User:Elizabeth Ghias/Notebook/Experimental Chemistry/2013/04/19: Difference between revisions

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|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Experimental Chemistry</span>
|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Experimental Chemistry</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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unknown [DNA]/A<sub>260</sub> = 50 ug/ml/1.0  
unknown [DNA]/A<sub>260</sub> = 50 ug/ml/1.0  
# Took a UV-vis measurement of the DNA by putting 2 uL of DNA and 198 uL water in a small volume cuvette
# Plotted the data and found the absorbance at 260 nm
# Solved the above equation and found the concentration of DNA to be 1610 ug/mL
# Then figured out the volume of DNA stock that contains 200 ng → there are 200 ng in 0.124224 uL.  Therefore, we will add 1 uL of DNA to each sample
<u>Tris Buffer Preparation</u>
* A 50 mM tris buffer with a pH of 7.6 was prepared by


==Data==
==Data==

Latest revision as of 22:40, 26 September 2017

Experimental Chemistry Main project page
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Objective

To prepare a tris buffer for the DNase activity testing and to determine the concentration of DNA in the DNA stock to be used for activity testing.

Description

Determining the Concentration of the DNA stock

  • We want to add 200 ng DNA to each sample for activity testing.
  • the absorbance and concentration of DNA are linearly related according to the equation:

unknown [DNA]/A260 = 50 ug/ml/1.0

  1. Took a UV-vis measurement of the DNA by putting 2 uL of DNA and 198 uL water in a small volume cuvette
  2. Plotted the data and found the absorbance at 260 nm
  3. Solved the above equation and found the concentration of DNA to be 1610 ug/mL
  4. Then figured out the volume of DNA stock that contains 200 ng → there are 200 ng in 0.124224 uL. Therefore, we will add 1 uL of DNA to each sample

Tris Buffer Preparation

  • A 50 mM tris buffer with a pH of 7.6 was prepared by

Data

  • Add data and results here...

Notes

This area is for any observations or conclusions that you would like to note.


Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.



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