F2, 内切糖苷酶F2 来源于脑膜炎脓毒性黄杆菌, 内切糖苷酶F2 来源于脑膜脓毒性伊丽莎白菌, 内切糖苷酶F2 来源于脑膜脓毒性金黄杆菌, 米尔伊丽莎白菌

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0.2 UNIT
$684.00

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0.2 UNIT
$684.00

About This Item

CAS号:
MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.32

$684.00


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重组

expressed in E. coli

质量水平

偶联物

(N-linked)

表单

solution

比活

20 U/mg

分子量

32 kDa

运输

wet ice

储存温度

2-8°C

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相关类别

包装

提供 5× 反应缓冲液,250 mM 醋酸钠,pH 4.5

单位定义

一个单元将在37 °C、pH 4.5下每分钟从1 μmole变性猪纤维蛋白原释放N-连接寡糖。

外形

无菌灌装溶液,含10 mM乙酸钠、25 mM氯化钠,pH 4.5

储存分类代码

10 - Combustible liquids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Liv Anette Bøhle et al.
FEMS microbiology letters, 325(2), 123-129 (2011-11-19)
It has been demonstrated previously that Enterococcus faecalis produces secreted endoglycosidases that enable the bacteria to remove N-linked glycans from glycoproteins. One enzyme potentially responsible for this activity is EF0114, comprising a typical GH18 endoglycosidase domain and a GH20 domain.
Helena Ryšlavá et al.
The FEBS journal, 278(14), 2469-2484 (2011-05-14)
Fungal β-N-acetylhexosaminidases are inducible extracellular enzymes with many biotechnological applications. The enzyme from Penicillium oxalicum has unique enzymatic properties despite its close evolutionary relationship with other fungal hexosaminidases. It has high GalNAcase activity, tolerates substrates with the modified N-acyl group
Wei Zhang et al.
Talanta, 85(1), 499-505 (2011-06-08)
Endoglycosidase is a class of glycosidases that specifically cleaves the glycosidic bond between two proximal residues of GlcNAc in the pentasaccharide core of N-glycan, leaving the innermost GlcNAc still attached to its parent protein, which provides a different diagnostic maker
Valentina Botti et al.
PloS one, 6(8), e23838-e23838 (2011-08-23)
Hepatitis C Virus E1E2 heterodimers are components of the viral spike. Although there is a general agreement on the necessity of the co-expression of both E1 and E2 on a single coding unit for their productive folding and assembly, in
M V Padkina et al.
Prikladnaia biokhimiia i mikrobiologiia, 46(4), 448-455 (2010-09-29)
The HuIFNA16, HuIFNB, and BoIFNG genes encoding human [alpha]16, beta-interferons and bovine gamma-interferon were cloned under the control of the yeast Pichia pastoris AOX1 gene promoter. The yeast strains producing heterologous interferons intracellularly and extracellularly were constructed. There was no

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Explore strategies for releasing N-linked glycans with PNGase F, PNGase A & native & sequential deglycosylation with endoglycosidases & exoglycosidases.

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