Lab Knowledge Base

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===Wiki===
===Wiki===
*Welcome to the Lab Wiki for Mark Farmer's Lab.  This is the place to find procedures, news, and answers to commonly asked questions.
*Welcome to the Lab Wiki for Mark Farmer's Lab.  This is the place to find procedures, news, and answers to commonly asked questions.
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*If you are new to this wiki, you will need an account in order to edit pages.  Talk to [[Sarah]] about getting an account set up if you would like to contribute.
+
*If you are new to this wiki, you will need an account in order to edit pages.  Talk to [[Katy]] about getting an account set up if you would like to contribute.
*You can upload pictures, word, excel, and pdf documents.
*You can upload pictures, word, excel, and pdf documents.
*If you are new to wiki editing, check out the wiki help for how to edit articles in a wiki, then use the existing pages as templates and examples of how to create links, upload files, and display images.
*If you are new to wiki editing, check out the wiki help for how to edit articles in a wiki, then use the existing pages as templates and examples of how to create links, upload files, and display images.
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===Cultures & Lab Announcements===
===Cultures & Lab Announcements===
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*Friday the 22nd is '''Brandon's 19th Birthday''' and we will have cake during lab meeting (Wednesday the 27th, ''Thanks for volunteering to make the cake, Caitlin!'')
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Next lab assistants meeting
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'''TBA'''
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*'''The Association of Women in Sciences (AWIS)'''
*'''The Association of Women in Sciences (AWIS)'''
 +
== Things To Do ==
 +
=== Priority ===
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== Pressing Things TO DO! ==  
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=== Next Lab Meeting January 14 2pm ===
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=== Next Lab Meeting (26March08) ===
 
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#Check to see if we are low on small and large plug seal flasks.
 
