Team:Washington/Notebook/Standard curve
From 2009.igem.org
(Difference between revisions)
(New page: ====Generating a Standard curve for GFP concentration==== #Purify GFP-fused protein) |
|||
(2 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
+ | __NOTOC__ | ||
+ | {{Template:Team:Washington/Templates/Header}} | ||
+ | |||
====Generating a Standard curve for GFP concentration==== | ====Generating a Standard curve for GFP concentration==== | ||
- | #Purify GFP-fused protein | + | #Purify GFP-fused protein using traditional purification protocol |
+ | #Measure absorption at 280nm to quantify protein amount | ||
+ | #Serially dilute protein into plate and read fluorescence, excitation 485nm, emission 525nm | ||
+ | #Compare values of protein concentration to fluorescence to create a standard curve allowing for the comparison of fluorescence to protein level | ||
+ | |||
+ | {{Template:Team:Washington/Templates/Footer}} |
Latest revision as of 21:36, 18 October 2009
Generating a Standard curve for GFP concentration
- Purify GFP-fused protein using traditional purification protocol
- Measure absorption at 280nm to quantify protein amount
- Serially dilute protein into plate and read fluorescence, excitation 485nm, emission 525nm
- Compare values of protein concentration to fluorescence to create a standard curve allowing for the comparison of fluorescence to protein level