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Oncology


Test Name: Chromosome 1p/19q Deletion Detection
Compliance:CE-IVD
Test Description:Combined loss of chromosomal arms 1p and 19q resulting from an unbalanced t(1;19)(q10;p10) translocation leads to the loss of one hybrid chromosome and thus loss of heterozygosity. This cytogenetic aberration is strongly associated with oligodendrogliomas. This test aims to identify co-deletion of the chromosome 1p/19q in oligodendrogliomas patients.
Methodology:Fluorescent in Situ Hybridization (FISH) Analysis
Gene Name:
Protein Name:
Specimen Requirements:FFPE Slides: 5-10 4µm FFPE tissue unstained sections on coated slides. One section must be stained with H&E and mounted with tumor region (area of interest) marked. Please include a copy of corresponding surgical pathology report. FFPE Block: Paraffin-embedded, formalin-fixed tissue block containing adequate amounts of tumor to be analyzed with areas of tumor marked. Please include a copy of corresponding surgical pathology report.
Storage Condition:Room Temperature
Turn Around Time:3-5 working days from day of specimen received
OMIM:
Genetic Home Reference:
Phone:+852.2986.1270
Fax:+852.2527.7028
E-mail:contact@hk-mpdc.com
27/F., Strand 50, No.50 Bonham Strand, Sheung Wan, Hong Kong
Opening Hours
Mondays to Fridays: 09:00-18:00
Saturdays: 09:00-16:00
Sundays and Public Holidays: Closed

For specimen pickup arrangements, please phone +852.2986.1270




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