User Manual
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3.7 Comb Specications for (GC)MGU-502T and (GC)MGU-602T
SECTION 4
Running Conditions
4.1 Recommended Power
Therecommendedpowerconditionsforoptimalresolutionare50to150V,constant,
and25to80mA.Theusualruntimewillvaryforthevoltagechosenbutshould
rangefrom15to60minutes,monitoringnucleicacidmigrationbyprogressofmarker
dyes.Constantpowerisnotanecessity,butitproducesuniformheatthroughoutthe
run.Besurethepolarityiscorrecti.e.thattheDNAisloadednearthecathode(black
electrode)toruntowardtheanode(redterminal).
4.2 Recommended Buffers
Type ConcentratedStock/liter FinalConcentration
TAE 50X-242gmTrisbase 1X-0.04MTris-acetate
(Tris-acetate) 57.1mlglacialaceticacid 0.001MEDTA
100ml0.5MEDTA(pH8.0)
TBE 5X-54gmTrisbase 0.5X-0.045MTris-borate
(Tris-borate) 27.5gmboricacid 0.001MEDTA
20ml0.5MEDTA(pH8.0)
10X-LoadingBuffer(DNA)
0.25%Bromophenolblue
0.25%Xylenecyanol
20%FicollType400
0.1MEDTA,pH8.0
4.3 References
1)Hames,B.D.,Rickwoood,D.(ed.)(1990).GelElectrophoresisofNucleicAcids.A
PracticalApproach.2ndedn.IRLPress,Oxford.Ch2.
2)Sambrook,J.,Fritsch,E.F.,Maniatis,T.(1989).MolecularCloning.ALaboratory
Manual.2ndedn.ColdSpringHarborLaboratoryPress,ColdSpringHarbor,New
York.Ch6.
3)Ausubel,F.M.,Brent,R.,Kingston,R.E.,Moore,D.D.,Seidman,J.G.,Smith,J.A.,
Struhl,K.(ed)(1993).CurrentProtocolsinMolecularBiology.Vol.1,GreenePublish-
ingAssociates,Inc.andJohnWiley&Sons,Inc.,Ch.2.