User:Wilfred J. Poppinga/Notebook/cAMP compartmentalization/2010/07/10: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
(Autocreate 2010/07/10 Entry for User:Wilfred_J._Poppinga/Notebook/cAMP_compartmentalization)
 
Line 11: Line 11:
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
==Summary==
==Summary==
* Short summary
* Destaining gel remains that was coomassie stained after blotting the cAMP precipitation samples
* Putting the AKAP250 immunoprecipitation samples to gel and blot them
* Gradient (4-12%) SDS-PAGE (NuPage) for cAMP Precipitations
{| border="1"
|+'''Gel loading hTERT D9 + HEK293 & HeLa -S see codes [[User:Wilfred_J._Poppinga/Notebook/cAMP_compartmentalization/2010/06/21|21June2010]]'''
! align="center" style="background:#f0f0f0;"|#
! align="center" style="background:#f0f0f0;"|<u>1</u>
! align="center" style="background:#f0f0f0;"|<u>2</u>
! align="center" style="background:#f0f0f0;"|<u>3</u>
! align="center" style="background:#f0f0f0;"|<u>4</u>
! align="center" style="background:#f0f0f0;"|<u>5</u>
! align="center" style="background:#f0f0f0;"|<u>6</u>
! align="center" style="background:#f0f0f0;"|<u>7</u>
! align="center" style="background:#f0f0f0;"|<u>8</u>
! align="center" style="background:#f0f0f0;"|<u>9</u>
! align="center" style="background:#f0f0f0;"|<u>10</u>
! align="center" style="background:#f0f0f0;"|<u>11</u>
! align="center" style="background:#f0f0f0;"|<u>12</u>
! align="center" style="background:#f0f0f0;"|<u>13</u>
! align="center" style="background:#f0f0f0;"|<u>14</u>
! align="center" style="background:#f0f0f0;"|<u>15</u>
|-
!Gel<br>cAMP prec.
| align="center"|X
| align="center"|X
| align="center"|[[Media:HiMark_protein_marker_-_Invitrogen.jpg|Invitrogen Marker]]<br> (8 μL)
| align="center"|HeLa -S <br>(20 μL)
| align="center"|HEK293<br>(20 μL)
| align="center"|[[Media:Biorad_-_Precision_Plus_Protein_Dual_Color_marker.jpg|Biorad Marker]]<br> (8 μL)
| align="center"|C1<br>(20 μL)
| align="center"|C2<br>(20 μL)
| align="center"|C3<br>(20 μL)   
| align="center"|S1<br>(20 μL)
| align="center"|S2<br>(20 μL)
| align="center"|S3<br>(20 μL)
| align="center"|X
| align="center"|X
| align="center"|X
|-
|}
*After this gel has been blot it will be blocked and then together with the other blot treated with antiAKAP250 antibody
<!--
<!--
==Materials & Methods==
==Materials & Methods==

Revision as of 04:39, 10 July 2010

<html><style type="text/css"> .todo { color: red } .done { color: green} </style></html>

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>

Summary

  • Destaining gel remains that was coomassie stained after blotting the cAMP precipitation samples
  • Putting the AKAP250 immunoprecipitation samples to gel and blot them
  • Gradient (4-12%) SDS-PAGE (NuPage) for cAMP Precipitations
Gel loading hTERT D9 + HEK293 & HeLa -S see codes 21June2010
# 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
Gel
cAMP prec.
X X Invitrogen Marker
(8 μL)
HeLa -S
(20 μL)
HEK293
(20 μL)
Biorad Marker
(8 μL)
C1
(20 μL)
C2
(20 μL)
C3
(20 μL)
S1
(20 μL)
S2
(20 μL)
S3
(20 μL)
X X X
  • After this gel has been blot it will be blocked and then together with the other blot treated with antiAKAP250 antibody