Hi all,

I am having a problem performing an adhesion assay on retinoblastoma cells lines. Somehow, my cells are attaching to the well and glass coverslips without any adhesive substrate and I would like to know if there is anything I can do to limit this. My cells grow in suspension so should have minimal attachment.

I have found a protocol online which I have attached. The main difference is that I do not use blocking buffer as referred to in Step 6 - am I correct in thingking that this will prevent cell adherence to non-specific ligands?

Thanks in advance for your advice.

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