diff --git a/src/data/hptimelinedata.tsx b/src/data/hptimelinedata.tsx index 523ef98984bd3781ca14e30f4f1f63b005a4c192..ea63fc01caaae0349c59c1896f909fc1885f4872 100644 --- a/src/data/hptimelinedata.tsx +++ b/src/data/hptimelinedata.tsx @@ -567,7 +567,35 @@ export const timelinedata: Array<TimelineDatenpunkt> = [ quote: "The use of primary cultures in research represents the first step toward clinical studies. Your approach is innovative, as we have never undertaken something like this before.", aimofcontact: "Our primary goal in reaching out to her was to gain insights into optimizing cell culture media, explore potential sponsorship opportunities for our project, and seek expert advice on handling primary cells in the lab.", insights: "Throughout our multiple discussions, she offered detailed advice on selecting and optimizing cell culture media for our specific needs, while also connecting us with opportunities for sponsorship. Later in the project, she provided technical guidance on the cultivation and handling of primary cells, ensuring that we followed best practices for cell culture.", - implementation: "Based on her feedback, we refined our approach to cell culture media, enhancing our experimental workflows.Her technical support, as well as the support of Julia Watson helped us to establish our experiments in cellculture. Additionally, her advice was critical during the transition to primary cell culture, helping us secure the necessary resources and expertise for our experiments.", + implementation: [<p>Based on her feedback, we refined our approach to cell culture media, enhancing our experimental workflows.Her technical support, as well as the support of Julia Watson helped us to establish our experiments in cellculture. Additionally, her advice was critical during the transition to primary cell culture, helping us secure the necessary resources and expertise for our experiments. + <br></br> + <br></br> + <br></br> + <div className="row" style={{ display: "flex", justifyContent: "space-between", gap: "10px" }}> + <div className="col" style={{ flex: "1" }}> + <iframe + title="Bielefeld-CeBiTec: Air-liquid interface (ALI) culture of human nasal epithelial cells (hNECs) (2024)" + width="100%" + height="315" + src="https://video.igem.org/videos/embed/52424a62-745a-454b-bff6-d61a13a5f967" + frameBorder="0" + sandbox="allow-same-origin allow-scripts allow-popups allow-forms"> + </iframe> + <p>An air-liquid interface culture of human nasal epithelial cells, which have undergone differentiation into ciliated epithelium, may be employed as an example. The formation of ciliated epithelium is evident from the 'flickering'. This phenomenon involves the rhythmic movement of numerous cilia. Additionally, the uniform direction and tempo of cell debris movement, in contrast to the random movement observed in the absence of ciliated epithelium, provides further evidence of its presence.</p> + </div> + <div className="col" style={{ flex: "1" }}> + <iframe + title="Bielefeld-CeBiTec: Apical-out airway organoids (AOAO) culture D19 (2024)" + width="100%" + height="315" + src="https://video.igem.org/videos/embed/e70674d7-9f18-4ab5-b0ec-16a7801d01cd" + frameBorder="0" + sandbox="allow-same-origin allow-scripts allow-popups allow-forms"> + </iframe> + <p>Apical-Out Airway Organoid (AOAO) culture D19: Visible apical-out airway organoids in action. These 3D structures, which mimic the airway epithelium, allow detailed study of cellular processes such as mucociliary transport and secretory activities, in which cilia and vesicles play a key role.</p> + </div> + </div> + </p>], summary: "We have had the privilege of collaborating with a dedicated expert from Stemcell Technologies, who has consistently supported iGEM Bielefeld. She provided valuable guidance on cell culture media, sponsorship opportunities, and later, practical advice for cultivating primary cells. Her contributions have been instrumental in advancing our project.", months: "several times", pictureurl_interview: "https://static.igem.wiki/teams/5247/photos/hp/daniela.webp",