User:Tamanika Tinsley/Notebook/Chem 581 Biomaterials Design Lab/2014/10/08: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
Line 9: Line 9:
*Group Members Andrew Farag Sr (Undergrad) and Michael Bible Jr (Undergrad)  
*Group Members Andrew Farag Sr (Undergrad) and Michael Bible Jr (Undergrad)  
*Group Name : AMT
*Group Name : AMT
==Objective==
==Objective==
*To make stock solutions  
*To make stock solutions  

Revision as of 12:35, 17 October 2014

Project name <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Oct 8 - Fluorescence

  • Group Members Andrew Farag Sr (Undergrad) and Michael Bible Jr (Undergrad)
  • Group Name : AMT

Objective

  • To make stock solutions
  • To take UV-Vis and Fluorescence spectra of prepared R6G samples
  • To make a calibration curve using both fluorescence and UV-Vis data
  • To finish film synthesis

Notes

The completion of the film synthesis used the procedure from Tami's Notebook

R6G Fluorescence: Calibration and Measurement Completed by Michael

  1. Make stock concentrations (both groups can use the same solutions)
    • Initial stock: 2500μM, secondary stock: 500μM
    • 0.10μM
      • Made with 500μM solution
    • 0.50μM
      • Made with 500μM solution
    • 1.0μM
      • Made with 500uM solution
    • 1.5uM
      • Made with 500μM solution
    • 2.0μM
      • Made with 2500μM solution
    • 0.75μM
      • Made with 500μM solution
    • 1.2μM
      • Made with 500μM solution

Thanks to Madeleine for making initial 2500μM solution of R6G.

Fluorimeter Settings

  • 500nm excitation
  • 515-700nm scan range
  • 10.0nm slit width
  • 200nm/min scan speed