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Bx60 epifluorescence microscope

Manufactured by MetaSystems

The BX60 epifluorescence microscope is a high-performance optical instrument designed for fluorescence imaging applications. It features a sturdy, ergonomic design and delivers clear, high-resolution images. The microscope is equipped with a range of illumination options and filter sets to accommodate various fluorescent dyes and probes. Its core function is to enable researchers and scientists to visualize and analyze fluorescently labeled samples with precision and efficiency.

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2 protocols using bx60 epifluorescence microscope

1

Fluorescence Microscopy for Haplotype Detection

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Analyses were performed using an Olympus BX60 epifluorescence microscope equipped with an Isis Imaging System (Metasystems). Only those signal combinations with a clear distribution of two clustered signals (in close proximity or overlapping) and one separated signal were considered informative. The distant signal must be separated from the two others by at least a two-fold longer distance compared with the separation of the clustered signals. This probe configuration allowed us to distinguish the normal haplotype (N) and the 3 Mb inversion haplotype (inv) (Fig. 1C and E). A minimum of 100 informative signal combinations were analysed per sample. Metaphase chromosomes were also observed to test probe specificity.
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2

Fiber-FISH Analysis of Genomic Loci

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A minimum of 20 informative fibers were scored for every single probe combination on an Olympus BX60 epifluorescence microscope equipped with Isis Imaging System (Metasystems). Fiber-FISH analyses were developed by applying the following assessment criteria adapted from Molina et al.50 (link): (i) at least three signals of different colour combinations must be observed in a consecutive and linear fashion, ii) two or more signals of the same colour are considered independent when they are separated by a distance twice the distance of every single bead-on-string, and iii) signals are considered informative regardless of the size (Fig. 1D). For each BAC and fosmid combination, we scored the frequency of the fosmid signal numbers that corresponded to the tandem sequence blocks.
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