Difference between revisions of "User:Samiye Yaman/Notebook/Lab 581/2013/03/20"

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|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Experimental Chemistry</span>
 
|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Experimental Chemistry</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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==Objectives==
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'''Part A: Prepare tris-HCl Buffer'''
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*25mmol/L x 1mol/1000mmmol x 1L/1000mL x 300mL x 121.14g/mol
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= 0.90855g tris
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*Add 250ml of distilled water to the beaker with 0.9094g of tris.
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*Add HCl drop by drop until the pH was at 8.07.
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*47ml of more distilled water was added to have 300ml of 25mM tris-HCl buffer.
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'''Part B: Preparing hydrogels for liposome coating'''
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* 100mg of transfection reagent 1 was dissolved in 5ml choloroform.
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*1 ml of the choloroform with transfection reagent 1 was placed under the hood and let it evaporate. 
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*After the evaporation of the choloroform, 1 ml of phosphate buffer was added to the vial.
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*3 freeze-thaw vortex cycles were applied to the vial in order to create multi lamellar vesicles. (30sec freeze with liquid nitrogen, 30 sec thaw in water bath at room temperature, and vortex for 30sec)
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*By using Nuclepore Track-Etched Membrane, multi lamellar were converted to uni lamellar vesicles.
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*Add 4mg lipid with 2 mg hydrogels.(1. 0.5g PVOH/3mL buffer/6μL R6G/50mL oil 2. 0.5g PVOH/4mL buffer/35mL oil)
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*Gently stir for 2 hours.
  
 
==Description==
 
==Description==
 
   
 
   
*The course is designed by American University to experiment different aspects of PVOH films.
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==Data==
 
 
*During the course PVOH films with different molecular weight will be produced. Effects of cross-linking, addition of different molecules such as gluteraldehyde, different acids, porphrin will be also tested.
 
  
*UV-Vis spectrum, Atomic Absorption spectrum, X-Ray, FTIR, DMA, ISE and many other instruments will be used to analyze the results.
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==Notes==

Latest revision as of 21:34, 26 September 2017

BDLlogo notext lr.png Experimental Chemistry Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png



Objectives

Part A: Prepare tris-HCl Buffer

  • 25mmol/L x 1mol/1000mmmol x 1L/1000mL x 300mL x 121.14g/mol

= 0.90855g tris

  • Add 250ml of distilled water to the beaker with 0.9094g of tris.
  • Add HCl drop by drop until the pH was at 8.07.
  • 47ml of more distilled water was added to have 300ml of 25mM tris-HCl buffer.


Part B: Preparing hydrogels for liposome coating

  • 100mg of transfection reagent 1 was dissolved in 5ml choloroform.
  • 1 ml of the choloroform with transfection reagent 1 was placed under the hood and let it evaporate.
  • After the evaporation of the choloroform, 1 ml of phosphate buffer was added to the vial.
  • 3 freeze-thaw vortex cycles were applied to the vial in order to create multi lamellar vesicles. (30sec freeze with liquid nitrogen, 30 sec thaw in water bath at room temperature, and vortex for 30sec)
  • By using Nuclepore Track-Etched Membrane, multi lamellar were converted to uni lamellar vesicles.
  • Add 4mg lipid with 2 mg hydrogels.(1. 0.5g PVOH/3mL buffer/6μL R6G/50mL oil 2. 0.5g PVOH/4mL buffer/35mL oil)
  • Gently stir for 2 hours.

Description

Data

Notes