- Designing and troubleshooting immunopanning protocols for purifying neural cells.
Designing and troubleshooting immunopanning protocols for purifying neural cells.
Cold Spring Harbor protocols (2014-12-03)
Ben A Barres
PMID25447277
ABSTRACT
Purifying and culturing cells from the central nervous system (CNS) has proved to be an incredibly powerful tool for dissecting fundamental neuron and glial properties, and especially powerful in understanding neuronal-glial interactions. In a series of detailed protocols, we have provided step-by-step instructions for purifying and culturing specific types of neurons, glia, and vascular cells from the CNS by immunopanning. This article discusses common pitfalls and errors as well as important design considerations for the immunopanning procedure.
MATERIALS
Product Number
Brand
Product Description
Sigma-Aldrich
Anti-Water Channel Aquaporin 4 antibody produced in rabbit, lyophilized powder, affinity isolated antibody
Sigma-Aldrich
Monoclonal Anti-Glial Fibrillary Acidic Protein (GFAP) antibody produced in mouse, clone G-A-5, ascites fluid
Sigma-Aldrich
Anti-Myelin Proteolipid Protein Antibody, CT, clone PLPC1, clone PLPC1, Chemicon®, from mouse
Sigma-Aldrich
Anti-Myelin Associated Glycoprotein Antibody, clone 513, clone 513, Chemicon®, from mouse