 +
=== January ===
 +
*If you have any questions call/email Katy
 +
*Empty all tip/trash box(s)/containers on gel and molecular benches every Wed & Fri
 +
*Wipe down all molecular work benches with the [[FIX]] 70% Ethanol squirt bottle every Wed & Fri
 +
*Check water bath on molecular work bench if low on water please add DI H2O check every Wed & Fri
 +
*If you're not sure what to do see '''Are you a Lab Assistant with free time on your hands?'''
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=== Today (26Mar08) ===
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=== List of Organisms needed by MSU ===
 +
Please find these organisms and make an additional tube of them.  If any are not alive or contaminated please indicate below next to the three letter codes, please email Katy with any questions
 +
*CCM '''xx, ok'''
 +
*EDS '''not moving'''
 +
*EPE
 +
*ETM
 +
*ELU '''NOTHING IN HERE'''
 +
*HYO
 +
*KHQ
 +
*LXC '''x NOT MOVING'''
 +
*PET
 +
*SXD '''xx, ok, some dead'''
 +
*SXE  '''xx, ok, but some dead'''
 +
*SUL '''xx, good'''
 +
*TRT
 +
*TUB '''xx, good, but may be CONTAMINATED'''
 +
*TUV '''xxx, very good'''
 +
*TUY '''xxx, very good'''
 +
*TUX '''xx, good'''
 +
*TUM '''xx, good'''
 +
*TUP '''xxx, very good'''
 +
*TUO '''xxxx, very good'''
 +
*LXB '''xxx, good'''
 +
*LXF '''x CONTAMINATED'''
 +
*LXH '''xx, ok'''
 +
*LXJ '''xx, ok'''
 +
*LXR '''xxx, very good contam?'''
 +
*LXT '''xx, good'''
 +
*LYE '''xxx, good'''
 +
*LYF
 +
*LYI '''xx good but contaminated'''
 +
*LUF '''xxx, very good'''
 +
*LUK '''xx, good'''
 +
*LUT '''xxx, very good'''
 +
*LUY '''xxx, very good'''
 +
*TSP '''xxxx, very good'''
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*Organisms with no info were not found/ are not in MSU test tube rack.
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'''Things that must be done today:'''
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If not finished, the last person to leave should e-mail SEJ or CC what's left to be done (depending on who it's for).
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*Make more [[PE]] media.
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*Spin down RMN (6,2 large flasks). Be sure to use a sterile scraper to scrape cells off the bottom. Replacement media is in incubator 5 on the middle shelf.
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'''Priority:'''
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*Need more [[CH]] Media(on the last bottle).
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*Refill agarose tubes with GenePure LE Quick Dissolve Agarose (use small bottle first...in drawer with measuring supplies for your ease...please make a couple more ~0.6g tubes)
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*Please check small flasks on 2D '''JI checked first 2 rows on right b/c they were priority- see notebook 19mar08'''
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*SEJ's - Please do DNA extractions on the following organisms (be sure to check if they original spin down was done on Log phase cells before you combine/extract them):
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**Cell Box 2: SBR, STB, TZR, THA, TPL, TUM, TVI'''SBR done BP'''
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**Cell Box 3: LXS, SNB, LUO, SXA, SSA, MUC=MUR, SSC
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**Cell Box 4: ELU, SMA, SUZ, SEU, TUA
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**Cell Box 6: TBR, LUE, TVS, TRG, TUJ, SMC
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**Cell Box 7: SUN, CNT, TUX, TUK, SUY, SBA,
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**Cell Box 8: SXB, SUI
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**Cell Box 9: TOG, TUV, TEP, TSP, SCP
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**Cell Box 10: TLF=TLV (some tubes are mislabeled as TLF when they should be TLV=''Trachelomonas lefevrei'')
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*do spin downs of big flasks this week if they are ready...'''JI did flasks on 4B and ELU by window...still need to do flasks on 4A and ETM in incubator #1!!!'''
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*switch any of SEJ's big flasks that are in the plug-sealed big flasks into the vented big flasks if they are still healthy and if they are not healthy or are dead/contaminated, then start new big flask from uncontaminated tube'''(Done ST, 29feb08)'''
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*Empty all tip/trash box(s)/containers on gel and molecular benches every '''Wed''' & Fri
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*Wipe down all molecular work benches with the [[FIX]] 70% Ethanol squirt bottle every '''Wed''' & Fri
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'''Cultures:'''
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*When checking cultures, please put aside any cultures with fungus for BP fungal treatments. Let him know where they've been put.
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*Brandon will be doing fungal treatment experiments using Sharan's notes in Lab Binder
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**Need to make 2 small flasks (one labeled microscopy) of the following (indicates test tube location):
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***LUV (4C-backup)'''test tube contaminated with rodifers; used older test tube to make small flask; need to watch for contamination'''
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***TCI (4g)'''done CS'''
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***LXF (1g)'''done CS'''
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***LXI (4c-backup)'''done BP'''
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***LXJ (9h)'''test tubes contaminated with ciliates'''
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***LXH (1f)'''done CS'''
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***TUB '''test tubes contaminated'''
