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The specificity of EBP2 antibody was confirmed by IF and IHC analysis (Supplementary Figure S4).
M9M was detected by IF performed with 9E10 antibodies, which recognize the Myc epitope.
Finally, we tested their ability to interact with microtubules in cells by IF.
This could be done by IF, but ChIPseq would be better.
We determined the subcellular localization of Myomegalin in RPE1 cells by IF.
Results obtained by IF were further documented in CHO cells by co-immunoprecipitations (IP) experiments.
Quantitation of Her2 and pHer2 by IF is feasible in FFPE breast tumor specimens.
Despite the apparent increase by IF, H3K9me3 levels were comparable between mutants and parental cells.
Crabp1 expression was also examined within mammary tissues from different developmental stages by IF.
Upon infection with rickettsiae, ANG was induced, as visualized by IF.
VIM expression was not detected in MCF7-siTFF3 cells by IF.
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