RAT ANTI C-MYC

Published customer image:
Rat anti c-myc antibody, clone JAC6 (MCA1929) used for the detection of c-myc tagged APP by immunofluorescence.
Image caption:
APP processing deficient mutants show stronger synaptogenic activity than APPwt. The synaptogenic activity of APP was analyzed in a co-culture assay. HEK293 cells were transiently transfected with APPwt and seeded 24 h later on primary cortical neurons (DIV7). The cells were fixed after 24 h (neurons DIV 8) and analyzed via immunocytochemistry. (A) Cells were stained with TAU1 as axonal marker, Synaptophysin as presynaptic marker and antibody c-myc for APP.

From: Stahl R, Schilling S, Soba P, et al.
Shedding of APP limits its synaptogenic activity and cell adhesion properties.
.
doi:10.3389/fncel.2014.00410
This image is from an open access article distributed under terms of a.

Published customer image:
Rat anti c-myc antibody, clone JAC6 (MCA1929) used for the detection of c-myc tagged APP by immunofluorescence.
Image caption:
APP processing deficient mutants show stronger synaptogenic activity than APPwt. The synaptogenic activity of APP was analyzed in a co-culture assay. HEK293 cells were transiently transfected with APPwt and seeded 24 h later on primary cortical neurons (DIV7). The cells were fixed after 24 h (neurons DIV 8) and analyzed via immunocytochemistry. (A) Cells were stained with TAU1 as axonal marker, Synaptophysin as presynaptic marker and antibody c-myc for APP.

From: Stahl R, Schilling S, Soba P, et al.
Shedding of APP limits its synaptogenic activity and cell adhesion properties.
Front Cell Neurosci. 2014;8:410.
doi:10.3389/fncel.2014.00410
This image is from an open access article distributed under terms of a Creative Commons Attribution License.

Published customer image:
Rat anti c-myc antibody, clone JAC6 (MCA1929) used for the detection of c-myc tagged APP by immunofluorescence.
Image caption:
APP processing deficient mutants show stronger synaptogenic activity than APPwt. The synaptogenic activity of APP was analyzed in a co-culture assay. HEK293 cells were transiently transfected with APPwt and seeded 24 h later on primary cortical neurons (DIV7). The cells were fixed after 24 h (neurons DIV 8) and analyzed via immunocytochemistry. (A) Cells were stained with TAU1 as axonal marker, Synaptophysin as presynaptic marker and antibody c-myc for APP.

From: Stahl R, Schilling S, Soba P, et al.
Shedding of APP limits its synaptogenic activity and cell adhesion properties.
Front Cell Neurosci. 2014;8:410.
doi:10.3389/fncel.2014.00410
This image is from an open access article distributed under terms of a Creative Commons Attribution License.