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先全基因敲除再条件性基因敲除
Youwillneedthefollowingsolutions: PBS(Phosphate-BufferedSaline,Ca/Mgfree):- N.B.:Na2HPO4.2H2Ocanalsobeused->add1.42gfor1xand14.2gfor10xPBS.Makeupto1litrewithddH2O. PBSwash:- 100ml1xPBS10ulTween(0.01%,finalconcentration) Citrate/AcetateBufferpH6.0:- Sodiumacetate-4.1g.ddH2O-500ml. 2.100ml0.1MCitricacid Citricacid-2.1g.ddH2O-100ml. Titrate1with2toafinalpHof6.0.Citrate/AcetateBuffer,pH6canbestoredfrozenat-20°C. TMBSolution-10mg/mlinDMSO(storeat4°C). ThefollowingdetailsthemethodforusewithTMBasthesubstrate(coverwellswithclingfilmduringincubationstopreventevaporation). 1)Add3ulH2O2to20mlofCitrate/Acetatebuffer.Toevery5mlofbufferadd50ulTMBsolution.N.B.:Colourchangeisfromcolourlesstoblue(yellowwhenacidisadded). 2)Coatplatewithantigenstocksolution(1ug/mlinPBS,50ul/well)foratleast24hrsorovertheweekendat4°CorO/Nat37°C. 3)Removeantigenandwash3xwith1xPBS. 4)Blockwith1%BSA(100ul/well)in1xPBSforatleast1hrat37°C. 5)RemoveBSAbyflickingplate. 6)Wash3xwith1xPBScontaining0.01%tween 7)Addanti-serum(dilutedasappropiate,1/100etc.with1xPBS)andincubatefor2hrs@37°C.N.B.:Usepositiveandnegativecontrols. 8)Wash4xwith1xPBScontaining0.01%tween. 9)Addperoxidaseconjugate(50ul/well)diluted1:1000with1%BSA(dilutedinwashingsolutionasin8))andincubatefor1hr@37°C.N.B.:UsePRAM(Peroxidase-conjugatedRabbitAnti-Mouse)forAbraisedinmiceandPSAR(Peroxidase-conjugatedSwineAntiRabbit)forAbraisedinrabbits. 10)Wash4xwith1xPBScontaining0.01%tween. 11)Addsubstrate(100ul/well). 12)Incubatefor1-5minsinthedarkatRT.Checkreactionforcolourchange.Wellsshouldturnblue. 13)Stopreactionbytheadditionof25ul0.1MH2SO4/well. 14)ReadOD@450nmforTMBSolute 1x 10x NaCl 8g 80g KCl 0.2g 2g Na2PO4(anhydrous) 1.15g 11.5g KH2PO4(anhydrous) 0.2g 2g 1.500ml0.1MSodiumAcetate
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