SMD1168H strain毕赤酵母菌株表达宿主菌 BioVector NTCC质粒载体菌种细胞基因保藏中心
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SMD1168H strain毕赤酵母菌株表达宿主菌 BioVector NTCC质粒载体菌种细胞基因保藏中心 SMD1168H strain
Description
Several Pichia pastoris strains are available to allow you to optimize expression and recovery of your protein of interest.
Table 2 provides information to help you choose the appropriate strain
SMD1168H (pep4)
Application
Selection of Zeocin resistant expression vectors to generate strains without protease A activity.
Recovery
1. Obtain an YPD agar plate.
2. Using a sterile pipette tip, touch the bacteria growing within the punctured area of the stab culture. (A sterilized wire loop or sterile toothpick can be used in place of a sterile pipette tip.)
3. Run this tip lightly over a section of the plate, as shown in the figure, to create streak #1.
4. Using another sterile pipette tip, pass through streak #1 and spread the bacteria over a second section of the plate, to create streak #2.
5. Using a third sterile pipette tip, pass through streak #2 and spread the bacteria over the last section of the plate, to create streak #3.
6. Grow overnight in a 30 o C incubator (unless a different growth temperature is indicated on the plasmid datasheet).
7. In the morning, single colonies should be visible. If the bacterial growth is too dense, re-streak onto a new agar plate to obtain single colonies.
BioVector NTCC质粒载体菌种细胞蛋白抗体基因保藏中心
电话:+86-010-53513060
网址:www.biovector.net [Supplier来源] http://www.biovector.net
Description
Several Pichia pastoris strains are available to allow you to optimize expression and recovery of your protein of interest.
Table 2 provides information to help you choose the appropriate strain
SMD1168H (pep4)
Application
Selection of Zeocin resistant expression vectors to generate strains without protease A activity.
Recovery
1. Obtain an YPD agar plate.
2. Using a sterile pipette tip, touch the bacteria growing within the punctured area of the stab culture. (A sterilized wire loop or sterile toothpick can be used in place of a sterile pipette tip.)
3. Run this tip lightly over a section of the plate, as shown in the figure, to create streak #1.
4. Using another sterile pipette tip, pass through streak #1 and spread the bacteria over a second section of the plate, to create streak #2.
5. Using a third sterile pipette tip, pass through streak #2 and spread the bacteria over the last section of the plate, to create streak #3.
6. Grow overnight in a 30 o C incubator (unless a different growth temperature is indicated on the plasmid datasheet).
7. In the morning, single colonies should be visible. If the bacterial growth is too dense, re-streak onto a new agar plate to obtain single colonies.
BioVector NTCC质粒载体菌种细胞蛋白抗体基因保藏中心
电话:+86-010-53513060
网址:www.biovector.net [Supplier来源] http://www.biovector.net
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