Dear All,

We are currently working on endometrial cancer organoids. We find that when passaging our organoids (in domes of BME/Matrigel), we lose a significant amount due to them sticking to our 15ml falcon tubes (we can see them stuck to the tubes under the microscope). We have used BSA 1% and BSA 5% pre-coating as well as low binding tips and tubes to try and resolve this problem.

Does anyone have any suggestions on how to lower the amount of organoids lost during passages? These are primary organoids coming from fresh patient samples that have not been frozen.

Looking forward to your comments.

Thank you for your time and help. Regards

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