User:Pranav Rathi/Notebook/OT/2013/01/09/DNA-Overstretching Experiments: Difference between revisions
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=Experiments= | =Experiments= | ||
== Experiment 1 (01/04/2013)== | == Experiment 1 (01/04/2013)== | ||
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====Antidig==== | ====Antidig==== | ||
Same for both H2O and D2O since PBS is in H2O only. | |||
20ul of aliquots + 180ul of PBS H2O=200ul of antidig H2O | 20ul of aliquots + 180ul of PBS H2O=200ul of antidig H2O | ||
===Sample preparation=== | ===Sample preparation=== | ||
'''Bead:''' | |||
*H2O: | |||
1.5ul of 265nm bead (1:5) from stock+13.5ul of BGB H2O=15ul of bead H2O (1:5o) | |||
*D2O: | |||
1.5ul of 265nm bead (1:5) from stock+13.5ul of BGB D2O=15ul of bead D2O (1:5o) | |||
'''DNA:''' | |||
ds-DNA 4.4kb (110ng/ml;02/11/11) | |||
*H2O; | |||
1ul of DNA from stock (1:10) + 9ul of 1XPOP H2O =10ul of DNA H2O (1:100) | |||
*D2O; | |||
1ul of DNA from stock (1:10) + 9ul of 1XPOP D2O =10ul of DNA D2O (1:100) | |||
Revision as of 15:32, 14 January 2013
Introduction
This Page contains all the information regarding DNA-Overstretching experiments and results.
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Proof of DNA-tethering
Two video presents good DNA-tethers in H2O and D2O. For some reason D2O tethers look little better. Each moving bead has a ds-DNA tether which is roughly 1500nm long (4.4kb; 110ng/ml; 02/11/11). The bead size is 530nm diameter. This sample is prepared in water and heavy water for DNA-overstretching experiments which i will discuss below. {{#widget:YouTube|id=vKV4CZYMXSw}}{{#widget:YouTube|id=ihl45JssNTA}}
Experiments
Experiment 1 (01/04/2013)
Prepare some new buffers and attempt DNA-tethering in H2O and D2O with 265nm beads (bead radius).
Buffer preparation
BGB is good only for few weeks and it has been over 2 months since i made it last, so i am going to make new BGB and antidig. For more information go to Buffer preparation for DNA overstretching and unzippingexperiments[1]
BGB
- H2O
50mg of BGB + 10ml of H2O 1X POP=5mg/ml BGB 1XPOP H2O 10ml
- D2O
50mg of BGB + 10ml of D2O 1X POP=5mg/ml BGB 1XPOP D2O 10ml
Antidig
Same for both H2O and D2O since PBS is in H2O only.
20ul of aliquots + 180ul of PBS H2O=200ul of antidig H2O
Sample preparation
Bead:
- H2O:
1.5ul of 265nm bead (1:5) from stock+13.5ul of BGB H2O=15ul of bead H2O (1:5o)
- D2O:
1.5ul of 265nm bead (1:5) from stock+13.5ul of BGB D2O=15ul of bead D2O (1:5o)
DNA: ds-DNA 4.4kb (110ng/ml;02/11/11)
- H2O;
1ul of DNA from stock (1:10) + 9ul of 1XPOP H2O =10ul of DNA H2O (1:100)
- D2O;
1ul of DNA from stock (1:10) + 9ul of 1XPOP D2O =10ul of DNA D2O (1:100)