BioRender Template

Gs vs Gi/o GPCR Signaling

Created by 
Kassidy Jungles
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Description: This template compares Gs and Gi/o G-protein coupled receptor signaling at the plasma membrane, showing how the Gs alpha subunit activates adenylyl cyclase to convert ATP into cAMP. In contrast, the Gi/o alpha subunit inhibits adenylyl cyclase, reducing cAMP production, as indicated by the plus and minus symbols on each side.

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BioRender Template FAQs

What does the Gs vs Gi/o GPCR Signaling template show?

This template compares Gs and Gi/o G-protein coupled receptor signaling at the plasma membrane, showing how the Gs alpha subunit activates adenylyl cyclase to convert ATP into cAMP. In contrast, the Gi/o alpha subunit inhibits adenylyl cyclase, reducing cAMP production, as indicated by the plus and minus symbols on each side.

Is the Gs vs Gi/o GPCR Signaling template free to use?

Yes, you can customize this template with a free BioRender account (no credit card required). Paid plans unlock additional export formats, higher-resolution downloads, and publication permissions.

Can I edit or customize this template?

Yes, every element is fully editable. Icons, labels, colors, arrows, shapes and layout can all be changed to match your preferences or needs using BioRender's drag-and-drop editor. You can add or remove elements to fully customize your use case.

Is this template accepted for use in journals, theses, or grant applications?

Yes, BioRender icons and templates meet journal, grant, and copyright standards for publication, and many researchers cite BioRender directly in their figure legends.

How do I cite BioRender if I use this template?

Unlock publication permissions with a paid plan, and include 'Created with BioRender.com' in your figure legend, or cite BioRender directly per your journal's guidelines.

What is Gs vs Gi/o GPCR Signaling used for / who typically uses this template?

Researchers and scientists use this template for publications, funding proposals, grant applications, presentations, posters, and more.