Team:Amsterdam/Notebook/Protocols/Digestion
From 2011.igem.org
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- | =Digestion= | + | =Digestion: Making new constructs= |
We used this protocol for the digestion of the biobricks. | We used this protocol for the digestion of the biobricks. | ||
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2. Incubate at 80C for 20min to heat kill the enzymes.<br> | 2. Incubate at 80C for 20min to heat kill the enzymes.<br> | ||
3. Store at -4C. | 3. Store at -4C. | ||
- | |||
- | |||
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8. fill each of the three samples up to 10 ul including LD and check them on agarose gel.<br> | 8. fill each of the three samples up to 10 ul including LD and check them on agarose gel.<br> | ||
+ | =Digestion: Changing the backbone= | ||
+ | We used this protocol to transfer the construct in a new backbone. | ||
+ | |||
+ | ==Materials== | ||
+ | *PCR tubes | ||
+ | *dH20 | ||
+ | *Enzymes (EcoRI, PstI) | ||
+ | *BSA | ||
+ | *Enzyme Buffer (NEBuffer 2) | ||
+ | <br> | ||
+ | |||
+ | Note: All materials should be held on ice during preparation. | ||
+ | |||
+ | ==Protocol== | ||
+ | |||
+ | {| border="1" | ||
+ | !align="left"|sample | ||
+ | !align="right"|ul | ||
+ | |- | ||
+ | |DNA | ||
+ | |align="right"|10 | ||
+ | |- | ||
+ | |NEB buffer 2 | ||
+ | |align="right"|2 | ||
+ | |- | ||
+ | |BSA | ||
+ | |align="right"|0,5 | ||
+ | |- | ||
+ | |EcoRI | ||
+ | |align="right"|0,5 | ||
+ | |- | ||
+ | |PstI | ||
+ | |align="right"|1 | ||
+ | |- | ||
+ | |H2O | ||
+ | |align="right"|6 | ||
+ | |- style="font-style:italic;" | ||
+ | |Total | ||
+ | |align="right"|20 ul | ||
+ | |} | ||
+ | <br/> | ||
+ | |||
+ | |||
+ | 1. Incubate the restriction digest at 37C for 2 hours.<br> | ||
+ | 2. Incubate at 80C for 20min to heat kill the enzymes.<br> | ||
+ | 3. Store at -4C. | ||
+ | |||
+ | |||
+ | ==Double digest== | ||
+ | To check if the enzymes digest the plasmid as expected, the following digestion should be performed:<br> | ||
+ | 1. First use only EcoRI.<br> | ||
+ | 2. Incubate at 37 degrees Celsius for 1 hour.<br> | ||
+ | 3. take 1 ul of each sample.<br> | ||
+ | 4. add PstI to all the samples.<br> | ||
+ | 5. Incubate at 37 degrees Celsius for 1 hour.<br> | ||
+ | 6. take 1 ul of each sample.<br> | ||
+ | 7. take 1 ul of each undigested sample.<br> | ||
+ | 8. fill each of the three samples up to 10 ul including LD and check them on agarose gel.<br> | ||
{{:Team:Amsterdam/Footer}} | {{:Team:Amsterdam/Footer}} |
Revision as of 13:38, 13 September 2011
Contents |
Digestion: Making new constructs
We used this protocol for the digestion of the biobricks.
Materials
- PCR tubes
- dH20
- Enzymes (EcoRI, XbaI, SpeI, PstI)
- BSA
- Enzyme Buffer (NEBuffer 2)
Note: All materials should be held on ice during preparation.
Protocol
Vector | ul |
---|---|
DNA | 10 |
NEB buffer 2 | 2 |
BSA | 0,5 |
SpeI | 1 |
PstI | 1 |
H2O | 5,5 |
Total | 20 ul |
Insert | ul |
---|---|
DNA | 10 |
NEB buffer 2 | 2 |
BSA | 0,5 |
XbaI | 0,5 |
PstI | 1 |
H2O | 6 |
Total | 20 ul |
1. Incubate the restriction digest at 37C for 2 hours.
2. Incubate at 80C for 20min to heat kill the enzymes.
3. Store at -4C.
Double digest
To check if the enzymes digest the plasmid as expected, the following digestion should be performed:
1. First use only SpeI(vector) and XbaI(insert).
2. Incubate at 37 degrees Celsius for 1 hour.
3. take 1 ul of each sample.
4. add PstI to all the samples.
5. Incubate at 37 degrees Celsius for 1 hour.
6. take 1 ul of each sample.
7. take 1 ul of each undigested sample.
8. fill each of the three samples up to 10 ul including LD and check them on agarose gel.
Digestion: Changing the backbone
We used this protocol to transfer the construct in a new backbone.
Materials
- PCR tubes
- dH20
- Enzymes (EcoRI, PstI)
- BSA
- Enzyme Buffer (NEBuffer 2)
Note: All materials should be held on ice during preparation.
Protocol
sample | ul |
---|---|
DNA | 10 |
NEB buffer 2 | 2 |
BSA | 0,5 |
EcoRI | 0,5 |
PstI | 1 |
H2O | 6 |
Total | 20 ul |
1. Incubate the restriction digest at 37C for 2 hours.
2. Incubate at 80C for 20min to heat kill the enzymes.
3. Store at -4C.
Double digest
To check if the enzymes digest the plasmid as expected, the following digestion should be performed:
1. First use only EcoRI.
2. Incubate at 37 degrees Celsius for 1 hour.
3. take 1 ul of each sample.
4. add PstI to all the samples.
5. Incubate at 37 degrees Celsius for 1 hour.
6. take 1 ul of each sample.
7. take 1 ul of each undigested sample.
8. fill each of the three samples up to 10 ul including LD and check them on agarose gel.