Team:BYU Provo/Notebook/Phage Purification/Fallexp/Period1/Exp/9.11CsClGradient

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Bands were visible at the 1.3 level in both tubes. However, in the tube that had more differentiation between steps, the band was very faint. this may be why the band disappeared when a more specific gradient was ran. Now that we know where normal T7 bands, we will be able to extractabove and below the band for small and large mutants.
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Revision as of 20:22, 13 September 2013


Phage Purification September - August Notebook: Experiments



Overview
March-April
May-June
July-August
September-October

9.11 CsCl Gradient


I) Purpose

Try to figure out which density the WT T7 phage bands with our new CsCl stock and new Phage Suspension Buffer.

II) Expected Outcome

We should see a band of WT T7 phage around the 1.2 - 1.5 density.

III) Reagants Used

T7 mutant phage
CsCl
phage suspension buffer


IV) Actual Procedure

Create 2 tubes of different concentrations of CsCl solutions to create a gradient.
For the first tube
Add 0.4225 g of CsCl to 3 mL of phage suspension buffer to create a 1.1 g/ml density gradient.
Add 0.8245 g of CsCl to 3 mL of phage suspension buffer to create a 1.2 g/ml density gradient.
Add 1.2293 g of CsCl to 3 mL of phage suspension buffer to create a 1.3 g/ml density gradient.
Add 1.6371 g of CsCl to 3 mL of phage suspension buffer to create a 1.4 g/ml density gradient.
Add 2.0477 g of CsCl to 3 mL of phage suspension buffer to create a 1.5 g/ml density gradient.
Add 2.4611 g of CsCl to 3 mL of phage suspension buffer to create a 1.6 g/ml density gradient.
Add 2.8774 g of CsCl to 3 mL of phage suspension buffer to create a 1.7 g/ml density gradient.
Add 3.2966 g of CsCl to 3 mL of phage suspension buffer to create a 1.8 g/ml density gradient.
For the second tube
Add 0.5497 g of CsCl to 2 mL of phage suspension buffer to create a 1.2 g/ml density gradient.
Add 0.6844 g of CsCl to 2 mL of phage suspension buffer to create a 1.25 g/ml density gradient.
Add 1.2293 g of CsCl to 3 mL of phage suspension buffer to create a 1.3 g/ml density gradient.
Add 1.4328 g of CsCl to 3 mL of phage suspension buffer to create a 1.35 g/ml density gradient.
Add 1.0914 g of CsCl to 2 mL of phage suspension buffer to create a 1.4 g/ml density gradient.
Add 1.8420 g of CsCl to 3 mL of phage suspension buffer to create a 1.45 g/ml density gradient.
Add 2.0477 g of CsCl to 3 mL of phage suspension buffer to create a 1.5 g/ml density gradient.
Add 1.6407 g of CsCl to 2 mL of phage suspension buffer to create a 1.6 g/ml density gradient.
Add 1.9183 g of CsCl to 2 mL of phage suspension buffer to create a 1.7 g/ml density gradient.
Add 2.1977 g of CsCl to 2 mL of phage suspension buffer to create a 1.8 g/ml density gradient.
Layer the two gradients into two separate centrifuge tubes.
Add 4 mL of mutant phage to the top of the gradient in both tubes
Fill the remaining space in the tube with phage suspension buffer to the top.
Centrifuge at 26500 rpms (100,000 g) for 2.5 hours.

V) Results

Bands were visible at the 1.3 level in both tubes. However, in the tube that had more differentiation between steps, the band was very faint. this may be why the band disappeared when a more specific gradient was ran. Now that we know where normal T7 bands, we will be able to extractabove and below the band for small and large mutants.