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Cy3 labeled telomere peptide nucleic acid probe

Manufactured by Panagene

The Cy3-labeled telomere peptide nucleic acid probe is a laboratory equipment used for the detection and analysis of telomere regions in DNA samples. It consists of a peptide nucleic acid (PNA) molecule labeled with the Cy3 fluorescent dye. The core function of this probe is to hybridize with complementary telomeric DNA sequences, enabling the visualization and quantification of telomere lengths in various experimental applications.

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3 protocols using cy3 labeled telomere peptide nucleic acid probe

1

Metaphase Chromosomes Telomere Analysis

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For analysis of metaphase chromosomes, activated B cells were arrested with 100 ng/mL colcemid (Sigma) for 1 hr prior to collection at each time point. This was followed by treatment with hypotonic solution (0.075 M KCl) and fixation with 3:1 methanol/acetic acid. Telomere-FISH analysis was performed with Cy3-labeled telomere peptide nucleic acid probe (Panagene). 50–55 images were analyzed per sample.
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2

Telomere-FISH Analysis of Activated B Cells

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Chromosomal aberrations of activated B cells were determined as previously described (24 (link)). Briefly, cells were arrested with 100 ng/mL colcemid (Sigma) for 1 h prior to collection at each time point. This was followed by treatment with hypotonic solution (0.075 M KCl) and fixation with 3:1 methanol/acetic acid. Telomere-FISH analysis was performed with Cy3-labeled telomere peptide nucleic acid probe (Panagene). 50–55 images were analyzed per sample.
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3

Metaphase Chromosomes Telomere Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
For analysis of metaphase chromosomes, activated B cells were arrested with 100 ng/mL colcemid (Sigma) for 1 hr prior to collection at each time point. This was followed by treatment with hypotonic solution (0.075 M KCl) and fixation with 3:1 methanol/acetic acid. Telomere-FISH analysis was performed with Cy3-labeled telomere peptide nucleic acid probe (Panagene). 50–55 images were analyzed per sample.
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