Alberta/Calender/September

From 2007.igem.org

< Alberta | Calender(Difference between revisions)
(→September 27)
(→September 27)
 
(30 intermediate revisions not shown)
Line 202: Line 202:
<b>To Do:</b><br>
<b>To Do:</b><br>
Ligations<br>
Ligations<br>
 +
 +
 +
<b>Lab Notes:</b><br>
 +
Transformed BB Boo DB and BE Boo DB and plated onto Amp plates. (In 37 deg)
 +
 +
Started overnights of R0080 from picked colonies, used Amp. (In shaker)
 +
 +
Restreaked I0500 for single colonies on plates. (Left at 37 deg)
 +
 +
 +
<B> Goodies will be served during the meeting (7:00pm @ CAB 373), so be sure to show up! </b>
<B> Goodies will be served during the meeting (7:00pm @ CAB 373), so be sure to show up! </b>
Line 461: Line 472:
AL - 12-2pm
AL - 12-2pm
 +
 +
<b>Lab Notes:</b><br>
 +
Mini preped DBEBB and DBBBE, 4 overnights each.
 +
Made glycerol stocks of overnights (in -80 deg)
NK-6PM
NK-6PM
 +
 +
<b>Lab Notes:</b><br>
 +
Restrict DBEBB and DBBBE with XBA and PST, and SPE and PST.
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 484: Line 502:
ED- 6PM  
ED- 6PM  
 +
<b>Lab Notes:</b><br>
 +
 +
Picked up I0500 from Mike and plated on KAN plates.
 +
 +
Made a gel with EtBr in the gel.
 +
 +
Ran a gel of the digests that occurred on September 18th.
 +
 +
Took picture of gel for analysis tomorrow.
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 495: Line 522:
JP- late
JP- late
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Picked single colonies from growth on I0500 plates and made overnights and replated on kan plates.
 +
 +
Restrictions on DBBEBB and DBBBE are restarted, XPA and PST, SPE and PST.
 +
 +
Sequencing reactions of Buddy, Betty, Benny, Enny and DB.
 +
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 508: Line 544:
CZ-2:15PM <br>  
CZ-2:15PM <br>  
ED - 4 PM
ED - 4 PM
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Restricted I0500 with ECO and XBA.
 +
 +
Ran a gel of digested I0500.
 +
 +
Took a picture of gel for analysis in the following lab day.
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 521: Line 565:
JP evening
JP evening
 +
<b>Lab Notes:</b><br>
 +
 +
Digested J61003 with ECO and XBA.
 +
 +
Digested I0500 with ECO and SPE.
 +
 +
Made a gel and ran the restrictions described above.
 +
 +
Gel Extracted J61003 band from the gel. (Stored in -20 deg)
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 534: Line 587:
NK 230-530
NK 230-530
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Repeat digestion of I0500 with 16 microlitres this time.
 +
 +
Ran on a gel, but did not provide a good picture and discarded.
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 546: Line 605:
PM - NK @5 <br>
PM - NK @5 <br>
sorry, cant make it till 630
sorry, cant make it till 630
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Started overdays of I0500 picked colonies. (Left in shaker at 37 deg)
 +
 +
Did a mini prep on I0500, followed protocols in Fermentas Kit
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
== September 25 ==
== September 25 ==
 +
930-1230 NK
930-1230 NK
 +
 +
1-ish - AL
2pm-ish - VH
2pm-ish - VH
 +
 +
TO DO LIST:
 +
 +
1)
 +
 +
looking through the book to last thursday at my sequencing reactions and figure out exactly what samples I used for X-2, X-3, and X-4?
 +
 +
2)
 +
 +
If there is not much left (less than 20 microL), can you transform into bacteria so we can complete another mini? (only 1 transformation for each)
 +
 +
3)
 +
 +
place each of those tubes in a rack or something and leave directions so wayne can find it.
 +
 +
4)
 +
 +
X-1 has two prefixes, so its garbage, but X-5 might be ok. I couldn't find a terminator or a suffix. So... Can you complete a restriction on X-5 with Eco/Spe and Eco/Pst and run on a gel to make sure it cuts properly (and therefore those restriction sites exist)
 +
 +
5)
 +
 +
run sequencing reaction on more X-1 and X-5's (look at the chart erin made from back in the day - its a fold out piece of paper in the master book)
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Digest I0500 with ECO and SPE - only half completed because ran out of SPE.
 +
 +
Line 559: Line 655:
== September 26 ==
== September 26 ==
 +
ML
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Completed digests from yesterday that could not be finished due to a lack of SPE.
 +
 +
Ran a gel of products of digest but did not yield a good picture and gel was discarded.
Line 569: Line 672:
JP- evening
JP- evening
 +
 +
<b>Lab Notes:</b><br>
 +
 +
Redid overnights of I0500 so that they can be Re-minid.
 +
 +
Ran a new gel of the previous minid I0500s to see what is wrong with them. Result shows that there is not enough DNA for these samples to be usefull.
 +
 +
Started PCR for Thiolase.
 +
 +
Made overnights of Buddy in B0034 using the glycerol stocks.
 +
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
Line 574: Line 688:
JG & MC - 8:00AM <br>
JG & MC - 8:00AM <br>
-
CZ 2:30pm
+
1-ish - AL
 +
 
