Figure 1.
Figure 1. Representative laser scanning confocal microscopy images obtained after applying a 2-phase combined FISH technique based on coordinate assembly protocol for assessment of TL within the same CP CML patient’s CD34+38− compartment. (A) In phase 1, BCR-ABL+ and BCR-ABL− cells were identified by BCR-ABL FISH staining. (B) In phase 2, PNA-Tel Q-FISH is used to restain the samples allowing telomere quantification in the BCR-ABL+ and BCR-ABL− cells within the same individual’s CD34+38− compartment. Image magnification ×630. Digital zoom ×2.5. DAPI, 4′,6-diamidino-2-phenylindole.

Representative laser scanning confocal microscopy images obtained after applying a 2-phase combined FISH technique based on coordinate assembly protocol for assessment of TL within the same CP CML patient’s CD34+38compartment. (A) In phase 1, BCR-ABL+ and BCR-ABL cells were identified by BCR-ABL FISH staining. (B) In phase 2, PNA-Tel Q-FISH is used to restain the samples allowing telomere quantification in the BCR-ABL+ and BCR-ABL cells within the same individual’s CD34+38 compartment. Image magnification ×630. Digital zoom ×2.5. DAPI, 4′,6-diamidino-2-phenylindole.

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