915
edits
Changes
filled in protocol from http://www.oligoengine.com/products/psuper/documentation/protocols/pSUPER_protocol.pdf
Where:
*<span style="color: #FF0000">XbaI BglII compatible overhang</span>
*<span style="color: #00FFFF">Spacer</span>
*<span style="color:#FFD700">Loop</span>
For the reverse primer choose the reverse complement, remove the XbaI overhang from the 3' end (the last GATC sequence) and add an AGTC sequence to the 5' end (for HindIII).
Order primers through IDT-DNA
==Cloning Targetting Construct==
*see http://www.oligoengine.com/products/psuper/documentation/protocols/pSUPER_protocol.pdf
===Digestion of pAdtrack-H1 Promoter (or pSuper)===
#If using a BglII/HindII do a sequential digestion
#Combine 1ug plasmid , 1uL HindIII and water/buffer to 50 uL (use NEB buffer 2)
#Incubate 1h at 37C
#Add 1uL BglII
#Incubate 2h at 37C
#There is no need to CIP treat, but this can be done if too many false positives are found.
#Gel purify the digested fragment and adjust to 0.2-0.5 mg/mL.
===Annealing Primers===
#Dissolve oligos to 3 mg/mL
#Combine 1 uL of each oligo + 48 uL annealing buffer (100 mM NaCl and 50 mM HEPES pH 7.4.) into a PCR tube.
#Run program '''annealing'''
##90C for 4min
##70C for 10min
##Gradient to 37C for 20 min
##4C for storage
#Store at -20 or 4C
===Ligation===
#Combine 2uL annealed oligos with 1uL vector, 2.5uL 4X ligase buffer 4.5 uL water and 1 uL T4 Ligase
#Incubate overnight at room temperature
#Perform negative selection by adding 1 uL BglII and incubating at 37C for 30min (this removes single cut or uncut vector).
#Transform into subcloning efficiency DH5a cells
===Checking for Positive Clones===
#Miniprep clones
#Digest with EcoRI/HindIII for 1h
#Run on a gel. Positive clones are 281bp, negative clones are 227bp
#Sequence positive clones with pAdtrack sequencing primer.
