TY - CHAP
T1 - Immunostaining of the developing embryonic and larval Drosphila brain
AU - Diaper, Danielle C.
AU - Hirth, Frank
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Immunostaining is used to visualize the spatiotemporal expression pattern of developmental control genes that regulate the genesis and specification of the embryonic and larval brain of Drosophila. Immunostaining uses specific antibodies to mark expressed proteins and allows their localization to be traced throughout development. This method reveals insights into gene regulation, cell-type specification, neuron and glial differentiation, and posttranslational protein modifications underlying the patterning and specification of the maturing brain. Depending on the targeted protein, it is possible to visualize a multitude of regions of the Drosophila brain, such as small groups of neurons or glia, defined subcomponents of the brain’s axon scaffold, or pre- and postsynaptic structures of neurons. Thus, antibody probes that recognize defined tissues, cells, or subcellular structures like axons or synaptic terminals can be used as markers to identify and analyze phenotypes in mutant embryos and larvae. Several antibodies, combined with different labels, can be used concurrently to examine protein co-localization. This protocol spans over 3–4 days.
AB - Immunostaining is used to visualize the spatiotemporal expression pattern of developmental control genes that regulate the genesis and specification of the embryonic and larval brain of Drosophila. Immunostaining uses specific antibodies to mark expressed proteins and allows their localization to be traced throughout development. This method reveals insights into gene regulation, cell-type specification, neuron and glial differentiation, and posttranslational protein modifications underlying the patterning and specification of the maturing brain. Depending on the targeted protein, it is possible to visualize a multitude of regions of the Drosophila brain, such as small groups of neurons or glia, defined subcomponents of the brain’s axon scaffold, or pre- and postsynaptic structures of neurons. Thus, antibody probes that recognize defined tissues, cells, or subcellular structures like axons or synaptic terminals can be used as markers to identify and analyze phenotypes in mutant embryos and larvae. Several antibodies, combined with different labels, can be used concurrently to examine protein co-localization. This protocol spans over 3–4 days.
UR - http://www.scopus.com/inward/record.url?scp=84885622407&partnerID=8YFLogxK
U2 - 10.1007/978-1-62703-655-9_1
DO - 10.1007/978-1-62703-655-9_1
M3 - Chapter
C2 - 24048923
SN - 9781627036542
VL - 1082
T3 - Methods in Molecular Biology
SP - 3
EP - 17
BT - Methods in Molecular Biology
A2 - Sprecher, Simon G.
PB - Humana Press
CY - New York
ER -