Team:Washington/Protocols

From 2013.igem.org

Cloning Protocols

• iGEM Vector Information
• General Cloning Strategy

Workflow:

• 1) Isolation of Plasmid DNA (miniprep)
• 2) General PCR Protocol (also see PCR GoTaq - product (30-200ng/ ul) Check on gel PCR Purification and/or Dpnl Digest
• 3) General Digestion Protocol Check on gel PCR Purification or Heat Inactivation (check enzyme temp and time, usually 80C for 20min)
• 4) Agarose Gel Electrophoresis
• 5) General Ligation Protocol (Don’t forget background control plates) Heat Inactivation (optional - up to 10 fold increase) - 65° for 10 minutes
• 6) Heat shock/chemical competent transformation
• 7) Colony PCR with Green taq Miniprep (stocks can be made from this culture - add 1ml extra)
• 9) Making Glycerol Frozen Stocks

Light Sensing Protocols

Light Sensing Media:

• 5X M9 Salts
• M9 Media + Casamino Acid Recipe
• M9 + Casamino Acid Plate

Light Testing:

• General Protocol
• 96-Well Plate Assay
• 60 mm Petri Dish Assay
• Fluorescent Analysis Protocol
• GFP Expression on Agar Plates
• Light Intensity Test
• Blinking Test

Setting Up The App:

• E.colight Setup

App Testing:

• Bleed-Through Test

Retrieved from "http://2013.igem.org/Team:Washington/Protocols"