9 Matching Annotations
  1. Oct 2023
    1. Die Bewegung gegen die Autobahn A69, zu der auch Extinction Rebellion gehört, organisiert in einem Ort namens La Crémade eine ZAD (Zone à défendre, zu verteidigende Gebiet). Dazu wurden für den Autobahnbau bereits enteignete Gebäude besetzt, obwohl die Exekutive die Dächer beseitigt und großflächig Mist verstreut hatte, um die Aktivist:innen abzuschrecken. Die Exekutive vertrieb die Protestierenden gewaltsam. Reportage in der Libération. https://www.liberation.fr/environnement/a69-les-gendarmes-mobiles-tentent-de-demanteler-la-zad-des-opposants-20231022_YHXQJTFNOBAMBESFWFPXBWSG7Y/

  2. Oct 2022
    1. Sometimes a Scrum Team is hired and assembled fully by an organization without any input from the Scrum Team members, and there's nothing in Scrum preventing that. Likewise, there is nothing in Scrum that prevents a group of people from forming their own Scrum Team and organizing themselves into a structure that gives them their best shot at achieving the organization's goals.

      the Scrum Team may be both assembled or self-assembled

    2. In Scrum, the Product Owner manages the Product Backlog, Scrum Masters manage Scrum's effectiveness, and Developers manage how Increments are created.

      this is important, who is accountable for the management of what

    1. who

      is it really about who (customer/user) we're working for? or can we say that it's about what (goal/value/outcome /impact) we're working for?

  3. May 2019
    1. Inverse PCR is a technique to amplify unknown regions flanking the site of transposon insertion using the primers designed from the known sequence from one end of the transposon element. Genomic DNA was digested with a 4-base recognition restriction enzyme, Sau3A1 followed by intramolecular ligation set up at high dilutions. These ligated molecules were then used as templates for the PCR performed with a pair of divergently-oriented primers designed from one end of the transposon named AH1-AH2. The PCR product thus obtained was sequenced with the same set of primers to identify the junction sequence at the site of transposon insertion and hence the identity of the gene disrupted in each case. Typical PCR conditions used were as follows:- Annealing 55°C 2 min Elongation 72°C (1 min/kb of DNA template to be amplified) Denaturation 95°C 2 min After 30 cycles of PCR, the final elongation step was carried out again for 10 min at 72°C
    2. Inverse PCR
  4. Oct 2016