"

From 2010.igem.org

Revision as of 01:33, 27 October 2010 (view source) Mentler2 (Talk | contribs) (→Protocols) ← Older edit		Revision as of 01:33, 27 October 2010 (view source) Mentler2 (Talk | contribs) (→Protocols) Newer edit →
Line 9:		Line 9:
	# Estimate the intensities of your insert and vector where your insert (usually less intense) is considered 1 and your vector is x times as bright.		# Estimate the intensities of your insert and vector where your insert (usually less intense) is considered 1 and your vector is x times as bright.
	# Once intensity is determined perform the following equation:		# Once intensity is determined perform the following equation:
-	𝐿𝑖=3𝐿𝑣𝑆𝑖𝑆𝑣𝐼𝑣𝐼𝑖𝑉𝑖𝑉𝑣	+	𝐿𝑖=3𝐿𝑣𝑆𝑖𝑆𝑣𝐼𝑣𝐼𝑖𝑉𝑖𝑉𝑣<br>
		+
	L = Ligation volume S = Size of fragments I = Intensity of fragments		L = Ligation volume S = Size of fragments I = Intensity of fragments
	V = Volume ran down gel i = Insert v = Vector		V = Volume ran down gel i = Insert v = Vector
		+
	# Ligation volume (Lv) for the vector should be approximately 2 µl.		# Ligation volume (Lv) for the vector should be approximately 2 µl.
	# The ratio for the ligation in the previous equation is 3:1 insert:vector but can be done 6:1 by replacing the 3 with a 6.		# The ratio for the ligation in the previous equation is 3:1 insert:vector but can be done 6:1 by replacing the 3 with a 6.

---

Revision as of 01:33, 27 October 2010

Contents 1 Protocols 1.1 Ligations 1.2 Making Electrocompetent Cells 1.3 Site Directed Mutagenesis

Protocols

Ligations

Set-up:

1. Run a gel of your digestions and take a picture.
2. Estimate the intensities of your insert and vector where your insert (usually less intense) is considered 1 and your vector is x times as bright.
3. Once intensity is determined perform the following equation:

𝐿𝑖=3𝐿𝑣𝑆𝑖𝑆𝑣𝐼𝑣𝐼𝑖𝑉𝑖𝑉𝑣

L = Ligation volume S = Size of fragments I = Intensity of fragments V = Volume ran down gel i = Insert v = Vector

1. Ligation volume (Lv) for the vector should be approximately 2 µl.
2. The ratio for the ligation in the previous equation is 3:1 insert:vector but can be done 6:1 by replacing the 3 with a 6.

Reaction Mix:
• 2 µl – Vector
• Li µl – Insert
• 2 µl – 10x Buffer
• dH20 to 19 µl
• 1 µl – T4 DNA Ligase
TOTAL – 20 µl Procedure:

1. Add appropriate amounts of dH20, Vector, and Insert in a PCR tube (200 µl). Once added, heat mixture to 65o C for 5 min. This will remove all items that are already annealed to each other causing inefficient ligation.
2. Add then appropriate amounts of 10x Buffer and T4 DNA Ligase. Make sure not to pipette up and down or vortex to mix, this will shear the ligase. Gently swirl with the tip of your pipette to mix.
3. Incubate reaction at room temperature for 30 minutes.
4. After incubation heat inactivate the ligase by another incubation at 80o C for 20 min.

NOTE: The ligase buffer should smell like wet dog. If you smell nothing from the tube, then the buffer is old and useless.

Making Electrocompetent Cells

SOB
2% tryptone
0.5% yeast extract
10 mM NaCl
2.5 mM KCl
10 mM MgCl2
10 mM MgSO4

SOC
SOB + 20 mM glucose

Sterile 10% glycerol (can be autoclaved) is needed for the washes. The volume of 10% glycerol needed is 2X the culture volume (for example, a 500 ml culture requires 1L of 10% glycerol).

Procedure (for 2, 250 ml cultures)

1. Inoculate 1 colony from a fresh plate of the strain to be made electrocompetent into 10 ml of SOB in a 125 ml flask and incubate for 16-18 hours at 37oC and 250 rpm.
2. Have ready 2, 1 L flasks containing 250 ml each of SOB pre-warmed to 37°C. Add two drops of the overnight culture to each of the flasks.
3. Shake at 37°C and 250 rpm until the cultures reach an OD600 of 0.5-0.7. Be sure to turn on centrifuge and cool rotor to 4°C well in advance of harvesting cells. Be sure to place 1 L of 10% glycerol on ice well in advance of harvesting cells
4. Place cultures on ice for 15 minutes. From this point on the cultures must be kept ice cold. Pour each 250 ml culture into chilled 500 ml (or 1000 ml) centrifuge bottles.
5. Centrifuge at 5000 rpm for 10 min. Pour off the supernatant and aspirate any residual broth.
6. Add 250 ml of glycerol to each of the centrifuge bottles and completely suspend the cells by pipetting up and down.
7. Centrifuge at 5000 rpm for 10 min. Pour off the supernatant, it is not necessary to aspirate. Completely suspend the cells as before.
8. Pour off the supernatant and suspend the cells in the residual glycerol by pipetting up and down.
9. At this point you can electroporate or freeze the cells away. To freeze, Add 100 microliters of the culture to microcentrifuge tubes on ice. Once you have used all of the culture transfer the tubes to dry ice for 10 minutes. Once the cultures are frozen transfer them to a -80°C freezer. The cultures should be good for >6 months.

Site Directed Mutagenesis

Procedure modified from [http://www.genomics.agilent.com/files/Manual/200555B_01.pdf Stratagene QuikChange II Protocol]

Materials

• PFU Ultra Polymerase (high fidelity)
• 10X Reaction Buffer
• DpnI (20U/μL)
• dNTPs
• Competent Cells

General Overview
1. Design primers
2. Mutant strand synthesis (PCR)
3. DpnI digestion of template
4. Transform and plate
Primer Design Considerations
• Both primers must contain desired mutation and anneal to same sequence on opposite strands of the plasmid.
• Keep the Primers aruond 25-45 bp long with 10-15 bp on either side of the mutated base.
• Keep the melting temperature greater than or equal to 78°C
Tm=81.5+,41(%GC)-675/N-%mismatch where N is the length of the primer
• Try to keep the primers to a minimum GC content of 40% and end the primer in GC for a clamp.
• Make sure primers are in excess to template
PCR

Ingredient	Amount
10X Buffer	5 μL
Template	20 ng
Primer 1	125 ng
Primer 2	125 ng
10 mM dNTPs	1 μL
Polymerase	1 μL
H2O	Bring to 50 μL

Program:

95°C	3 min
95°C	30 sec
annealing temp	1 min
72°C	1 min/Kb
go to step 2	12X
72°C	1 min
hold at 4°C

PCR Purification via Promega Kit
DpnI Digestion

DNA	500 ng
Buffer 4	5 μL
BSA	.5 μL
DpnI	1 μL
H2O	Bring to 50 μL

Incubate at 37°C for 1 hour, inactivate at 80°C for 20 min.
Transform via electroporation