From 8c2f1d01433f7a86494ab974d8bc597355ea44a0 Mon Sep 17 00:00:00 2001
From: Isabell Guckes <isabell.guckes@uni-bielefeld.de>
Date: Fri, 27 Sep 2024 01:17:58 +0200
Subject: [PATCH] fett again
---
src/contents/methods.tsx | 1 +
1 file changed, 1 insertion(+)
diff --git a/src/contents/methods.tsx b/src/contents/methods.tsx
index a71bb299..b9692eab 100644
--- a/src/contents/methods.tsx
+++ b/src/contents/methods.tsx
@@ -22,6 +22,7 @@ export function Methods() {
<figcaption>microscopic recording of micropipette sealing of a HEK293 cell </figcaption>
</figure>
+
<p>The success of patch clamp experiments heavily depends on the composition of the solutions used. Typically, two main types of solutions are employed: The <strong>Pipette Solution</strong> in the micropipette mimics the intracellular environments, while the <strong>Bath Solution</strong> surrounds the cell and usually contains components that replicate the extracellular environment. Both solutions are meticulously designed to reflect the physiological conditions under which the cells operate, thereby ensuring that the measurements accurately reflect ion channel activity in a natural setting [2].</p>
<figure>
<img src="https://static.igem.wiki/teams/5247/photos/for-wiki-texts/meth-patch-clamp/bild-meth-patch-clamp.png" alt="Patch clamp setup"/>
--
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