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***TUO JI did small flask (currently in 4), but seems like two different sizes of Trachs, redo small flask from uncontaminated tube or single cell isolate to get both types of cells isolated and grown up in small flasks '''done CS'''
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***SNB '''done CS'''
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***THB '''done CS'''
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***LUT (13d) '''done CS'''
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***TUN (?) '''can't find'''
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***TUK '''done CS'''
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***LUF (8f) '''done CS'''
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***LXR (6c) '''done CS'''
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***TUX '''done CS'''
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***LXT '''done CS'''
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***LYI (2d) '''done CS'''
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***LUK (9a) '''done CS'''
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***LYE (7f) '''done CS'''
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**Need to make 1 small flask for DNA (indicated test tube location):
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***LYA (7C)'''Contaminated with cilliates + rodifers; made a small flask - need to watch for contamination'''
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***SXD (4i) '''Dead in notebook 30Jan08'''
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***LXL (1d) '''done CS'''
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***SXE (5f)'''done BP'''
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***TSP (10b)'''done BP'''
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***TUY (3b)'''done BP'''
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***TXB (4d) '''done CS'''
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***TXG (1c) done CS...please do again b/c no trach cells on 26Feb08, only ciliates in small flask '''test tubes contain no living cells or ciliates; may have 1 cell in test tube 4 Oct 07 - did not make small flask'''
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***LXW (6f) '''done CS'''
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***LXX (1i) '''done CS'''
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***LYB (?) '''Can't find'''
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***LUW (9b) '''done CS'''
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***LUO (4c-backup) '''can't find CS''';'''This was thrown out 30Jan08, but we still have a good big flask for it- JI'''
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***LYS (13j '''done CS'''
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***LYT (13i) '''done CS'''
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***LUA (13h) '''done CS'''
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***LUC (13g) '''done CS'''
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***LUD (13f) '''done CS'''
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***LUG (13e) '''done CS'''
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***LYP (?) '''Can't find'''
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***LYD (7e) '''done CS'''
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***LYG (7h) '''done CS'''
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***LXN (?) '''Can't Find'''
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***SUM (?) '''Can't Find'''
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***TVL '''test tubes contaminated'''
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***LYU '''test tubes contaminated'''
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***LXW '''done CS'''
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***LUW '''done CS'''
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***LXZ '''done CS'''
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***LXP '''done CS'''
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***LUU '''done CS'''
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***SUL '''done CS'''
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'''Lab Assistants, Please Update Sarah/Christina On:'''
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*'''Updates for Sarah'''
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**list of all cultures I need in small flasks that have been started (any moved to big flasks yet?)
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**list of all cultures I need in small flasks that are contaminated (and preferably what they are contaminated with)
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*'''Updates for Christina'''
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*'''Updates for Katy'''
 +
**katy, i have posted the info on how to prep and ship the cultures to MSU on this page [[Shipping Cultures Tubes to MSU]]...let me know if you have any questions '''SEJ 08Oct09'''
[[Notes for Sarah]]
[[Notes for Sarah]]
 +
*Euglenozoa AToL
== Are you a Lab Assistant with free time on your hands? ==
== Are you a Lab Assistant with free time on your hands? ==
 +
*keep up with washing, drying and autoclaving the glass volumetric pipets so we don't run out (5, 10, 25mL)
 +
*put cotton in the tops of pasteur pipets and fill the containers (by the dishwashing station) and autoclave them
*Make any media that needs to be made (generally [[AF-6 Medium]], [[ESNW]] or [[Hay Infusion]])
*Make any media that needs to be made (generally [[AF-6 Medium]], [[ESNW]] or [[Hay Infusion]])
*[[Autoclave]] media using the liquid cycle (be sure you label with autoclave tape)
*[[Autoclave]] media using the liquid cycle (be sure you label with autoclave tape)
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== Lab Binder & Notebook ==
== Lab Binder & Notebook ==
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*[[Protocols]]
 
