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- 库存：
100
- 供应商：
无锡莱弗思生物实验器材有限公司
- 规格：
5 mg
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文献和实验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
. Kalmar, B., Novoselov, S., Gray, A., Cheetham, M.E., Margulis, B., and Greensmith, L. 2008. Late stage treatment with arimoclomol delays disease progression and prevents protein aggregation in the SOD1 mouse
Strategies to Optimize Protein Expression in E. coli
. 2007. Purification and initiation of structural characterization of human peripheral myelin protein 22, an integral membrane protein linked to peripheral neuropathies. Biochemistry 46:11185‐11195.
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