Recombinant-Bovine-Peripheral-
myelin-protein-22PMP22Peripheral myelin protein 22; PMP-22 Alternative name(s): PAS positive glycoprotein; PASII- ￥10206
- CUSABIO
- CN
- CSB-CF018241BO
- 2025年07月12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 Bovine PMP22 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)
Peripheral myelin protein 22; PMP-22 Alternative name(s): PAS positive glycoprotein; PASIIEditorial/Sponsord
EditorialUniprot ID
Q9TQZ3Gene Names
PMP22Organism
BovineAASequence
MLLLLLGIIVLHVAVLVLLFVSTIVSQWMVGNGHATDLWQNCSTSLMGSVQHCFSSSANE WLQSVQATMILSIIFSVLSLFLFFCQLFTLTKGGRFYITGVFQILAGLCVMSAASIYTVR HPEWHFNSDGSYGFAYILAWVAFPLALLSGVIYVILRKREExpression Region
1-160aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1458Purity
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
Expression and Secretion of a Soluble Form of Myelin-Associated Glycoprotein (MAG)
Myelin-associated glycoprotein (MAG) was first identified as the major glycoprotein in the central nervous system (CNS) through 3 Hfucose-labeling experiments (1 ). It is expressed on the surface of glial cells of both the CNS and peripheral
The COS-7 Cell In Vitro Paradigm to Study Myelin Proteolipid Protein 1 Gene Mutations
of proteolipid protein 1 (PLP1) in transiently transfected COS-7 cells. In humans, the PLP1 gene is located on the long arm of the X-chromosome and deletion, duplication, or coding region mutations in this gene cause the leukodystrophy, Pelizaeus-Merzbacher
to further separate and visualize the protein pattern of the peroxisomal subfractions of matrix, peripheral and integral membrane proteins. The identification of the known peroxisomal membrane proteins PMP22, PMP70 as well as mGST in the subsequent matrix-assisted
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