No edit summary Tag: 2017 source edit |
Tag: 2017 source edit |
||
| Line 2: | Line 2: | ||
In this first workshop we learned and worked with algae cultivated in water based liquid. With few experiments and research we found out the requirements for them to grow. | In this first workshop we learned and worked with algae cultivated in water based liquid. With few experiments and research we found out the requirements for them to grow. | ||
<gallery> | |||
File:W1 p1.jpg | |||
File:W1 p2.jpg | |||
File:W1 p4.jpg | |||
File:W1 p3.jpg | |||
File:W1 p5.jpg | |||
File:W1 p6.jpg | |||
File:W1 p7.jpg | |||
</gallery> | |||
| Line 77: | Line 62: | ||
File:W2 p2.jpg | File:W2 p2.jpg | ||
File:W2 p3.jpg | File:W2 p3.jpg | ||
</gallery> | </gallery> | ||
[[File:W2 vid 1.mp4]] | |||
Revision as of 17:50, 14 September 2023
12.04.2023, 13.04.2023 - /Growing, Shaping and Living (with) Microalgae with biologist Johann
In this first workshop we learned and worked with algae cultivated in water based liquid. With few experiments and research we found out the requirements for them to grow.
28.04.2023, 29.04.2023 - /DNA analysis with molecular biologist Julian Chollet
For this workshop we focused on learning a molecular biology technique called PCR used to repeatedly replicate (amplify) a defined stretch of DNA for which the starting and ending nucleotide sequences are known. It is necessary to prepare samples (plants, flower, fruit, saliva, skin) of substances whose DNA we want to replicate and we do this through a process of mushing and mixing and centrifuging. After the peparation of the samples, we prepare the gel that need to contain them. Once pipeting the samples in the gel we wait for them to give results. Already after half an hour we can understand which samples contain DNA and in which the stretch of DNA is long or short.
