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Comment: Task marked complete

ToDoTo Do:

Friday:

  •  Nanodrop pENTR (was not useful)
  •  Transform pENTR into bacteria
  •  Incubate over night
  •  (5pm) Add Kan, incubate GGDonr liq culture (16hrs)

Saturday:

  •  Remove GGDonr liq culture from incubator (9am)
  •  Make cell stock, store at -80 degrees
  •  Put rest of cell culture in 4 degrees
  •  Remove pENTR cultures from incubator (10:30am, Shinjini)
  •  Pick cells from pENTR colonies, put in liquid culture, put in incubator at 12pm
  •  Pick cells from pENTR colonies (when?) , put in liquid culture, put in incubator at 5:30pm (16 hours)

...

Sunday:

  •  Take pENTR colonies from incubator. Make cell stock. Put in fridge and freezer respectively. (10 am). Did not work.

Monday:

  •  Make empty liquid cell culture to transform DNA into (~16hours) Make 5 femptomolal Miniprep GGDonr (is that a good idea?)
  •  Pick Cells again and incubate (at 6pm)

...

Tuesday:

  •  Miniprep pENTRs
  •  Make 5 femptomolar working solution
  •  LR (~ 16 hours min, 24 max) Monday
  •  Miniprep GGDonr PCR (possibly)



June 9

Plan of Action

...

 
Making LilrB2/PirB expression vectorsStart DateProgress/condition/next stepsCompleted? (Date)ResultLocation of part (if needed, I don't know)

Making pENTR from gBlocks:

We have:
Q1_LilrB2_Qx
Q1_PirB-N_Q2, Q2_PirB-C_Qx

We need:
pGGDONR : has Q1 and Qx sites, L1 and L2 sites

Golden-gating will result in:
pENTR_L1_LilrB2_L2 (order of L's correct, I checked!)
pENTR_L1_PirB2_L2

6/12  GG mixtures in thermocycler

GGDonr cell (culture?) in incubator

Will make GGDonr bacterial stock today (6/13)

   fridge (in case transformations did not work)

After that, Gateway (LR):
pENTR_L1_LilrB2_L2
pENTR_L4_Hef1a_R1 (not sure if this is the one we want)
pZDonor 1-GTW-2 (this is the DEST Shinjini used in her Geneious)

Same for PirB
pENTR_L1_PirB_L2
pENTR_L4_Hef1a_R1
pZDonor 1-GTW-2

We will get:

12_Hef1a_LilrB2
12_Hef1a_PirB

    


6/12/14

GoldenGate table:

...