User:Alexander Cvitan/Notebook/Experimental Biological Chemistry Lab/2013/09/24: Difference between revisions

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|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span>
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==Procedure==
==Procedure==
*Note that the hemoglobin had a concentration of 2nm in the pepsin solution.<br.>
*Note that the hemoglobin had a concentration of 20nm in the pepstatin solution. <br.>


==Data==
==Data==
 
*This graph represents the absorbance spectra of each hemoglobin and pepsin or hemoglobin and pepstatin solution at each time interval.
*It is worth noting that it is believed that the pepsin used wasn't active. This is because their wasn't a drastic difference between samples including pepsin and pepstatin.
[[Image:Sept_24_Pep's.png]]
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*Note that all of the samples were normalized by subtracting the signal of the buffer. Also the signals can be compared to the hemoglobin standard.
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Latest revision as of 23:23, 26 September 2017

Biomaterials Design Lab Main project page
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Objective

  • Complete the procedure as outlined by Dr.Hartings here.<br.>
  • Observe activity of pepsin and pepstatin in samples of hemoglobin. <br.>
  • Observe activity using UV-Vis after certain intervals of time.<br.>
  • At each measured interval take a sample of solution and stop the reaction to observe using SDS-PAGE. <br.>

Procedure

  • Note that the hemoglobin had a concentration of 2nm in the pepsin solution.<br.>
  • Note that the hemoglobin had a concentration of 20nm in the pepstatin solution. <br.>

Data

  • This graph represents the absorbance spectra of each hemoglobin and pepsin or hemoglobin and pepstatin solution at each time interval.
  • It is worth noting that it is believed that the pepsin used wasn't active. This is because their wasn't a drastic difference between samples including pepsin and pepstatin.

  • Note that all of the samples were normalized by subtracting the signal of the buffer. Also the signals can be compared to the hemoglobin standard.
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