Sample is bacterial cells from agar plate colony, liquid media culture, or glycerol stock. This protocol is designed for mid- to high-copy number plasmids (> 10 copies per cell). You must also supply sequencing primer(s) or select some of our universal primers.
Primer requirements:
Sample requirements:
Template |
Preparation |
Plasticware |
Bacterial colony |
Using a pipette tip, pick a bacterial colony from an agar plate. Resuspend it in 10 µl low TE buffer or nuclease-free water. |
Please use 96-well plates or 8-tube strips. Secure plates preferably with lids, avoid adhesive foil which may not be safe enough to prevent spillage. We recommend 8-tube strips with individual caps (eg Eppendorf 0030124359). Do not use parafilm. Please mark the tubes preferably with a number indicating their order in the order form. |
Liquid culture or glycerol stock |
Transfer 1 µl of bacterial culture or glycerol stock to 9 µl low TE buffer or nuclease-free water. |