Application
GFAP antibody detects GFAP protein expression in astrocytes and Tuj1 antibody detects Tuj1 protein expression in neurons by immunofluorescent analysis. Sample:Cultured rat E18 primary cortical neurons and astrocytes, DIV 8. Cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: GFAP protein stained by GFAP antibody diluted at 1:250. Red: beta Tubulin 3/ TUJ1, stained by beta Tubulin 3/ TUJ1 antibody [GT11710] diluted at 1:250. Blue: Fluoroshield with DAPI .
Application
GFAP antibody detects GFAP protein expression by immunofluorescent analysis. Sample:Cultured rat E18 primary cortical neuron, DIV 8 cells were fixed in 4% paraformaldehyde at RT for 15 min. Red: GFAP protein stained by GFAP antibody diluted at 1:250. Green: Glutamine synthetase, stained by Glutamine synthetase antibody [GT7711] diluted at 1:250. Blue: Fluoroshield with DAPI .
Application
Immunocytochemistry/Immunofluorescence: GFAP Antibody - Rat neurons stained with Neurofilament Heavy antibody (red) and GFAP antibody (green).
Application
Immunocytochemistry/Immunofluorescence: GFAP Antibody - Mixed neuron-glial cultures stained with GFAP antibody (red) and Vimentin antibody (green). The fibroblastic cells contain only Vimentin and so are green. The astrocytes contain either Vimentin and GFAP (appearing golden) or predominantly GFAP (appearing red). Blue is nuclear DNA stain.
Application
Western Blot: GFAP Antibody - Western blot analysis of GFAP expression in whole rat cerebellum homogenate using
WB
The summary graphs (b) showing GFAP filament/fiber length and fluorescence intensity of CBS-positive cells in ventral glial lamina (VGL, c). (B–C) Representative Western blot bands (a) and the summary graphs (b) showing GFAP fragments (B, n = 5) and CBS (C, n = 7), respectively.
WB
(A) Western blot bands (a) and the summary graph
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(b) showing the expression of GFAP in the SON of brain slices (n = 6) with CTR, AOA, OT, and AOA plus OT, respectively.