PLA labeled cells were imaged on a confocal microscope (Zeiss 510 META, Carl Zeiss, Jena, Germany). Z-stacks were acquired to allow for three-dimensional rendering in Volocity software (Perkin Elmer, Waltham, MA). DAPI fluorescence images were processed in the EBImage package or the R statistical programming environment to better define the nuclear boundary. Differential Interference Contrast data from brightfield images were processed in Photoshop (Adobe, San Jose, CA) using high pass filtering and median filtering to allow for rough visualization of cell boundaries. No processing was done to PLA fluorescence. All images were handled equivalently in Volocity, they were rendered in “3D Opacity” mode and channel opacity, density and black levels were all set to the same between images. Each square in the grid is approximately 22 μm on a side.
Anti h2a z antibody
The Anti-H2A.Z antibody is a tool used in molecular biology research to detect and analyze the H2A.Z histone variant. H2A.Z is a key component of chromatin and plays a role in regulating gene expression. The antibody can be used in various techniques such as Western blotting, immunohistochemistry, and immunoprecipitation to study the localization and abundance of H2A.Z within cellular samples.
Lab products found in correlation
2 protocols using anti h2a z antibody
Proximity Ligation Assay for GLI1 and H2A.Z
PLA labeled cells were imaged on a confocal microscope (Zeiss 510 META, Carl Zeiss, Jena, Germany). Z-stacks were acquired to allow for three-dimensional rendering in Volocity software (Perkin Elmer, Waltham, MA). DAPI fluorescence images were processed in the EBImage package or the R statistical programming environment to better define the nuclear boundary. Differential Interference Contrast data from brightfield images were processed in Photoshop (Adobe, San Jose, CA) using high pass filtering and median filtering to allow for rough visualization of cell boundaries. No processing was done to PLA fluorescence. All images were handled equivalently in Volocity, they were rendered in “3D Opacity” mode and channel opacity, density and black levels were all set to the same between images. Each square in the grid is approximately 22 μm on a side.
Proximity Ligation Assay for GLI1 and H2A.Z
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