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Merck
CN

N8271

α(2→3,6,8,9) 神经氨酸酶 来源于产脲节杆菌

recombinant, expressed in E. coli, buffered aqueous solution

别名:

神经氨酸酶 来源于产脲节杆菌, 唾液酸酶, 神经氨酸苷酶

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化学文摘社编号:
UNSPSC Code:
12352204
NACRES:
NA.32
MDL number:
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产品名称

α(2→3,6,8,9) 神经氨酸酶 来源于产脲节杆菌, recombinant, expressed in E. coli, buffered aqueous solution

recombinant

expressed in E. coli

form

buffered aqueous solution

specific activity

≥135 units/mg protein

mol wt

88 kDa
95 kDa

foreign activity

β-Galactosidase, α-mannosidase, β-hexosaminidase, α-fucosidase, and proteases, none detected

shipped in

wet ice

storage temp.

2-8°C

Quality Level

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Packaging

本品为5倍浓缩的反应缓冲液(250 mM磷酸钠,pH 6.0)。

Physical form

溶于20mM Tris-HCl (pH 7.5)和20 mM NaCl的溶液中。

Preparation Note

表达于无糖苷酶的宿主中。

Biochem/physiol Actions

从复合寡糖中释放α(2→3)、α(2→6)、α(2→8)和 α(2→9)-连接的N-乙酰神经氨酸。

Other Notes

一个酶活性单位是指在pH 5.0、37℃下,每分钟水解1 μmole的4-甲基伞形酮α-D-N-乙酰神经氨酸苷所需的酶量。

存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Interactions that facilitate transmembrane domain (TMD) dimerization have been identified mainly using synthetic TMDs. Here, we investigated how inherent properties within natural TMDs modulate their interaction strength by exploiting the sequence variation in the nine neuraminidase subtypes (N1-N9) and the
Audu J Natala et al.
Journal of medical entomology, 50(1), 85-93 (2013-02-23)
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Nature, 508(7495), 254-257 (2014-02-18)
Zoonotic infectious diseases such as influenza continue to pose a grave threat to human health. However, the factors that mediate the emergence of RNA viruses such as influenza A virus (IAV) are still incompletely understood. Phylogenetic inference is crucial to reconstructing
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The Medical journal of Australia, 198(7), 370-372 (2013-04-16)
To review cases of nosocomial influenza and compare the epidemiology, clinical characteristics and outcomes with community-acquired cases. Prospective case series of adults hospitalised with influenza during April - November of 2010 and 2011 using a hospital-based sentinel surveillance system. A

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