MPL Exon 10 Mutation Analysis
Order Code: 4642 Get Requisition Form
Molecular test to detect mutations in Myeloproliferative Neoplasm (MPN) disorders. These disorders may include Polycythemia Vera (PV), Essential Thrombocythemia (ET), and Primary Myelofibrosis (PMF). This test detects common variants of codon 515 as well as novel variants within exon 10 and the adjacent intron boundaries.
EDTA Whole Blood (lavender top) or EDTA Bone Marrow (lavender top) or DNA (High Quality)
2-5 ml EDTA Whole Blood (lavender top) or 2-5 ml EDTA Bone Marrow (lavender top) or High Quality DNA >= 500 ng at 25 ng/ul
Minimum / Pediatric Volume
2 ml EDTA Whole Blood (lavender top) or 2 ml EDTA Bone Marrow (lavender top)
Additional Sample Information
Indicate on specimen tube and requisition whether sample/DNA is from whole blood or bone marrow.
PCR and Bi-directional DNA Sequencing
New York State Approval
Yes, visit app.dexzcodes.com