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Functional Reconstitution of Intracellular Vesicle Fusion Using Purified SNAREs and Sec1/Munc18 (SM) Proteins.

Yu H, Crisman L, Stowell MHB, Shen J
Methods Mol Biol. 2019;1860:237-249. doi: 10.1007/978-1-4939-8760-3_15. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
135550pET-28a-His6-SUMO-Munc18-1wtExpress rat Munc18-1 in E. coli BL21, purified via HisPur Ni-NTA Resin
135551pET-28a-His6-SUMO-VAMP2Express mouse VAMP2 in E. coli BL21, purified via HisPur Ni-NTA Resin
135552pET-28a-His6-SUMO-VAMP3Express rat VAMP3 in E. coli BL21, purified via HisPur Ni-NTA Resin
135553pET-28a-His6-SUMO-VAMP8Express mouse VAMP8 in E. coli BL21, purified via HisPur Ni-NTA Resin
135554pFastBac HT JS-Munc18bExpress rat Munc18b in Sf9 cells, the resulted plasmid encodes an N-terminally His6-tagged Munc18c protein with a tobacco etch virus (TEV) cleavage site between the His6 tag and Munc18b.
135555pFastBac HT JS-Munc18cExpress mouse Munc18c in Sf9 cells, the resulted plasmid encodes an N-terminally His6-tagged Munc18c protein with a tobacco etch virus (TEV) cleavage site between the His6 tag and Munc18c.

Antibodies from Article