Hi all,
In most cases people throw away microfluidic chips that are being used for single cell RNA-seq, as the fear for cross contamination exists.
I was wondering, why is it so hard to clean and reuse them? And does anyone know a good protocol or paper for cleaning those chips that works? I think that if they can be cleaned successfully, it will save many groups some costs.
Thanks!
Edit: Even though it is not directly a Bioinformatics question, I guess that it are mainly Bioinformaticians who would know about this.
I don't think this is a bioinformatics question. It might be closed.
Yes, but there is no better place to ask this, as it are mainly Bioinformaticians who would design such experiments.