 +
CZ 2:30pm<br>
 +
Redid miniprep of I0500 induced by IPTG(1C,1D,2C)and elute in 40 microlitre<br>
 +
Ran 3microliter ona gel but nothing appeared<br>
 +
Miniprep discarded because of lack of DNA<br>
 +
James took 1D culture ands ub culture and perhaps induce with IPTH again.<br>
 +
Restarted 1C and 2C (5ml LB, 5microlitre K, 100microlitre culture)<br><br>
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
== September 29 ==
== September 29 ==
-
CZ 2:00 pm
+
ED 9:00 am<br>
 +
Made of gel of James's Miniprep digests<br>
 +
Digest I0500 with ECORI and SPE<br>
 +
Transformations of Ligations Enny + J61003 and Betty + J61003<br>
 +
 
 +
NK 1130-230<br>
 +
Loaded gel but samples were incorrectly loaded<br><br>
 +
CZ 2:00 pm<br>
 +
Loaded gel of Erin's digests<br>
 +
Gel extraction<br>
 +
Ligation with J61003 E, X<br>
 +
 
 +
Note:The new TAE is taking much longer to solidify when 1%. <br>
 +
 
 +
JP evening<br>
 +
Tholase PCR<br>
 +
Sequencing reactions of DB in Boo and Buddy in Boo<br>
-
JP evening
 
[[Alberta/Calender/September#September|to the top]]
[[Alberta/Calender/September#September|to the top]]
== September 30 ==
== September 30 ==
 +
ED 9:00 Am<br>
 +
Transformed Buddy+J61003, I0500+J61003 #1 and #2<br>
 +
Plated all cells on AMP<br>
 +
O/Ns of Enny+J61003 and Benny+J61003<br>
 +
NG 12:00 am<br>
 +
 +
JP<br>
 +
Tholase blunt end  topo reaction<br>
 +
Completed reaction and tholase mix is in orange PCR tube rack at -20<br>
 +
Note:<br>
 +
1) We need XGAL!!<br>
 +
2) Colonies that are blue do not have thiolase in them, colonies that are wight do have thiolase in them.

Latest revision as of 23:33, 24 October 2007

Contents

September

September 2007
Su M Tu W Th F Sa
1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18 19 20 21 22
23 24 25 26 27 28 29
30


To August 2007
To October 2007
Back to UofA iGEM Home

September 1


Lab Notes
1. 24 Minipreps for Diezel Blaze in B0034 using Fermentas Kit; stored in -20 freezer
2. Lots of colonies from the transformation last night; no colonies on negation control (good) and lots of colonies on positive control (good) and no satellite colonies (also good); no colonies were picked for overnights
3. Run the Buddy+Benny in B00 and Betty+Enny in B00 Pst/Xba gel from last night at 50V for another 30 minutes for better resolution; all the digest worked so I cut out the appropriate bands and stored the gel in -20 freezer for purification later

