- ￥1080 - 25000
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- pro-466
- 2026年01月17日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
for future use below -18°C
- 保质期：
See instructions
- 英文名：
MOG
- 库存：
常规产品有备货
- 供应商：
上海经科化学科技有限公司
- CAS号：
无
- 规格：
10ug/50ug/1mg
| 规格： | 10ug | 产品价格： | ￥1080.0 |
|---|---|---|---|
| 规格： | 50ug | 产品价格： | ￥2415.0 |
| 规格： | 1mg | 产品价格： | ￥25000.0 |
CATALOGUE NUMBER
PRO-466
SYNONYMS
INTRODUCTION
DESCRIPTION
SOURCE
PHYSICAL APPEARANCE
FORMULATION
The Myelin Oligodendrocyte Glycoprotein was lyophilized from a 0.2µm filtered solution in 20mM HAc-NaAc and 150mM NaCl pH-4.5
SOLUBILITY
|
It is recommended to reconstitute the lyophilized MOG in sterile 50mM Acetic acid not less than 100µg/ml, which can then be further diluted to other aqueous solutions. |
STABILITY
For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).
Please prevent freeze-thaw cycles.
PURITY
|
Greater than 95.0% as determined by SDS-PAGE. |
AMINO ACID SEQUENCE
GKDQDGDQAPEYRGRTELLKDAIGEGKVTLRIRNVRFSDEGGFTCFFRDHSYQE
EAAMELKVEDPFYWVSPGHHHHHH.
SAFETY DATA SHEET
SDS
USAGE
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文献和实验Myelin Oligodendrocyte Glycoprotein produced in E.Coli is a single, non-glycosylated polypeptide chain containing a total of 132 amino acids (Met + 30-154 a.a. + 6x His tag at C-terminus) and having a total molecular mass of 15.2 kDa.
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
Investigation of Astrocyte Oligodendrocyte Interactions in Human Cultures
Multiple sclerosis (MS) is characterized by CNS demyelination and oligodendrocyte depletion, axonal loss, and reactive astrogliosis. Myelin loss causes conduction block, while remyelination is associated with recovery
Transplantation of Oligodendrocyte Progenitor Cells in Animal Models of Leukodystrophies
as a curative therapy. Animal models of leukodystrophies have been valuable in developing effective strategies of myelin repair in human diseases. This chapter discusses the animal models of leukodystrophies and describes methods for (a) derivation of mouse
技术资料
