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ELISA (EnzymeLinked ImmunoadSorbent Assay)
ELISA(Enzyme-LinkedImmunoadSorbentAssay)
Youwillneedthefollowingsolutions:PBS(Phosphate-BufferedSaline,Ca/Mgfree):-
Solute | 1x | 10x |
---|---|---|
NaCl | 8g | 80g |
KCl | 0.2g | 2g |
Na2PO4(anhydrous) | 1.15g | 11.5g |
KH2PO4(anhydrous) | 0.2g | 2g |
N.B.:Na2HPO4.2H2Ocanalsobeused->add1.42gfor1xand14.2gfor10xPBS.Makeupto1litrewithddH2O.
PBSwash:-
100ml1xPBS10ulTween(0.01%,finalconcentration)
Citrate/AcetateBufferpH6.0:-
- 1.500ml0.1MSodiumAcetate
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@450nmforTMB.
ELISA相关仪器试剂设备
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