-CZ


to the top

September 2

to the top

September 3

to the top

September 4

Schedule:

JP,ML,JG 7:00pm


For the record:
Buddy = BuOH DH 1235 bp
Betty = Bb-bhBu-coa dh 923 bp
Benny = Butyryl coa dh 1184 bp
enny = Enoyl coa Hydratase 860 bp
Diezel Blaze = buAld-Dh 2639 bp

Notes:
Moving was done this mid-day.
New location M349
JG has key & access
- MC, ED, JG

Evening crew - please do a once over of G308 to double check we have not left anything and to clean up anything extra/ things we should get out of the way. thnx - MC

Night Crew

-JP, JG

Set up new lab

Things we need - Water Bath, Scale, disposable 13ml overnight tubes, Tip waste

lab work

Gel purification ran on Betty,enny and boo as well as buddy and benny and is in the -20 in the new lab

To Do list for tomorrow

- Restriction on DB needs to be done - If we want to put it in front of BE or BB then Spe/Pst - If we want to put it behind BE or BB then cut with Xba/Pst - maybe do both (use 4microL DNA for digest)

-complete restriction on BE and BB for SPE and PST (then we can complete ligations BE-BB and BB-BE or we can ligate D.B into BE or BB to make BE-DB or DB-BE or BB-DB or DB-BB- Then we can ligate BE-BB-DB or DB-BE-BB or BE-BB-DB or BB-DB-BE or BB-BE-DB and we are kinda finished!

- If I0500 comes in from calgary it needs to be transformed.

- Transform R0080 which is a back up promoter just in case?


-Note we also have to do sequenceing on BB and BE and DB

Shout out to calgary for saving our necks Shout out to the move in crew to the top

September 5

Schedule:

NG,ED,ML 7:00pm

AM Crew Notes:

finished up cleaning up post-move in
got a 'water bath' - JG calibrated it
prepared BB in Boo & BE in Boo for sequencing - this will be ready for pick up tomorrow
Restricted:
- DB in BOO with PST/XBA
- DB in BOO with PST/SPE
- BB in BOO with PST/SPE
- BE in BOO with PST/SPE
NB: there is a section in the masterbook "figuring stuff out" just a few questions I have from being away so long - don't worry about it we should do a wet lab recap to bring everyone on the same page at our meeting Thrusday - MC
<3 JG & MC

Transformed I0500 from Calgary. Transformed R0080. Ran digestions on gel. Ligated digested DB with BB and BE. (all in Boo)

-ED, ML


to the top

September 6

Schedule:

NK ED AL 5:00pm (Unless your crazy enough to show up at 5AM)

To Do:
Ligations


Lab Notes:
Transformed BB Boo DB and BE Boo DB and plated onto Amp plates. (In 37 deg)

Started overnights of R0080 from picked colonies, used Amp. (In shaker)

Restreaked I0500 for single colonies on plates. (Left at 37 deg)



Goodies will be served during the meeting (7:00pm @ CAB 373), so be sure to show up!

to the top

September 7

Schedule:

AM Crew: MC, JG meeting at 800hrs

Lab Notes:
No growth observed for R0080 overnights; just scrapping it because we have I0500
No growth on transformations of BB+DB and BE+DB ligations therefore . . . religated - see masterbook for more details
O/N with AMP for I0500
Transform religations in to XL10 Gold
-MC, JG, ML

NB: JG has key access

To Do:
Mini preps on I0500 overnights


to the top

September 8

Schedule:

Super Awesome Marathon of Productiveness

8-11: JG,NG
Miniprep I0500
DB BE and DB-BB transformations did not work.
Re-ligated DB into BB boo and DB into BE boo


11-2: AL,ML
Re-transform BE+DB and BB+DB

2-5: VH
Gel extraction of I0500, but we missed the step "restricting with Ecori+speI"

5-8: JP,NK
Restrction on I0500 mini's with Ecori and SPeI


to the top

September 9

Schedule:

And Yet another super productive Sunday

8-11: NG and CZ

NG - Nobody Called me about the key last night (and I completely forgot to swing by: was with parents). So I will wait by the lab either , until the next group shows up or someone with a key. Also bioSci is locked but there is an open door by the physcology wing. I have my cell on 902-8032.

