Product Data Sheet

Standard heat-shock transformation of chemically competent bacteria

1. Take competent cells out of -80°C and thaw on ice.
2. Take agar plates (containing the appropriate antibiotic) out of 4°C to warm up to room temperature or place in 37°C incubator.
3. Mix 5μl of DNA into 100μL competent cells in a microcentrifuge or falcon tube. GENTLY mix by flicking the bottom of the tube with your finger a few times.
4. Place the competent cell/DNA mixture on ice for 20-30min.
5. Heat shock each transformation tube by placing the bottom 2/3 of the tube into a 42°C water bath for 42 seconds. Put the tubes back on ice for 2 min.
6. Add 250-500μl SOC media (without antibiotic) and grow in 37°C shaking incubator for 45min.
7. Plate all of the transformation onto a 10cm LB agar plate containing the appropriate antibiotic.
8. Incubate plates at 37°C overnight.

Backbone

Vector backbone  pComb3X

Backbone size w/o insert (bp) 3300

Vector type  Bacterial Expression ; phage display

Growth in Bacteria

Bacterial Resistance(s)  Ampicillin

Growth Temperature  37°C

Growth Strain(s)  XL1 Blue

Copy number  High Copy

Gene/Insert

Gene/Insert name  TT Fab

Alt name&