Recombinant-Influenza-A-virus-
Matrix-protein-2MMatrix protein 2 Alternative name(s): Proton channel protein M2- ￥9576
- CUSABIO
- CN
- CSB-CF732264IEL
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
"-20°C/-80°C"
- 保质期：
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
- 英文名：
Customized Influenza A virus Matrix protein 2 (M) Protein (in vitro E.coli)
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 规格：
20ug
Alternative Name(s)
Matrix protein 2 Alternative name(s): Proton channel protein M2Editorial/Sponsord
EditorialUniprot ID
Q6DPU3Gene Names
Matrix protein 2 (M)Organism
Influenza A virusAASequence
ETPTRTGWECKCSDSSDPLVVAASIIGILHLILWILDRLFFKCIYRRLKYGLKRGPSTGG VPESMREEYRQEQQSAVDVDDGHFVNIELEExpression Region
1-90aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1368Purity
Greater than 85% as determined by SDS-PAGE.Storage Buffer
Tris/PBS-based buffer, 6% TrehaloseStorage
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.Endotoxin
Not Test. Endotoxin removal service is available for free upon you request.产品类型
Transmembrane-Protein备注
**产品信息可能有变动，请以官网信息为准
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文献和实验**产品信息可能有变动，请以官网信息为准
Alternative Bioreactor Strategy for Probing Infection and Production
Probing the baculovirus infection process is essential in optimizing the recombinant protein production. Typically, researchers monitor the infection process in the stirred tank reactor, which, however, contains a population of cells infected
Protein Production With Recombinant Baculoviruses in Lepidopteran Larvae
insect for recombinant protein production, and explore three different methods of virus administration to the larvae. The first method is labor-intensive, as extracellular virus is injected into each larva, whereas the second lends itself to infection
proteins.It is a convenient alternative to sonication for extracting recombinant proteins from the cytoplasm of Escherichia coli cells carrying expression vectors,especially when many proteins are to be processed in parallel. In this article I’ll summarize
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