NG - Update: 9:30am 'broke' into lab :D. Then found key...

11-2: VH, CZ
Nick ran the gel of I0500 restricited by Eco/Spe, but nothing showed up as expected (1.5kb).
Digested I0500 and J61003 with Eco/Pst as instructed.

2-5: MC, JG
ran gel of restricted I0500 & J61003; unfortunately there is no DNA in the I0500 sample either
gel extracted J61003
Made LB - to be divided into bottles & autoclaved in G308
O/N of DB in BB & DB in BE samples left in 37degree room

5-8: ML, ED autoclaved little bottles of LB. NOTE: does not need to be autoclaved before you pour it into little bottles and then re-autoclave. Just pour into bottles and autoclave once digested all in Boos except for DB with Pst/xba

to the top

September 10

Schedule: And Scheduling just got hard core

I have sheduled what we have taken down in the meeting some people appear many times on this schedule working alone just because of the time they were availible. If you are comfortable working alone and taking on lots of shifts im sure the team would be greatful but I'm also sure we would also understand if you didn't want to work alone in the lab. I have only scheduled this way because we need man hours so i tried to fill up all the spots as best i could. -JG

MC,JG for the AM
put away bottled LB
Ran gel of last night's restricted samples "in boo"; did not really turn out
ran gel of uncut & single restricted I0500; uncut I0500 showed 2 bands and restricted showed nothing
Mini prepped Ligations of DB in BB and DB in BE

to do: - run gel of double digested I0500
- do single & double restriction on Mini prep of Ligations
- run gel of uncut, single & double restrictions of mini prepped ligations

ML,AL for the MID (AM crew: What time will you guys be at the lab till? I won't be there until 12:30. Might need to arrange something in order to pick up keys. - AL)
Double digest of BB-DB/BE-DB XBA/PST

NG (2:30-4) for the PM (celine is in calgary if you dont feel comfortable in the lab by yourself I can show up - JG) Jason if you have time to show up that would be sweet, but if you don't I understand. -NG
Ran gel of the restrictions made in MID, Sept 10 by ML and AL.


JP,ED for the Night


to the top

September 11

Schedule: No one else really signed up for tuesdays so anyone who has time to drop in should

AM- NK Restrictions of BB+DB with XBA/PST and BE+DB with PST, SPE

Mid - AL (12:30 - 2 ish), NG (random)
Ran gel on restrictions made by NK in AM of Sept 11

Night- ED JP
Gel extractions
Ligations of DB+BB + BE and DB+BE + BB
mini relocation 1 bench back, do not use the first 3 benches of the lab or the blackboard from now on!

to the top

September 12

Schedule:

NG Hi guys I have a meeting 3:30 that cannot be reseached I moved myself to come in Tuesday instead (when nobody was in).

AM -

Mid- ML, AL

Important: Please evacuate lab before 2:00pm as there is a lab class starting at this time till 5pm! -AL

PM - VH
lab class 2-5 VH: please make note of the above announcement regarding lab class at 2:00pm

Night - CZ, ED
Transformed BEDBB and BBDB into XL 10 gold

to the top

September 13

Schedule:

AM-Nik

Digested BEBOO and BBBOO with PST and XBA

PM - VH, JG
Ran gel of restrictions made in the previous shift.

Meeting 7:00

After lab shift, JG, JP
Overnights with AMP of BBDB + BEDB
Gel extractions from gel made in the prevous shift
bands 1,2 (BE) correct while band 3 is too large to be BB
Sequence reactions can now be started using primers 1-5 that have been diluted to 5pmol/microlitre in H20 not TE

to the top

September 14

Schedule:

AM - MC (around 900/930hrs)
- Mini prep from O/N of BBDBE & BEDBB
- Glycerol stocks of BBDBE & BEDBB, and restreaked quartered plates
- Gel extraction of BE & BB Xba/Pst
- made gel

Mid - AL, JG
Restrictions on BBDBE and BEDBB with xba/pst and spe/pst
PM - VH, CZ
Ran gel on restrictions on BBDBE and BEDBB with xba/pst and spe/pst
Gel extracions

night - JP
Sequencing reactions
BBDBBE 6 reactions
BEDBBB 6 reactions
BB 3 reactions
BE 3 reactions

General note: Each primer sequence will be the end of the indicated gene to show us wether the joining/ligations worked correctly (VF is the promoter/gene/juction)
To do: Submit to MBSU

to the top

September 15

Schedule:

And yet another crazy weekend...

