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Wholemount ImmunoflurescentWholemount Immunoflurescent
Use4mlpolycarbonatesnap-captubesforallsteps.Rockingoftubesshouldbeperformedatalltimes.Allstepsarecarriedoutatroomtemperatureunlessotherwisestated.
Day0
1.Dissectembryosinice-coldPBS.RemoveasmuchextraembryonicmembranesaspossIBLe.Puncturetheamnionandinolderembryos(>E10)puncturetheheadwithasyringeortungstenneedle.
2.Fixin4%paraformaldehyde(PFA)inPBSat4oCovernight.
3.Washtwicefor5-10minutesinPBS.
4.Washwith50%MeOH/PBS,thentwicein100%MeOHfor5-15mineach.
Embryoscanbestoredat—20oCatthispoint,foruptoafewmonths.
Day1
5.IncubateembryosinfreshlypreparedMeOH:DMSO:H2O2(4:1:1)atroomtemperaturefor5-10hours.
Atthispointembryoscanbetakeninto100%MeOHandstoredat—20Catthispoint.
6.Rehydratetheembryosinaseriesof50%MeOH(20min)->PBS(2x15min)->freshlypreparedice-coldPBSMT(2x15min,1x1-2hour).
7.IncubatewithprimaryantibodyinPBMSTat4oCovernight.
Theantibodyincubationcanbeextendedforseveralovernightswithoutcompromisingtheexperiment.
Day2
8.Washwithfreshlypreparedice-coldPBMST(2x15min,5x1hour).
KeepPBMSTonice,orinfridge,butperformthewashesatroomtemperature.
9.Incubatewithsecondaryantibody(FITCcoupledforgreen,orCy5,Cy3coupledforred)inPBSMTat4oCovernight.
Theantibodyincubationcanbeextendedforseveralovernightswithoutcompromisingtheexperiment.
Day3
10.Washasinstep8.
11.RinseinPBT(2x10min).
12.Viewandphotographunderepifluorescenceoptics,forexamplefromBLS,Leica,orZeiss.
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