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Trisomy 12

DESCRIPTION – Trisomy 12 is the common cytogenetic abnormality and has various features including abnormal morphology and increased prevalence of NOTCH1 mutation

CLINICAL UTILITY – trisomy 12 is one of the most commonly reported chromosome aberration in B-cell chronic lymphocytic leukemia and is of prognostic importance. FISH analysis detects trisomy 12 in non-dividing cells which cannot be identified with routine cytogenetic studies

METHODOLOGY – fluorescence in situ hybridization (FISH)

TURN AROUND TIME – 7 days

PATEINT PREPARATION –

COLLECT non diluted bone marrow aspirate or sodium heparin

SPECIMEN PREPARATION – 3-4 ml of bone marrow or peripheral blood in green top (sodium heparin) or lavender top (EDTA) tube

STORAGE/TRANSPORT TEMPERATURE – 2-8 degrees C (with cold pack) and transport within 72 hours

STABILITY – ambient: 48 hours; refrigerated: 48 hours

UNACCEPTABLE CONDITIONS – frozen or clotted specimens

MRP – 3500.00

SPECIAL INSTRUCTIONS – clinical history is mandatory

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Get Report In
7 Days
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Pre-Test Information
Clinical History is Mandatory
3,500.00
Home Collection-
Offer Price3,500.00
Total Amount₹3,500.00
*inclusive of all the taxes, fees and subject to availability

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