8-11 - ED,MC
General Note:We have cloned all 5 genes in series, in to differnt orders. Waiting for I0500 which couls be completed on monday. To make sure we have cloned correctly will also need to wait for the squencing results. This weekdn we will clone the 5 gense in 2 differnt orders. The digest have already been done
Gel extraction of gel bands of XBA,PST of BBDBBE and BEDBBB. THese can be used to cone into I0500 J61003
Ligations of DBBB into BE and DBBE into DBBEBB
Leave at 20 degrees celsius for 10 hours
5-8 - NK Cant find the competent cells.
Competent cells are in -80 freezer 2nd shelf from the bottom-ML, NG

to the top

September 16

Schedule: Continued...

8-11 ED, JG
Transform ligations of DBBEBB and DBBBBE into competent cells.
Plated on AMP with whole ligations
General Info: When DBBEBB and DBBBBE are complete run sequence reaction
Follow "flouresence sequence reaction" protocol

11-2 VH, CZ

2-5 MC, JP

5-8 - ML, NG
No growth on DBBBBE or DBBBBE at 1700
Retransformed into competent cells DBBEBB and DBBBBE
Plated 2 of each and lover overnight at 37 degrees

to the top

September 17

AM - JG (800 hrs - 930hrs),MC (@ 800hrs)
- delivered MSBU sequencing samples
- O/days of Ligations from yesterday

NB: AMP plates are marked with a red streak down the SIDE of the plate. if it does not have this - then it is NOT AMP

ML (~10:30-1:00)

To do:
miniprep of DBBEBB and DBBBBE & glycerol stocks
restrict with (1)XBA/PST, (2)SPE/PST
Ruun gel of UNCut DBBEBB and DBBBBE, Cut with XBA/PST and CUT with SPE/PST
GEl extract XBA/PST bands


to the top

September 18

NK - 8 AM
Sorry guys, I havent done mini-preps before so just incase I mess up i decided not do it. Instead I made a gel for tonight and update the wiki (even the missing parts from before).

VH - (@1pm)

AL - 12-2pm

Lab Notes:
Mini preped DBEBB and DBBBE, 4 overnights each. Made glycerol stocks of overnights (in -80 deg)

NK-6PM

Lab Notes:
Restrict DBEBB and DBBBE with XBA and PST, and SPE and PST.

to the top

September 19

if you're the first one in; I0500 arrived - pop by and give Mike a visit!:)

MC - in the AM - unsure what time because has to be downtown for a class project @900hrs (hoping to get out of there within a hour) so maybe 10/1030?

ML - ~10:30 - 1:00

AL - ~1:00 - 2:00

Last Wednesday there was a lab class in our lab from 2-5, is this going to be a regular occurence? -VH

YES - MC

VH, see notes on Sept 12. - AL

ED- 6PM

Lab Notes:

Picked up I0500 from Mike and plated on KAN plates.

Made a gel with EtBr in the gel.

Ran a gel of the digests that occurred on September 18th.

Took picture of gel for analysis tomorrow.

to the top

September 20

NK - 930 AM

VH - (@1PM)

JG, MC- (@5PM)

JP- late

Lab Notes:

Picked single colonies from growth on I0500 plates and made overnights and replated on kan plates.

Restrictions on DBBEBB and DBBBE are restarted, XPA and PST, SPE and PST.

Sequencing reactions of Buddy, Betty, Benny, Enny and DB.


to the top

September 21

AM - MC, JG (@ 800hrs),

ML (~10:30 - 1:00)

AL - ~12:30 - 2:00

CZ-2:15PM
ED - 4 PM

Lab Notes:

Restricted I0500 with ECO and XBA.

