"
Team:Peking S/lab/protocol
From 2011.igem.org
(Difference between revisions)
(→Peking S 2011) |
(→DNA Double Digestion Protocol) |
||
| (5 intermediate revisions not shown) | |||
| Line 1: | Line 1: | ||
| - | |||
__NOTOC__ | __NOTOC__ | ||
| - | {{Template:Http://2011.igem.org/Team:Peking_S/ | + | {{Template:Http://2011.igem.org/Team:Peking_S/box4lab}} |
{{Template:Http://2011.igem.org/Team:Peking S/background}} | {{Template:Http://2011.igem.org/Team:Peking S/background}} | ||
| + | |||
| + | |||
| Line 9: | Line 10: | ||
| - | + | {{Template:Http://2011.igem.org/Team:Peking S/protocal}} | |
| + | |||
| + | =DNA Double Digestion Protocol= | ||
<html> | <html> | ||
| + | <a href="https://static.igem.org/mediawiki/2010/8/84/DNA_double_digestion_protocol.pdf"target="blank"><img src="https://static.igem.org/mediawiki/2010/9/91/PKU_Adobe_Reader_Logo.jpg" width=20>download PDF version</a><br> | ||
| + | </html> | ||
| + | ==Materials:== | ||
| + | *DNA sample(s) in water or TE buffer | ||
| + | |||
| + | *10x digestion buffer | ||
| + | |||
| + | *Restriction enzymes (EcoRI or SpeI or XbaI or PstI) | ||
| + | |||
| + | *DNA loading buffer (if electrophoresis is subsequent) | ||
| + | |||
| + | *Agarose gel 1.5% (or different depending on expected band sizes) | ||
| + | |||
| + | |||
| + | ==Procedure:== | ||
| + | 1. Test the concentration of the DNA sample(s). | ||
| + | |||
| + | 2. Pipet the following into a microfuge tube: | ||
| + | |||
| + | 20uL reaction system 50uL reaction system | ||
| + | |||
| + | DNA around 1ug around 2.5ug | ||
| + | |||
| + | 10x Digestion buffer 2uL 5uL | ||
| + | |||
| + | 1st Enzyme 1-1.5uL 2.5-4uL | ||
| - | + | 2ndEnzyme 1-1.5uL 2.5-4uL | |
| - | + | ||
| - | + | ||
| - | + | ddWater Rest of volume Rest of volume | |
| - | + | ||
| - | + | ||
| - | + | 3. Incubate at recommended temperature (37.0 degrees) for 2 or 4 hours (0.5~2hfor enzymes of NEB, 4h for enzymes of Takara). | |
| - | + | ||
| - | + | ||
| - | + | 4. Take 2 to 5 uLof the digested sample, add loading buffer, and run it on the | |
| - | + | agarose gel to check the result, or take the entire sample to run to extract a | |
| - | + | wanted fragment). | |
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | + | ==Tips:== | |
| - | + | 1. DNA: | |
| - | + | ||
| - | + | *For identification of DNA, use 0.4 ug/uL DNA; (or 2uL from a nice DNA mini prep) | |
| - | + | ||
| - | + | ||
| - | + | *For cloning, 1ug/uL DNA is enough. | |
| - | + | ||
| - | + | ||
| - | + | 2. Buffer: we’d better use the buffer that comes with the enzyme, which | |
| - | + | means buffers from other company may cause some abnormal results. | |
| - | + | ||
| - | + | 3. Enzyme: the maximum volume that an enzyme can be used is 1/10 of the | |
| - | + | total reaction volume (example: 2 uL for 20 uL reaction system). If you want to do overnight digestion, add less enzyme (example: 1 uL for 20 uL reaction | |
| - | + | system). It is necessary to point that too many enzymes will reduce the efficiency of enzyme digestion with glycerol in it. | |
| - | + | 4. Gel: make sure to run the uncut DNA as a control along with the digested | |
| + | DNA sample(s). And, always run a DNA marker! | ||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | + | ==References:== | |
| + | *Current protocols in molecular biology (3.1.1-3.1.2) | ||
Latest revision as of 08:31, 2 October 2011
Template:Https://2011.igem.org/Team:Peking S/bannerhidden
Template:Https://2011.igem.org/Team:Peking S/bannerhidden
Protocol
Double Digestion |Gel Extraction|Miniprep | Chemical Inducible Expression of GFP |DNA Purification |Ligation of Insert DNA | PCR |Preparation of Competent Cells| Site-directed Mutagenesis| Transformation|
DNA Double Digestion Protocol
download PDF versionMaterials:
- DNA sample(s) in water or TE buffer
- 10x digestion buffer
- Restriction enzymes (EcoRI or SpeI or XbaI or PstI)
- DNA loading buffer (if electrophoresis is subsequent)
- Agarose gel 1.5% (or different depending on expected band sizes)
Procedure:
1. Test the concentration of the DNA sample(s).
2. Pipet the following into a microfuge tube:
20uL reaction system 50uL reaction system
DNA around 1ug around 2.5ug
10x Digestion buffer 2uL 5uL
1st Enzyme 1-1.5uL 2.5-4uL
2ndEnzyme 1-1.5uL 2.5-4uL
ddWater Rest of volume Rest of volume
3. Incubate at recommended temperature (37.0 degrees) for 2 or 4 hours (0.5~2hfor enzymes of NEB, 4h for enzymes of Takara).
4. Take 2 to 5 uLof the digested sample, add loading buffer, and run it on the agarose gel to check the result, or take the entire sample to run to extract a wanted fragment).
Tips:
1. DNA:
- For identification of DNA, use 0.4 ug/uL DNA; (or 2uL from a nice DNA mini prep)
- For cloning, 1ug/uL DNA is enough.
2. Buffer: we’d better use the buffer that comes with the enzyme, which means buffers from other company may cause some abnormal results.
3. Enzyme: the maximum volume that an enzyme can be used is 1/10 of the total reaction volume (example: 2 uL for 20 uL reaction system). If you want to do overnight digestion, add less enzyme (example: 1 uL for 20 uL reaction system). It is necessary to point that too many enzymes will reduce the efficiency of enzyme digestion with glycerol in it.
4. Gel: make sure to run the uncut DNA as a control along with the digested DNA sample(s). And, always run a DNA marker!
References:
- Current protocols in molecular biology (3.1.1-3.1.2)
