User:Matt Hartings/Notebook/Photosynthesis/2013/01/18: Difference between revisions
From OpenWetWare
(Autocreate 2013/01/18 Entry for User:Matt_Hartings/Notebook/Photosynthesis) |
No edit summary |
||
Line 11: | Line 11: | ||
==Objective== | ==Objective== | ||
Measure stock DNA solutions | |||
==Procedure== | |||
Dilute samples (2 uL of DNA, 198 uL of water) | |||
Measure absorbance. | |||
Assume: for dsDNA, an absorbance of 1 corresponds to a concentration of 50ug/mL and for oligos an absorbance of 1 corresponds to a concentration of 20ug/mL | |||
When I could, I used data sheets from IDT for epsilon values of oligos | |||
==Data== | |||
[[Image:20130118_DNA_UVVis.png|400px]] | |||
Important notes: | |||
# I need to do new mini/midi-preps for WT sw Mb and pQE-80 as the concentrations were just so low. | |||
# Asc Hb T109C f 136ug/mL (from assumption) | |||
# Asc Hb T109C r 272ug/mL (from assumption) | |||
# sw Mb M131T f 60.5 mmol/mL (from data sheet) | |||
# sw Mb M131T r 10.3 mmol/mL (from data sheet) | |||
# sw Mb pQE80 clone f 95.1 mmol/mL (from data sheet) | |||
# sw Mb pQE80 clone r 30.4 mmol/mL (from data sheet) | |||
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### --> | <!-- ##### DO NOT edit below this line unless you know what you are doing. ##### --> |
Revision as of 12:32, 18 January 2013
Protein Re-engineering | <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page <html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html> </html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html> |
ObjectiveMeasure stock DNA solutions ProcedureDilute samples (2 uL of DNA, 198 uL of water) Measure absorbance. Assume: for dsDNA, an absorbance of 1 corresponds to a concentration of 50ug/mL and for oligos an absorbance of 1 corresponds to a concentration of 20ug/mL When I could, I used data sheets from IDT for epsilon values of oligos DataImportant notes:
|