Ran a gel of digested I0500.

Took a picture of gel for analysis in the following lab day.

to the top

September 22

ED 9-12

NG 12-3

NK 230-530

JP evening

Lab Notes:

Digested J61003 with ECO and XBA.

Digested I0500 with ECO and SPE.

Made a gel and ran the restrictions described above.

Gel Extracted J61003 band from the gel. (Stored in -20 deg)

to the top

September 23

Poster Meeting @ 11:00am Meet in sub By the Subway--JG

ED 9-12

NG 12-3

NK 230-530

Lab Notes:

Repeat digestion of I0500 with 16 microlitres this time.

Ran on a gel, but did not provide a good picture and discarded.

to the top

September 24

AM -JG @ 8000hrs
MC @ 845 - going to stop by dean of students' to pick up swag first.


PM - NK @5
sorry, cant make it till 630

Lab Notes:

Started overdays of I0500 picked colonies. (Left in shaker at 37 deg)

Did a mini prep on I0500, followed protocols in Fermentas Kit

to the top

September 25

930-1230 NK

1-ish - AL

2pm-ish - VH

TO DO LIST:

1)

looking through the book to last thursday at my sequencing reactions and figure out exactly what samples I used for X-2, X-3, and X-4?

2)

If there is not much left (less than 20 microL), can you transform into bacteria so we can complete another mini? (only 1 transformation for each)

3)

place each of those tubes in a rack or something and leave directions so wayne can find it.

4)

X-1 has two prefixes, so its garbage, but X-5 might be ok. I couldn't find a terminator or a suffix. So... Can you complete a restriction on X-5 with Eco/Spe and Eco/Pst and run on a gel to make sure it cuts properly (and therefore those restriction sites exist)

5)

run sequencing reaction on more X-1 and X-5's (look at the chart erin made from back in the day - its a fold out piece of paper in the master book)

Lab Notes:

Digest I0500 with ECO and SPE - only half completed because ran out of SPE.



to the top

September 26

ML

Lab Notes:

Completed digests from yesterday that could not be finished due to a lack of SPE.

Ran a gel of products of digest but did not yield a good picture and gel was discarded.


to the top

September 27

NK 930-1230

VH - 2pm-ish

JP- evening

Lab Notes:

Redid overnights of I0500 so that they can be Re-minid.

Ran a new gel of the previous minid I0500s to see what is wrong with them. Result shows that there is not enough DNA for these samples to be usefull.

Started PCR for Thiolase.

Made overnights of Buddy in B0034 using the glycerol stocks.

to the top

September 28

JG & MC - 8:00AM

1-ish - AL

CZ 2:30pm
Redid miniprep of I0500 induced by IPTG(1C,1D,2C)and elute in 40 microlitre
Ran 3microliter ona gel but nothing appeared
Miniprep discarded because of lack of DNA
James took 1D culture ands ub culture and perhaps induce with IPTH again.
Restarted 1C and 2C (5ml LB, 5microlitre K, 100microlitre culture)

to the top

September 29

ED 9:00 am
Made of gel of James's Miniprep digests
Digest I0500 with ECORI and SPE
Transformations of Ligations Enny + J61003 and Betty + J61003

NK 1130-230
Loaded gel but samples were incorrectly loaded

CZ 2:00 pm
Loaded gel of Erin's digests
Gel extraction
Ligation with J61003 E, X

Note:The new TAE is taking much longer to solidify when 1%.

JP evening
Tholase PCR
Sequencing reactions of DB in Boo and Buddy in Boo


to the top

September 30

ED 9:00 Am
Transformed Buddy+J61003, I0500+J61003 #1 and #2
Plated all cells on AMP
O/Ns of Enny+J61003 and Benny+J61003
NG 12:00 am

JP
Tholase blunt end topo reaction
Completed reaction and tholase mix is in orange PCR tube rack at -20

Note:
1) We need XGAL!!
2) Colonies that are blue do not have thiolase in them, colonies that are wight do have thiolase in them.


to the top


UofA iGEM Home
To August 2007

Retrieved from "http://2007.igem.org/wiki/index.php/Alberta/Calender/September"