APPENDIX I
		List of Reagents, in alphabetical
order 
		(* reagents used in Mol. Bio. Lab)
*Reagent - Storage Condition
*2X YT - store at room temp.
  - 900 ml water
  
- 16 g Bacto tryptone
  
- 10 g Bacto yeast extract
  
- 5 g NaCl
  
- Shake until dissolved and pH with 200 µl
  5 M NaOH
  
- adjust volume to 1 L
  
- autoclave
*agar plates
- store at room temp.
  - to 1 L of any medium, add 15 g of Bacto Agar
  
  
- autoclave to sterilize, pour while hot, rinse
  flask well before it hardens
*ammonium acetate, 7.5 M - store at room temp.
  - 50 ml water
  
- 57.75 g ammonium acetate
  
- adjust volume to 100 ml with H2O
*ampicillin (Fisher
#BP1760-25) - store at -20° C
  - 100 mg/ ml water - this is a 1000X stock solution
  
- filter sterilize with a 0.22 µm filter
  into a sterile container
*Blotto- store at 4° C
  - 7 g Dry Milk
- 10 mL 10X Tris Saline Stock
- 100 µL Tween 20
- 100µL Antifoam A
- Water to 100 mL
*CaCl2 solution - store at 
  +4° C
  - 60 mM CaCl2 
  
- 15% Glycerol
  
- 10 mM PIPES, pH 7
  
- Autoclave.
*chloroform, 100% - store at RT°
  - already prepared
 WARNING THIS IS A KNOWN MUTAGEN WEAR GLOVES
*competent bacteria (capable of taking up DNA)
- store at -70° C
  - already prepared (CaCl2 method)
*denaturing solution (for DNA) - store at RT°
*DNA loading dye - store at +4° C
  - for 10 ml of a 10X stock solution:
  
- 30% glycerol (v/v)
  
- a pinch of bromophenol blue
  
- a pinch of xylene cyanol FF
*DNAse, 10 mg/ ml - store at -20° C
  - CAUTION - THIS WILL DEGRADE ALL DNA SAMPLES SO
  BE CAREFUL 
  
- dilute the bottle of DNAse with sterile water
  so that the final concentration is 10 mg/ml (e.g. 10 mg plus 1 ml of water).
  
  
- Once it is dissolved, aliquot into 100 µl
  volumes and store at -20° C
*ECL Primary Wash- store at RT°
  - 0.4 % SDS (start with 20% SDS stock solution)
- 0.5X SSC
*ECL Secondary Wash- store at RT°
*EDTA, 0.5 M pH 8.0 - store at RT°
  - 93.0 g EDTA
  
- 350 ml of water and stir on magnetic stirring
  plate
  
- about 10 g NaOH pellets
  
- add 5 M NaOH until all EDTA is dissolved (this
  happens at pH 8.0)
  
- adjust volume up to 500 ml with water 
*ethidium bromide - store at +4° C
WARNING THIS IS A KNOWN MUTAGEN WEAR GLOVES
  - already prepared
  
- 10 mg/ ml in H20
*EtOH (ethanol) - store at RT° or +4° C
  - unless stated otherwise, it is 100% and from
  a "DNA only" bottle
*EtOH 70%, - store at RT°
or +4° C
*gelatin, 2% - store at RT°
  - 2g gelatin
  
- 100 ml water
  
- autoclave
*glacial acetic acid - store at RT°
*glucose, 10% - store at RT°
  - 70 ml water
  
- 10 g glucose
  
- water to 100 ml
  
- sterilize by filtration 
*glycerol, sterile RT°
*IPTG (isopropylthio- b - D -galactoside) -
store at -20° C
  - 8 ml water 
  
- 2 g IPTG
  
- adjust volume to 10 ml
  
- sterilize by filtration, aliquot in 1 ml volumes
  and store at -20° C
*LB - store at RT°
  - for 1 L of LB medium:
  
- 700 ml water
  
- 10 g Bacto Tryptone
  
- 5 g Yeast Extract
  
- 10 g NaCl (5 g for low salt version)
  
- 200 µl 5 M NaOH
  
- water up to 1L
  
- Autoclave in 2 X 1 L bottles, 500 ml in each
  bottle
*magnesium sulfate, 1 M - store at RT°
  - you should figure this one out
  
- MgSO4*7H20
  FW = 246.48
  
- make 100 ml total volume
  
- autoclave
*maltose, 20% (w/v) - store at RT°
  - 20 g maltose
  
- water up to 100 ml
  
- Sterilize by filtering through a 0.22 µm
  filter into a sterile bottle
*miniprep solution I - store at RT°
  - 15 ml of water
  
- 0.23 g glucose
  
- 0.626 ml 1 M Tris, pH 8.0
  
- 0.5 ml 0.5 M EDTA
  
- water up to 25 ml
*miniprep solution II - store at RT°
  - 0.4 ml 5 M NaOH
  
- 9.1 ml water
  
- 0.5 ml 20% SDS
*miniprep solution III - store at +4° C
  - 60 ml 5 M potassium acetate stock solution
  
- 11.5 ml glacial acetic acid
  
- 28.5 ml water
*neutralizing solution (for DNA) - store at
RT°
  - 1.5 M NaCl 
  
- 0.5 M Tris, pH 7.5
*Ponsceau S- store at RT°
  - 0.1% w/v Ponsceau S
- in 1% v/v acetic acid
*phenol/chloroform/isoamyl alcohol (Ameresco) - store 
  at +4° C
  - already prepared
  
- chloroform:isoamyl alcohol 24:1
  
- the above:phenol 1:1
  
- the phenol/chloroform is the bottom phase and
  the buffer is on top
 WARNING THIS IS A KNOWN MUTAGEN WEAR GLOVES
*phenol, saturated and buffered (pH 8.0) (Ameresco)
- store at +4° C
  - already prepared but the phenol is the bottom
  phase and the buffer is on top
 WARNING THIS IS A KNOWN MUTAGEN WEAR GLOVES
*potassium acetate, 5 M stock - store at RT°
  - 49.07 g potassium acetate
  
- water up to 100 ml
*proteinase K, 10 mg/ ml - store at -20° C
  - CAUTION - THIS WILL DEGRADE ALL PROTEIN SAMPLES
  SO BE CAREFUL
  
- dilute the bottle of proteinase K with sterile
  water
  
- so that the final concentration is 10 mg/ml (e.g.
  10 mg plus 1 ml of water). 
  
