SHEEP ANTI RAT TGN38

Published customer image:
Sheep anti Rat TGN38 antibody (AHP499) used for identification of the trans-golgi network in mouse embryonic fibroblasts by immunofluorescence.
Image caption:
Phosphorylated TBK1 is localized to the TGN in ISD-stimulated primary MEFs. a, Immunostaining of phosphorylated TBK1 (red) in cells treated with nocodazole and ISD. GM130 (a CGN protein, cyan) and TGN46 (a TGN protein, magenta) were co-stained. Scale bars, 10 μm. b-c, The mini-Golgi stacks indicated by the boxes in (a) were magnified. The cis and trans-regions of the mini-Golgi stacks were outlined with dashed line.

From: Mukai, K. et al. 2016.
Activation of STING required Palmtoylation oat the Golgi.
Nat Comms article 11932.
This image is from an open access article distributed under terms of a.

Published customer image:
Sheep anti Rat TGN38 antibody (AHP499) used for identification of the trans-golgi network in mouse embryonic fibroblasts by immunofluorescence.
Image caption:
Phosphorylated TBK1 is localized to the TGN in ISD-stimulated primary MEFs. a, Immunostaining of phosphorylated TBK1 (red) in cells treated with nocodazole and ISD. GM130 (a CGN protein, cyan) and TGN46 (a TGN protein, magenta) were co-stained. Scale bars, 10 μm. b-c, The mini-Golgi stacks indicated by the boxes in (a) were magnified. The cis and trans-regions of the mini-Golgi stacks were outlined with dashed line.

From: Mukai, K. et al. 2016.
Activation of STING required Palmtoylation oat the Golgi.
Nat Comms article 11932.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.

Published customer image:
Sheep anti Rat TGN38 antibody (AHP499) used for identification of the trans-golgi network in mouse embryonic fibroblasts by immunofluorescence.
Image caption:
Phosphorylated TBK1 is localized to the TGN in ISD-stimulated primary MEFs. a, Immunostaining of phosphorylated TBK1 (red) in cells treated with nocodazole and ISD. GM130 (a CGN protein, cyan) and TGN46 (a TGN protein, magenta) were co-stained. Scale bars, 10 μm. b-c, The mini-Golgi stacks indicated by the boxes in (a) were magnified. The cis and trans-regions of the mini-Golgi stacks were outlined with dashed line.

From: Mukai, K. et al. 2016.
Activation of STING required Palmtoylation oat the Golgi.
Nat Comms article 11932.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.