Some finished to do list items 2012

2015-01-13

azim58 - Some finished to do list items 2012



and how to centrifuge and resuspend cells

When I finish doing ELISISPOT/T cell assay testing, return CPV172
pooled peptide to Shen.

Things to do during Christmas break
read the other dissertations (read Hojoon's dissertation first)
make notes about committee meeting
organize and write dissertation
work on mouse tumor cDNA library paper?
fix table 2 of paper
attend to robosep e-mail
https://mail.google.com/mail/u/0/?ui=2&shva=1#label/Career/13b42e7922
bc8194
get more human RNA?
make sure I am on track for graduation
look at graduation details
https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/13ba476b464d1fd3
look at SMC hits
make actual presentation
look over summary document
look over breast cancer grant document
look at other tumor library sequences
meet with Kathy
I'm curious exactly which pools the single clones came from
look at SEREX publication from Kathy
https://mail.google.com/mail/u/0/?ui=2&shva=1#search/compare+and+cont
rast/13b4ce19a56fdfcc
https://mail.google.com/mail/u/0/?ui=2&shva=1#label/Career/13ab9238a5
51fa00
https://mail.google.com/mail/u/0/?ui=2&shva=1#label/Career/13b013bf62
19ea9e
look at travel stuff (e.g. follow up with graduate college travel
grant?)
pJet cloning? (I'm not so sure this is necessary)
reduction to single clone/component.
https://mail.google.com/mail/u/0/?ui=2&shva=1#label/Career/13a4b70fd0
1fdab0
register to vote
https://mail.google.com/mail/u/0/?ui=2&shva=1#label/Miscellaneous/13a
2eaa092393f2a
https://mail.google.com/mail/u/0/?ui=2&shva=1#label/Career/139e2b275e
293817
Automatic DNA microarray gridding based on Support Vector Machines
http://www.researchgate.net/publication/224355444_Automatic_DNA_microarra
y_gridding_based_on_Support_Vector_Machines
Unsupervised SVM-based gridding for DNA microarray images.
http://www.researchgate.net/publication/38057390_Unsupervised_SVM-based_g
ridding_for_DNA_microarray_images
www.midnightclashtiger.deviantart.com
spots, have a membrane for naive, tumor, secondary, and no antibody)

talk to Andrey about poly T in-fusion stop codon issue
L:\storage\Documents\Career\Biodesign Institute\Miscellaneous\Paper
Proofreading for Others\Shen's Dissertation\Chapter 3 of Shen's
thesis\My revisions
check introduction too
Is it okay to have a primer start with many As or Ts? I have a GC clamp
at the end. Here are the primers I want to use.
RPTFC: AAAAAAAAAGCGGCCGCCTAGTAGAACCGTAG
RPTFC2: AAAAAAAAAGCGGCCGCAGAACC

look at clontech 5' end issue
http://www.azim58.wikispaces.net/Entropy+Analysis+of+QC+Samples+7-20-12
surveymonkey.com/s/TNCCCXY
Look at Shen's changes to SMC1fs paper (I think this is all done)
https://mail.google.com/mail/u/0/?shva=1#inbox/1373c21d52f8d86d
o switch axis labels in cross-reactivity figure
discuss how many peptides have with motif are in 108 peptide list

make Kathy's changes to paper
choosing laser power and gain
https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/135ac1b7d2f9317e
https://mail.google.com/mail/u/0/?shva=1#inbox/135ac1b7d2f9317e
see Shen's e-mail from 3-27-12
o respond to Phils e-mail about this
- https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/1371892
6742bf690


https://mail.google.com/mail/u/0/?shva=1#inbox/136a6e76e738a61d
Japan conference
https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/136db7842e8b1b02
o GEO can help me find the relative abundance of transcripts
look at the microarray mRNA data for my particular cell line: 4T1
o Note that Danielle did a lot of this already

3-27-12 e-mail from Stephen
https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/13656cfe6e26cb3b
https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/136418fddd09ccb9
ARCS dinner (April 27th)
Committee Meeting (Thursday April 26th)
3rd floor parts and Lebaer's lab
months FIRE)
see 3-26-12 e-mail from John Phillips
enrollment accepted from Christine Carlson on May 26th
https://mail.google.com/mail/u/0/?ui=2&shva=1#inbox/1369dfe28bcd50af
analyze colony hyb pictures
"S:\Research\Cancer_Eradication\Users\kwhittem\kwhittem\Raw Data Often
Originally on Research Drive\2012\colony hyb 4-3-12"
I also have some images from March 24th
finish entering immunofluorescence protocol
organize Bart's confocal images
"S:\Research\Cancer_Eradication\Users\kwhittem\kwhittem\Raw Data Often
Originally on Research Drive\2012\4-3-12 confocol images"
mailed letter to ARCS donors
write letter to ARCS donors
enter ELISPOT protocol
analyze ELISPOT data
When 2 P50 Biomek tips come in, make sure these are saved for Zbig
analyze SMC1fs data
look at lab manual of Barbas (see 1-5-12 e-mail)
get T cell and phage book
follow up with Topcount and see David Lent's feb 29th e-mail
determine concentration of glycerol stock
make slide-a-lyzer page
perform ELISPOT on T cells from last mouse in old ova group
analyze SMC1fs arrays
analyze decanting results: Test of Decanting after fluor is added 2-3-12
order electrocompetent cells
order 96 well round bottom plates (
http://azim58.wikispaces.com/96+well+round+bottom+plate)
find out amount of reagent used with t cell enrichment kit
If/When cold room is cleared out

read cheek bleed protocol
update protocols learned from Bart
research more info about phage (Dec 1st e-mail from Clontech)
read some of PhD Phage Display Cloning Kit
order SAS
analyze ctl data
analyze array data
Renew Phi Kappa Phi Membership
Check to make sure Sfi site on scFv is compatible with PCANTAB site
34 of 39 on SMART cDNA library kit
Hazardous waste management refresher (Nov 17th e-mail)
Order ELISA plates
edit ARCS application
ask robosep about 4 C
buy more antibodies and dyes
ARCS!
Summary of TED event for JoAnne
monoclonal antibody paper from Stephen (10-30-11)

Deal with Robosep software upgrade (Julia October 21st e-mail)

Find restriction sites outside of SfiI and NotI in PCANTAB
Mark has a a plasmid that can be cut with EcoRI and HindII: pET23a with
gp160