User:Alicia Rasines Mazo/Notebook/CHEM-571 Experimental Biological Chemistry/2014/10/22: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
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|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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==Tasks for October 22==
==Tasks for October 22==
* Data analysis for 30:1 colloid solution vs CaCl2 using MWCO 3500
* Data analysis for 30:1 colloid solution vs CaCl2 using MWCO 3500
* New dialysis of 0.6 g/ L Lysozyme vs KI using 3500 MWCO since dialysis from [http://openwetware.org/wiki/User:Alicia_Rasines_Mazo/Notebook/CHEM-571_Experimental_Biological_Chemistry/2014/10/08 Oct. 8] did not work due to incorrect dilutions
===0.6g/L solution vs KI (MWCO 3500) Dialysis Data===
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<u>Bradford Analysis</u>
*Only running bradford analysis of protein-containing solutions, that is Lys 1, 2, 3, 4 and 5, since the protein cannot diffuse through 3500 MWCO.
* Remove 50 μL of solution from each chamber (7 in all) and run Bradford analysis
**Bradford reagent should be diluted 1:3 with 50mM Tris/50mM NaCl
**Recall, 50 μL solution + 200 μL diluted Bradford + 750 μL Tris/NaCl buffer
**PS cuvettes, measuring 400 - 800 nm
[[Image:Bradford assay 281014.png]]
<u>I- ISE</u>
{| {{table}}
| align="center" style="background:#f0f0f0;"|'''I<sup>-</sup> concentration'''
| align="center" style="background:#f0f0f0;"|'''mV measurement (mV)'''
|-
| 2mM (1) || -175.3
|-
| Lys (1) || -174.0
|-
| 5 mM || -196.4
|-
| Lys (2) || -188.5
|-
| 10 mM || -208.9
|-
| Lys (3) || -210.5
|-
| 25 mM || -231.5
|-
| Lys (4) || -229.1
|-
| 50 mM || -250.2
|-
| Lys (5) || -244.3
|-
|}
<u>UV-Vis measurements</u>
* It was found that KI interferes with the Bradford reagent, so that no Bradford can bind to protein. No peak was seen using UV-Vis
<u>Fluorescence measurements</u>
* No fluorescence measurements were taken on the samples, since nothing was detected using UV-Vis absorption.
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Latest revision as of 00:28, 27 September 2017

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Tasks for October 22

  • Data analysis for 30:1 colloid solution vs CaCl2 using MWCO 3500
  • New dialysis of 0.6 g/ L Lysozyme vs KI using 3500 MWCO since dialysis from Oct. 8 did not work due to incorrect dilutions

0.6g/L solution vs KI (MWCO 3500) Dialysis Data

Bradford Analysis

  • Only running bradford analysis of protein-containing solutions, that is Lys 1, 2, 3, 4 and 5, since the protein cannot diffuse through 3500 MWCO.
  • Remove 50 μL of solution from each chamber (7 in all) and run Bradford analysis
    • Bradford reagent should be diluted 1:3 with 50mM Tris/50mM NaCl
    • Recall, 50 μL solution + 200 μL diluted Bradford + 750 μL Tris/NaCl buffer
    • PS cuvettes, measuring 400 - 800 nm

I- ISE

I- concentration mV measurement (mV)
2mM (1) -175.3
Lys (1) -174.0
5 mM -196.4
Lys (2) -188.5
10 mM -208.9
Lys (3) -210.5
25 mM -231.5
Lys (4) -229.1
50 mM -250.2
Lys (5) -244.3

UV-Vis measurements

  • It was found that KI interferes with the Bradford reagent, so that no Bradford can bind to protein. No peak was seen using UV-Vis

Fluorescence measurements

  • No fluorescence measurements were taken on the samples, since nothing was detected using UV-Vis absorption.