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Team:Mississippi State/10 June 2008
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(New page: =June 10, 2008= *worked on designing primer #got sequence for lpoA #analyzed for absent restriction sites #looked at map for pPIC6 to look for cloning sites *ran into problems with the k...) |
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| + | {| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center" | ||
| + | !align="center"|[[Team:Mississippi_State|Home]] | ||
| + | !align="center"|[[Team:Mississippi_State/Team|The Team]] | ||
| + | !align="center"|[[Team:Mississippi_State/Project|The Project]] | ||
| + | !align="center"|[[Team:Mississippi_State/Parts|Parts Submitted to the Registry]] | ||
| + | !align="center"|[[Team:Mississippi_State/Modeling|Modeling]] | ||
| + | !align="center"|[[Team:Mississippi_State/Notebook|Notebook]] | ||
| + | |} | ||
*worked on designing primer | *worked on designing primer | ||
Latest revision as of 13:38, 19 June 2008
June 10, 2008
| Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook |
|---|
- worked on designing primer
- got sequence for lpoA
- analyzed for absent restriction sites
- looked at map for pPIC6 to look for cloning sites
- ran into problems with the kit we bought. Invitrogen is ambiguous in their description of vectors. They had no kit w/alpha-factor secretion so we ordered one with E-factor secretion. Turns out there is no signal sequence in the vector (Caleb should be more prudent next time). However, some research has shown it beneficial to use native signal sequence. Hopefully, this will work. Nevertheless, we plan on contacting Invitrogen in the morning to sort mess out.
- Talked to Lee(Dr. Diehl's Lab). He said he will make new cDNA from RNA, then PCR lpoA for us. He plans on starting tomorrow morning and finishing Thurs.
- READ MANUAL FOR PICHIA AND pPIC6!!!!!!!