- Once it is dissolved, aliquot into 100 µl
  volumes and store at -20 
*RNAse, 10 mg/ ml (SIGMA# R-5125) - store at
-20° C
  - CAUTION - THIS WILL DEGRADE ALL RNA SAMPLES SO
  BE CAREFUL
  
- dilute the bottle of RNAse with sterile water
  so that the final 
  
- concentration is 10 mg/ml (e.g. 10 mg plus 1
  ml of water). Once it is dissolved, 
  
- aliquot into 100 µl volumes and store at
  -20° C
*sarkosyl (Sigma # L-5125) - store at RT°
  - 20% w/v YOU FIGURE OUT AMOUNTS
  
- mix powder and water and stir for a long time
  at RT°
*SDS (Sigma # L-5750) sodium dodecyl sulfate,
also called lauryl sulfate - store RT°
  - 20% w/v YOU FIGURE OUT AMOUNTS
  
- mix powder and water and stir for a long time
  at RT°
 WARNING: DO NOT BREATHE ANY SDS DUST - IT WILL MAKE
  YOU COUGH A LOT
*SM - store at RT°
  - for 1 L of SM:
  
- 5.8 g NaCl
  
- 2.0 g MgSO4
  .7H 2
  O
  
- 50 ml 1 M Tris, pH 7.5
  
- 5 ml 2% gelatin
  
- water up to 1 L
  
- Sterilize by autoclaving in 2 X 500 ml bottles
*sodium acetate, 3M - store at RT°
  - 40.8 g sodium acetate.3H20
  
- 50 ml water 
  
- pH 5.2 use glacial acetic acid
  
- pH 7.0 use dilute acetic acid
*sodium chloride, 5 M - store at RT°
  - you figure this one out
  
- FW = 58.44
  
- make 500 ml of this in water
*sodium hydroxide (CAUTION
- VERY CAUSTIC) - store at RT°
  - you figure this one out
  
- FW = 40.0
  
- make 100 ml of this in water
*SSC, 20X stock - store at RT°
  - 800 ml water 
  
- 175 g NaCl
  
- 88 g sodium citrate
  
- adjust pH to 7.0 with conc. HCl 
  
- adjust volume to 1 L
  
- autoclave
*TBE - Tris, Boric acid, EDTA - store at RT°
  - for 1L of a "5X" stock:
  
- 54 g Tris base
  
- 27.5 g boric acid
  
- 20 ml 0.5 M EDTA
  
- H 2 O up to 1 L
*TE - Tris, pH 8.0, EDTA - store at RT°
  - to make 50 ml of a 10X stock solution:
  
- 5 ml of 1 M Tris, pH 8.0
  
- 1 ml of 0.5 M EDTA
  
- 44 ml of H20
*TEN - store at +4°
C
  - 150 mM NaCl
  
- 10 mM EDTA
  
- 10 mM Tris-HCl, pH 8.0
  
*Tetracycline - store at -20° C
  - 5 mg/mL 100 ethanol (this is sterile due to ethanol)  
  
- final concentration = 50 µg/mL for high copy plasmids (e.g. pSB1A3);  stock is 100X
  
-  10 µg/mL for low or medium copy plasmids; stock is 500X
*top agarose or agar - store at RT°
  - 0.7 g agarose
  
- 100 ml H20
  
- autoclave in 2 X 100 ml bottles
*10X Transfer buffer stock (western blots)- store 
  at RT°
  - 30.3 g Tris Base
- 144.1 g glycine
- water to 1 L
*1X Transfer buffer (western blots)- store at 4° 
  C 
  - 100 mL 10X stock
- 500 mL water
- 200 mL methanol
- water to 1 L
- chill to 4° C
*Tris, 1 M - store at RT°
  - 121 g Tris base 
  
- 800 ml H20 
  
- pH with HCl  
    
      - pH 7.5 takes ~ 60 ml HCl 
- pH 8.0 takes ~ 40 ml HCl
 
- use pH meter to home in on correct pH 
  
- H20 up to 1 L 
  
- autoclave 
*10X Tris Saline- store at RT°
  - 6.05 g Tris Base
- 43.9 g NaCl
- water to 500 mL
*Turbo Denaturing Buffer- store at RT°
  - 3 M NaCl
- 0.4 M NaOH
- water to 1 L
*Turbo Transfer Buffer- store at RT°
  - 3M NaCl
- 8 mM NaOH
- 2 mM Sarkosyl
*5X Turbo Neutralizing Buffer- store at RT°
  - 1 M phosphate buffer, pH 6.8
- 79.5 g Na2HPO4
- 52.39 g anhydrous NaH2PO4 or 60.25 g NaH2PO4.H2O
*X-gal (5-bromo-4-chloro-3-indoyl- b - D -galactoside) 
  - store at -20° C
  - 20 mg/ml in dimethylformamide in a glass container
  
- wrap in foil
  
- store at -20° C
Lab Schedule Outlined
Lab Schedule In Context of Research Project
		
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