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CYTOGENETICS: Cancer FCPE FISH Cytogenetics and Molecular Pathology Laboratory Sample drop-off locations: Office use only Children's Hospital One child's Place Central Receiving 2N25 St. Louis, MO
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Step 1: Start by wearing appropriate personal protective equipment (PPE) such as gloves, lab coat, and safety eyewear.
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Step 2: Prepare the cytogenetics cancer FFPE (Formalin-Fixed Paraffin-Embedded) tissue specimen by cutting thin sections from the block.
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Step 3: Deparaffinize the tissue sections by treating them with xylene or other suitable deparaffinization reagents. This will remove the paraffin wax and expose the tissue.
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Step 4: Rehydrate the tissue sections by soaking them in a series of decreasing concentrations of alcohol (e.g., 100%, 95%, 70%) to remove any remaining xylene or deparaffinization reagents.
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Step 5: Perform a pretreatment step if required, such as antigen retrieval or protease digestion, to enhance the accessibility of the target DNA or RNA in the tissue sections.
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Step 6: Prepare the probe mixture by combining the fluorescently labeled DNA probes specific to the chromosomal regions of interest with a hybridization buffer.
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Step 7: Apply the probe mixture onto the tissue sections and cover them with a coverslip. Incubate the sections in a humidified chamber at an appropriate temperature for the probes to hybridize to the target DNA or RNA sequences.
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Step 8: After the hybridization is complete, remove the coverslip and wash the tissue sections to remove any unbound probes.
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Step 9: Counterstain the nuclei with a DNA stain, such as DAPI (4',6-diamidino-2-phenylindole), to visualize the cellular morphology.
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Step 10: Mount the tissue sections onto glass slides using a mounting medium and cover them with a coverslip. Allow the slides to dry before analysis.
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Step 11: Examine the slides using a fluorescence microscope equipped with appropriate filters to visualize the fluorescent signals from the labeled probes.
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Step 12: Analyze the cytogenetic abnormalities, such as chromosomal rearrangements or gene amplifications, by observing the patterns and intensity of the fluorescent signals.
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Step 13: Document and interpret the results based on established guidelines and standards in cytogenetics.
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Step 14: Prepare a comprehensive report summarizing the findings and providing an interpretation of the cytogenetic abnormalities detected.

Who needs cytogenetics cancer ffpe fish?

01
Patients with suspected or diagnosed cancer may require cytogenetics cancer FFPE FISH for further evaluation and characterization of their tumor.
02
Oncologists, pathologists, and other healthcare professionals involved in cancer diagnosis, treatment, and research may rely on cytogenetics cancer FFPE FISH to guide patient management.
03
Researchers studying cancer genetics and the underlying chromosomal abnormalities may utilize cytogenetics cancer FFPE FISH to investigate specific genetic markers or gene rearrangements.
04
Clinical laboratories performing molecular genetic testing for cancer may offer cytogenetics cancer FFPE FISH as part of their test menu to aid in the diagnosis or prognosis of cancer patients.
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Cytogenetics cancer FFPE FISH is a technique used to detect genetic abnormalities in cancer cells using formalin-fixed paraffin-embedded tissue samples.
Cytogenetics cancer FFPE FISH must be carried out by trained professionals in the field of molecular genetics and pathology.
To fill out cytogenetics cancer FFPE FISH, the technician must follow a standardized procedure involving tissue processing, hybridization, and imaging.
The purpose of cytogenetics cancer FFPE FISH is to identify specific genetic mutations or rearrangements that may be driving the development of cancer.
The report for cytogenetics cancer FFPE FISH should include details on the genetic abnormalities detected, their clinical significance, and recommendations for patient management.
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