Difference between revisions of "Reagent Recipes"

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# Put catalase into a 15ml or 50ml plastic tube.
 
# Put catalase into a 15ml or 50ml plastic tube.
 
# Pipet in PBS, measuring out the volume using a serological pipet.
 
# Pipet in PBS, measuring out the volume using a serological pipet.
# Gently shake until dissolved.
+
# Gently shake until dissolved. DO NOT VORTEX.
 
# Sterilely filter solution using a syringe filter and place into a fresh, sterile plastic tube.
 
# Sterilely filter solution using a syringe filter and place into a fresh, sterile plastic tube.
# Label top with contents and date; cover with foil to prevent exposure to light.
+
# Aliquot 1 ml in 1.5 ml microcenterfuge tubes.
 +
# Label top with contents and date; limit exposure to light.
 
# Keep in refrigerator
 
# Keep in refrigerator

Revision as of 14:38, 10 July 2019

Reagent Information

Reagent Abbreviation Stock Solution

Concentration

Solvent Stock Concentration to

Working Concentration

Notes
Bromo-chloro-indolyl-galactopyranoside X-gal 20mg/ml Dimethylformamide (DMF) 250x Use DMF in a chemical hood
Isopropyl β-D-1-thiogalactopyranoside IPTG 0.1M H2O 1000x Light sensitive. Molecular weight: 238.31 g/mol

Glycerol for freezing aliquots

We use sterile 80% glycerol in water. We dilute this 1:3 (400ul 80% glycerol; 1200ul culture) for creating freezer stocks with a final glycerol concentration of 20%.

10x PBS

Used to create 1x PBS for dilution or washing cells of any species.

For 1 liter:

  • NaCl 80g
  • KCl 2g
  • Na2HPO4 14.4g
  • KH2PO4 2.4g

Stir salts with MilliQ water. This may take a significant time to dissolve!

Adjust pH with NaOH to 7.4. This will take a significant amount of NaOH; add in 200ul increments.


Tris Buffer

For Tris buffer at pH 8.0 (at 25 degrees)

  • 4.44 g/L Tris HCl
  • 2.65 g/L Tris Base

Do not adjust pH or check the pH with the MEE lab pH probe. This will destroy the probe!

Catalase

  1. Calculate the amount of catalase needed; final concentration should be 30,000U / ml. Each batch may require a different number of milligrams of catalase.
  2. Use the precise balance of Karl's lab to measure out the catalase. Use a folded piece of weighing paper instead of a weighboat.
  3. Put catalase into a 15ml or 50ml plastic tube.
  4. Pipet in PBS, measuring out the volume using a serological pipet.
  5. Gently shake until dissolved. DO NOT VORTEX.
  6. Sterilely filter solution using a syringe filter and place into a fresh, sterile plastic tube.
  7. Aliquot 1 ml in 1.5 ml microcenterfuge tubes.
  8. Label top with contents and date; limit exposure to light.
  9. Keep in refrigerator