Difference between revisions of "PhiX:Recipes"

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'''SB Buffer for high-speed, low-temp agarose electrophoresis'''<br>
+
'''HIGH-SPEED GEL ELECTROPHORESIS'''<br>
 +
'''SB Buffer'''<br>
 
45g boric acid<br>
 
45g boric acid<br>
8g sodium hydroxide pellets
+
8g sodium hydroxide pellets<br>
 
water to 1 litre
 
water to 1 litre
  
'''BE Buffer (one litre; 50mM Na<sub>2</sub>B<sub>4</sub>O<sub>7</sub>; 5.0mM EDTA)'''<br>
+
 
 +
'''PHAGE ELUTION'''<br>
 +
'''BE Buffer (50mM Na<sub>2</sub>B<sub>4</sub>O<sub>7</sub>; 5.0mM EDTA)'''<br>
 
19.1g Na<sub>2</sub>B<sub>4</sub>O<sub>7</sub>.10H<sub>2</sub>O<br>
 
19.1g Na<sub>2</sub>B<sub>4</sub>O<sub>7</sub>.10H<sub>2</sub>O<br>
 
1.86g EDTA (disodium salt)<br>
 
1.86g EDTA (disodium salt)<br>
 
water to 1 litre
 
water to 1 litre
  
 +
 +
'''PHAGE GROWTH'''<br>
 +
'''LB Buffer'''<br>
 +
10g tryptone<br>
 +
5g yeast extract<br>
 +
10g NaCl<br>
 +
water to 1 litre, mix and autoclave<br>
 +
after autoclaving add CaCl<sub>2</sub> to 2mM (2ml 1M per litre) and MgCl<sub>2</sub> to 10mM (10ml 1M per litre)
 +
 +
''For plate agar:''
 +
add 15g Bacto brand agar per litre;
 +
no need to add salts
 +
 +
''For top agar:''
 +
add 7g Bacto brand agar per litre;
 +
after autoclaving add CaCl<sub>2</sub> (to 2mM) and MgCl<sub>2</sub> (to 10mM)
 +
 +
''Note:''
 +
Bentley Fane add CaCl<sub>2</sub> to 5mM
 +
 +
 +
'''PHAGE STORAGE/DILUTION'''<br>
 +
'''HFB Buffer (60mM NH<sub>4</sub>Cl; 90mM NaCl; 0.1M KCl; 0.1M Tris-HCl (pH 7.4); 1.0mM MgSO<sub>4</sub>; 1.0mM CaCl<sub>2</sub>)'''<br>
 +
''For 500ml 10× stock:''<br>
 +
125ml of 2.0 M Tris-HCl (pH 7.3) -- surely 250ml?<br>
 +
15g NH<sub>4</sub>Cl<br>
 +
2.5g NaCl<br>
 +
25g KCl<br>
 +
5.0ml 1.0 M MgSO<sub>4</sub><br>
 +
5.0ml 1.0M CaCl<sub>2</sub><br>
 +
water up to 500ml<br>
 +
 +
''For working solution:''
 +
dilute to 1× in water and autoclave
 +
 +
 +
'''NUCLEIC ACID SEPARATION'''<br>
 
'''Tris-saturated Phenol with antioxidant (with 100ml phenol)'''<br>
 
'''Tris-saturated Phenol with antioxidant (with 100ml phenol)'''<br>
 
add 100mg 8-hydroxyquinoline (i.e., 0.1% w/v)<br>
 
add 100mg 8-hydroxyquinoline (i.e., 0.1% w/v)<br>
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add 130ul 2-mercaptoethanol (0.2% of buffer phase)
 
add 130ul 2-mercaptoethanol (0.2% of buffer phase)
  
 +
 +
'''COMPONENT SOLUTIONS'''<br>
 
'''EDTA stock (0.5M)'''<br>
 
'''EDTA stock (0.5M)'''<br>
 
use disodium salt and pH to 8 with NaOH
 
use disodium salt and pH to 8 with NaOH

Latest revision as of 04:14, 7 August 2013

HIGH-SPEED GEL ELECTROPHORESIS
SB Buffer
45g boric acid
8g sodium hydroxide pellets
water to 1 litre


PHAGE ELUTION
BE Buffer (50mM Na2B4O7; 5.0mM EDTA)
19.1g Na2B4O7.10H2O
1.86g EDTA (disodium salt)
water to 1 litre


PHAGE GROWTH
LB Buffer
10g tryptone
5g yeast extract
10g NaCl
water to 1 litre, mix and autoclave
after autoclaving add CaCl2 to 2mM (2ml 1M per litre) and MgCl2 to 10mM (10ml 1M per litre)

For plate agar: add 15g Bacto brand agar per litre; no need to add salts

For top agar: add 7g Bacto brand agar per litre; after autoclaving add CaCl2 (to 2mM) and MgCl2 (to 10mM)

Note: Bentley Fane add CaCl2 to 5mM


PHAGE STORAGE/DILUTION
HFB Buffer (60mM NH4Cl; 90mM NaCl; 0.1M KCl; 0.1M Tris-HCl (pH 7.4); 1.0mM MgSO4; 1.0mM CaCl2)
For 500ml 10× stock:
125ml of 2.0 M Tris-HCl (pH 7.3) -- surely 250ml?
15g NH4Cl
2.5g NaCl
25g KCl
5.0ml 1.0 M MgSO4
5.0ml 1.0M CaCl2
water up to 500ml

For working solution: dilute to 1× in water and autoclave


NUCLEIC ACID SEPARATION
Tris-saturated Phenol with antioxidant (with 100ml phenol)
add 100mg 8-hydroxyquinoline (i.e., 0.1% w/v)
add equilibration buffer (-> pH 7.9) - 6.5ml of this in Sigma kit
add 130ul 2-mercaptoethanol (0.2% of buffer phase)


COMPONENT SOLUTIONS
EDTA stock (0.5M)
use disodium salt and pH to 8 with NaOH

SDS 20%
pre-bought - avoids fine powder

Tris-HCl stock (1M)
pH to 8 with HCl

Pronase to 20mg/ml
dissolve in nuclease-free water and store at -20oC

10 X PE1
200mM Tris pH 7.5
100mM MgCl2
200 mM NaCl
10 mM DTT

10 X PE2
200 mM Tris pH 7.5
100 mM MgCl2
100 mM DTT