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VWF D1472H Ristocetin-Binding Polymorphism

Order Code: 1301

Also Known as

Von Willebrand Disease, VWF

Disease State

Test Information

This assay is designed for detection of the D1472H polymorphism within the VWF gene.

Sample Requirements

Amniotic Fluid, Buccal Swabs, Cultured Amniocytes, CVS, DNA, EDTA Bone Marrow, EDTA Whole Blood

Additional Sample Requirements

Sample should be less than 7 days old when received in the laboratory.

Shipping Information

Room Temperature

Requested Volume

3-5 mL EDTA Whole Blood or Bone Marrow (lavender top), 3-4 Buccal Swabs, 1 ug DNA at 50 ng/uL, 7-15 mL Amniotic Fluid, 5-10 mg CVS, 2-T25 flasks cultured amniocytes or CVS (2x10^6 minimum)

Minimum/Pediatric Volume

1 ml EDTA whole blood

CPT Codes

81479

Method

PCR and Bi-directional DNA Sequencing

Turnaround Time

7-10 days

DEX Z-Code™

Yes, visit app.dexzcodes.com

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