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*Media and Molecular [[Recipes]]
 
*[[Culture Inventory]]
*[[Culture Inventory]]
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*[[Inventory]]
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*[[Culture Ordering Information]]
*[[Instructional Information]]
*[[Instructional Information]]
 +
*[[Lab Supplies]]
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*Media and Molecular [[Recipes]]
 +
*[[Protocols]]
*[[Recipes not Currently Used]]
*[[Recipes not Currently Used]]
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*[[Culture Ordering Information]]
 
== Phylogenetics and Systematics of Euglenozoa ==
== Phylogenetics and Systematics of Euglenozoa ==

Current revision as of 18:57, 14 January 2010

Contents

News

Wiki

  • Welcome to the Lab Wiki for Mark Farmer's Lab. This is the place to find procedures, news, and answers to commonly asked questions.
  • If you are new to this wiki, you will need an account in order to edit pages. Talk to Katy about getting an account set up if you would like to contribute.
  • You can upload pictures, word, excel, and pdf documents.
  • If you are new to wiki editing, check out the wiki help for how to edit articles in a wiki, then use the existing pages as templates and examples of how to create links, upload files, and display images.


Cultures & Lab Announcements

Next lab assistants meeting TBA


Professional Enrichment

  • The Association of Women in Sciences (AWIS)

Things To Do

Priority

Next Lab Meeting January 14 2pm

January

  • If you have any questions call/email Katy
  • Empty all tip/trash box(s)/containers on gel and molecular benches every Wed & Fri
  • Wipe down all molecular work benches with the FIX 70% Ethanol squirt bottle every Wed & Fri
  • Check water bath on molecular work bench if low on water please add DI H2O check every Wed & Fri
  • If you're not sure what to do see Are you a Lab Assistant with free time on your hands?

List of Organisms needed by MSU

Please find these organisms and make an additional tube of them. If any are not alive or contaminated please indicate below next to the three letter codes, please email Katy with any questions

  • CCM xx, ok
  • EDS not moving
  • EPE
  • ETM
  • ELU NOTHING IN HERE
  • HYO
  • KHQ
  • LXC x NOT MOVING
  • PET
  • SXD xx, ok, some dead
  • SXE xx, ok, but some dead
  • SUL xx, good
  • TRT
  • TUB xx, good, but may be CONTAMINATED
  • TUV xxx, very good
  • TUY xxx, very good
  • TUX xx, good
  • TUM xx, good
  • TUP xxx, very good
  • TUO xxxx, very good
  • LXB xxx, good
  • LXF x CONTAMINATED
  • LXH xx, ok
  • LXJ xx, ok
  • LXR xxx, very good contam?
  • LXT xx, good
  • LYE xxx, good
  • LYF
  • LYI xx good but contaminated
  • LUF xxx, very good
  • LUK xx, good
  • LUT xxx, very good
  • LUY xxx, very good
  • TSP xxxx, very good
  • Organisms with no info were not found/ are not in MSU test tube rack.


  • Updates for Katy
    • katy, i have posted the info on how to prep and ship the cultures to MSU on this page Shipping Cultures Tubes to MSU...let me know if you have any questions SEJ 08Oct09

Notes for Sarah

  • Euglenozoa AToL

Are you a Lab Assistant with free time on your hands?

  • keep up with washing, drying and autoclaving the glass volumetric pipets so we don't run out (5, 10, 25mL)
  • put cotton in the tops of pasteur pipets and fill the containers (by the dishwashing station) and autoclave them
  • Make any media that needs to be made (generally AF-6 Medium, ESNW or Hay Infusion)
  • Autoclave media using the liquid cycle (be sure you label with autoclave tape)
  • Using sterile technique, add any additional ingredients to complete media post-autoclaving (eg. vitamins)
  • Wash test tubes, media containers and their respective caps (keep LIVE and FIX glassware separated)
  • Autoclave the test tubes, media containers, 9" pasteur pipets, pipet tip box(es), volumetric pipets, etc. in appropriate containers with containers underneath if available
  • Using sterile techniqe, add media to the autoclaved tubes or sterile culture flasks
  • Check and make notes of cultures without opening the tubes or culture flasks using the appropriate microscopes. Some cultures need to be checked daily, weekly, bi-weekly or monthly depending on their growth patterns.
  • Make transfers of healthy cultures (all culture information can be found on the Cumulative Culture Inventory.xls sheet on the Farmer Lab PC desktop)
    • tubes
    • big/small flasks
  • Spin down log phase cells in big culture flasks and rejuvenate with fresh media (aseptically)
  • Extract DNA from concentrated cells and update the DNA.xls sheet
  • Qualify/Quantify DNA on Nanodrop
  • Maintain molecular buffers, reagents
  • Maintain at least one carboy of DI water
  • Keep everything clean and organized
  • Ask if anyone in the lab needs anything done



Lab Binder & Notebook

Phylogenetics and Systematics of Euglenozoa

Documents



See Also

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