Wiki/Team:Warsaw/protocols

Lab protocols

introduction

Here is the place for the all protocols used by the Warsaw Team during the iGEM 2009. Feel free to add yours.

Please be sure to use the

{{Anchor|name of protocol}}

tag before your desired protocol - it simplifies further linking to the protocols in notebook entries (then you will use just

[https://2009.igem.org/Team:Warsaw/protocols#protocol_name protocol name]

to link to your protocol. You can also put the whole name of protocol (as it's used to define the header of desired protocol) after the # sign (so you can just copy the link from the automatically generated table of contents in the top of page) but in my opinion it's simpler to define shorter/simpler names for linking

A great example of describing protocols you can find on the iGEM 2008 Warsaw Team page

Examples:

Protocols of the P. Group

Chemotransformation

Add desired volume of DNA to the 100-μl-culture in eppendorf tube. Incubate 30 min on ice. Heat shock for 90 s at 42°C. Incubate 10 min on ice. Add 0.9 ml of culture medium and let the bacteria grow at 37°C.

Plasmid DNA isolation

We use "Plasmid Mini" plasmid DNA isolation kit from A&A Biotechnology and follow the protocol of producer.

DNA isolation from agarose gel

We use "Gel-Out" DNA isolation kit from A&A Biotechnology and follow the protocol of producer.

Protocols of the M. Group

DNA purification after enzymatic reaction

We use "Clean-Up" DNA purification kit from A&A Biotechnology and follow the protocol of producer.

Genomic DNA isolation

We use "Genomic-Mini" universal genomic DNA isolation kit from A&A Biotechnology and follow the protocol of producer.

DNA digest

We use restriction enzymes and buffers provided by Fermentas. Overall volume of digest mix is either 20 μl, either 50 μl in case of digesting for ligation. We usually use 1 μl of restriction enzyme and the buffer in 10x dilution (as they initially are 10x concentrated). The rest of mix is plasmid DNA.