We are trying to harvest and culture mouse primary nodose/jugular neurons. My isolation technique is good as I learned from Bradley Undem's lab. However, when I plate the cell suspension I get very few cells and they seem to detach. I am pooling 4 ganglia together.

Any tips on digestion (currently using papain first, then collagenase IV and dispase II), trituration and plating? Any suggestions welcome. Thx

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