User:Jamie Nunziata/Notebook/Protease Research/2015/10/13: 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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==Procedure==
==Procedure==


7 samples of AuNP fibers were spun down at 300rpm for 10 minutes.These fibers will be used for our 120min, 90min, 60min, 45min, 30min, 15min, and 10min samples. 21.0µL of 47.656µM a-chymotrypsin (in Tris) and 979.0µL of Tris buffer was added to each sample tube and a blank Eppindorf tube (no fibers), making the final solution 1µM a-chymotrypsin.
7 samples of AuNP fibers were spun down at 300rpm for 10 minutes.These fibers will be used for our 120min, 90min, 60min, 45min, 30min, 15min, and 10min samples. 21.0µL of 47.656µM a-chymotrypsin (in phosphate buffer) and 979.0µL of phosphate buffer was added to each sample tube and a blank Eppindorf tube (no fibers), making the final solution 1µM a-chymotrypsin.




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A full lab procedure can be found in Nicole Bonan's notebook entry for [[User:Nicole_Bonan/Notebook/Chem_571_Lab_Notebook/2015/09/13|today]]
A full lab procedure can be found in Nicole Bonan's notebook entry for [[User:Nicole_Bonan/Notebook/Chem_571_Lab_Notebook/2015/09/13|today]]


 
Fluorescence for each sample was measured between the emission spectrum from 400 to 600nm, and the data is recorded below
Absorbance for each cuvette was measure via UV-Vis between the emission sprectrum of 400-800nm, and the data is recorded below
 


==Data==
==Data==

Latest revision as of 01:21, 27 September 2017

Project name Main project page
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Objective

The objective of today's lab was to use a Fluorescence Assay to determine the rate a 1µM solution of a-chymotrypsin degrades AuNP fiber samples.

Procedure

7 samples of AuNP fibers were spun down at 300rpm for 10 minutes.These fibers will be used for our 120min, 90min, 60min, 45min, 30min, 15min, and 10min samples. 21.0µL of 47.656µM a-chymotrypsin (in phosphate buffer) and 979.0µL of phosphate buffer was added to each sample tube and a blank Eppindorf tube (no fibers), making the final solution 1µM a-chymotrypsin.


To each cuvette, the following was added:

  • 20uL of the blank or sample
  • 140uL of Assay Buffer
  • 40uL of Assay Reagent

A full lab procedure can be found in Nicole Bonan's notebook entry for today

Fluorescence for each sample was measured between the emission spectrum from 400 to 600nm, and the data is recorded below

Data



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