Abstract
Due to well-known limitations of in vivo and existing in vitro retinal models, a 3D in vitro model of the human retina that is reproducible and able to accurately
predict in vivo outcomes is highly desirable. Our aim was to investigate the consistency of human iPSC-derived retinal organoids (RO) produced at large scale by quantifying the gene and protein expression levels of key retinal cell markers across differentiation in multiple batches.
