User:Jacob Esenther/Notebook/Chem 571/2014/10/14: Difference between revisions
From OpenWetWare
(fix raw html notebook nav) |
|||
(3 intermediate revisions by one other user not shown) | |||
Line 2: | Line 2: | ||
|- | |- | ||
|style="background-color: #EEE"|[[Image:BDLlogo_notext_lr.png|128px]]<span style="font-size:22px;"> Biomaterials Design Lab</span> | |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"| | |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]] }}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}} | ||
|- | |- | ||
| colspan="2"| | | colspan="2"| | ||
Line 15: | Line 15: | ||
==Description== | ==Description== | ||
# Extracted contents of the HCl Lysozyme dialysis | # Extracted contents of the HCl Lysozyme dialysis | ||
## These were placed into 1.5mL centrifuge tubes for further testing | |||
# Ran titrations | # Ran titrations | ||
## Michael preformed the titrations | |||
## The procedure may be viewed on Dr.Fox's page [[User:Douglas_M._Fox/Notebook/AU_CHEM-571_F2011_Lab_Support/2014/10/08|here]]. | |||
# Created new SDS Page Solutions | # Created new SDS Page Solutions | ||
## Mixed 10 μL 0.6 g/L lysozyme with 10μL SDS-PAGE sample buffer in 1.5 mL centrifuge vial | |||
## Mixed 10 μL 0.12 g/L lysozyme with 10μL SDS-PAGE sample buffer in 1.5 mL centrifuge vial | |||
## Mixed 10 μL 30:1 Au/lysozyme colloid with 10μL SDS-PAGE sample buffer in 1.5 mL centrifuge vial | |||
## Mixed 10 μL 0.12 g/L unknown protein with 10 μL SDS-PAGE sample buffer in 1.5 mL centrifuge vial | |||
## Placed in heating block (set at 90 °C) for 5 minutes | |||
## Stored in refrigerator overnight | |||
# Created a Potassium Phosphate Buffer | # Created a Potassium Phosphate Buffer | ||
## The original protocol asked to make the buffer using KH<sub>2</sub>PO<sub>4</sub> and 1M KOH | |||
## We opted to use the monobasic and dibasic species of the molecule to obtain the desired pH of 6.24 | |||
##* Calculations for the buffer were made using this website [[http://www.liv.ac.uk/buffers/buffercalc.html|The University of Liverpool Buffer Calculator]] | |||
==Data== | ==Data== | ||
* | To make the Potassium Phosphate buffer we used: | ||
* 0.0839g of K<sub>2</sub>HPO<sub>4</sub> | |||
* 0.2888g of KHPO<sub>4</sub> | |||
==Notes== | ==Notes== |
Latest revision as of 00:26, 27 September 2017
Biomaterials Design Lab | Main project page Previous entry Next entry |
ObjectiveLearn how to maintain an OpenWetWare Notebook. Description
DataTo make the Potassium Phosphate buffer we used:
NotesThis area is for any observations or conclusions that you would like to note.
|