User:Mary Mendoza/Notebook/CHEM 571 Experimental Biological Chemistry I/2012/10/16
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| - | * The procedure listed in [[AU Biomaterials Design Lab:Protocols/PCR Mutation Protocol|PCR Mutation protocol]] was strictly followed. After the addition of all reagents, the sample was placed in the thermocycler. | + | * The procedure listed in [[AU Biomaterials Design Lab:Protocols/PCR Mutation Protocol|PCR Mutation protocol]] was strictly followed. After the addition of all reagents, the sample was placed in the thermocycler. |
==Continuation of Chemiluminescence== | ==Continuation of Chemiluminescence== | ||
Revision as of 12:55, 26 October 2012
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PCR mutation
0.46 mg = 0.46E6 ng
Continuation of Chemiluminescence
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=
of primer in water = 4600 μL of water
= 217.39 μL of the dissolved primer in water
×
=
×
=
= 1.20 M of sodium carbonate
= 2.85714 mM of luminol


