Today's To Do's
- SDM cd79b-ptet:mrfp-gal4vp16
- Innoculate Midi TRE:gal4VP16
- Transform:
- pENTR LacI and pENTR pLac
- Miniprep, digest, gel
- TRE:Syk-pTet:mRFP-TEVp
- pLac:mKate
- TRE:gal4vp16 #2 (should be in unverfied mini/midi in 4C) - see cloning progress 06/26
- rerun digest/gel from yesterday (TRE:gal4vp16 with XhoI, TRE:mKate and hEF1a:LacI LR1 #2,3 with SalI and ApaI resp.)
- LR hef1a:cymR and hEF1aCuO:mkate (look to see if CMV5CuO is in lab promoter box - report number to Brian)
- Split HEK293
CMV5-CuO 715:
hEF1a-CuO 715:09
CymR-CuO 710:09
Geneious To Do List:
SDM primers: CD79B, Gal4VP16, TEVp
- TRE:gal4vp16 sequencing primers
- TRE:Syk-mRFP-(t)TEVp sequening primers - Kathryn
hef1a sequencing primers
^^^Email: bcrpeeps@mit.edu
^^^Pass: grapefruit
Higher Level To Do's:
- Decide on other antigen-variable regions we want to test
- Other experimental planning (on experimental page)
- Parts list (excel sheet detailing specs/locations of parts)
- How do we do site directed mutagenesis?
- Literature research:
- kozak sequences for heavy and light chains and CD79s
- truncated TEVp
- other antigens to detect using BCR (we were thinking of small molecule detection)
- inducible promoters (we were considering LacI - an inducible repressor - but we want to look into other options first)
- Cloning planning
- hEF1a:Syk-pTet:mRFP-TEVp
- variable region