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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: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</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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|style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
 
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<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
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<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->==Adenosine and Inosine UV-Vis and Analysis==
==Entry title==
 
* Insert content here...
 
  
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==Objective==
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*Collect the data on the UV-Vis from the ionisine dilutions
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The inosine samples came from [[User:Megan_L._Channell/Notebook/Horseradish/2013/09/03 | yesterday's]] protocol
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*Calculate calibration curves for Adenosine and Inosine
 +
*Run a data regressions on the class' data
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==Protocol==
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Yesterday, our adenosine dilutions were much lower than the class' average, so we redid the adenosine samples.  A new stock solutions was made using [[User:Megan_L._Channell/Notebook/Horseradish/2013/09/03 | yesterday's]] protocol and the stock solutions was made from .0809g of adenosine.
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[[Image:Adenosine2 9 4 2013 cmj.jpg]]
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==Data==
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A UV-Vis spectra of the new adenosine samples and the inosine samples were collected.  The parameters for the UV-Vis were measured between 450 and 200nm.  The peak for the insonie spectra was at 249nm while the adenosine was 259nm.  This wavelength was used when calculating the calibration curve.
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[[Image:Inosine 9 4 2013 cmj UVVIS.jpg]]
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[[Image:Inosine 9 4 2013 cmj cali.jpg]]
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[[Image:Adenonsinefixedtrial2 9 4 2013 cmj.png]]
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[[Image:Adenosinetrial2 9 4 2013 conc.jpg]]
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==Data==
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[[Image:Adenosine 9 4 2013 cmj trial2 grubbs.png]]
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[[Image:Inosine 9 4 2013 cmj grubbs.png|1050px]]
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*The Grubbs test was calculated using the formula
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G=|mean-x|÷std. dev.
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*The data that our group collected from 9/3/2013 was lower.  We remade Adenosine concentrations from a new stock solution, but did not do that for inosine, thus our group (5) data is not recorded.
  
 
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Latest revision as of 22:17, 26 September 2017

BDLlogo notext lr.png Biomaterials Design Lab Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png

Adenosine and Inosine UV-Vis and Analysis

Objective

  • Collect the data on the UV-Vis from the ionisine dilutions

The inosine samples came from yesterday's protocol

  • Calculate calibration curves for Adenosine and Inosine
  • Run a data regressions on the class' data

Protocol

Yesterday, our adenosine dilutions were much lower than the class' average, so we redid the adenosine samples. A new stock solutions was made using yesterday's protocol and the stock solutions was made from .0809g of adenosine.

Adenosine2 9 4 2013 cmj.jpg

Data

A UV-Vis spectra of the new adenosine samples and the inosine samples were collected. The parameters for the UV-Vis were measured between 450 and 200nm. The peak for the insonie spectra was at 249nm while the adenosine was 259nm. This wavelength was used when calculating the calibration curve.

Inosine 9 4 2013 cmj UVVIS.jpg Inosine 9 4 2013 cmj cali.jpg Adenonsinefixedtrial2 9 4 2013 cmj.png


Adenosinetrial2 9 4 2013 conc.jpg

Data

Adenosine 9 4 2013 cmj trial2 grubbs.png Inosine 9 4 2013 cmj grubbs.png

  • The Grubbs test was calculated using the formula

G=|mean-x|÷std. dev.

  • The data that our group collected from 9/3/2013 was lower. We remade Adenosine concentrations from a new stock solution, but did not do that for inosine, thus our group (5) data is not recorded.