PNAClamp™ JAK2 Kit 25 test/kit

Panagene
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JAK2 V617F mutation is found in patients with blood related disease such as Polycythemia Vera, Essential Thrombocythemia and Myelofibrosis. Ruxolitinib is effective as a JAK Inhibitor, so that it is a prognostic factor to determine drug response.
JAK2 V617F mutation detection makes easy to classify patients with MPD (Myeloproliferative Disease) as three levels of diagnostic certainty (possible, probable and definite) and to determine which signal transduction therapy is suitable for each patients. In addition, testing for JAK2 V617F mutation has been recommended as clinical tests by WHO(World Health Organization).

EGP 49,875.00

Available on backorder

JAK2 V617F mutation can be detected by PNAClamp™ JAK2 Mutation Detection Kit. 


 Mutations

Size 

 Exon 14

25 tests 

 V617F (1849G>T)

FEATURES

  • 01High sensitivity and specificity even with small amount of DNA (1% LOD with 10 ng wild/mutant type mixed DNA)
  • 02Real-Time PCR based ready-to-use kit
  • 03Short running time (within 3 hours)

PROCEDURE

  1. Sample preparation
  2. Extraction of DNA
  3. Real-time PCR
  4. Result Analysis

COMPATIBLE SAMPE TYPE

– Blood

COMPATIBLE REAL-TIME PCR MACHINE

  1. CFX96(Bio-Rad)
  2. ABI7500 (Thermo Fisher Scientific)
  3. Rotor-Gene Q (Qiagen)
  4. LightCycler 480II (Roche)
  5. ABI7900HT (Thermo Fisher Scientific)
SKU: PNAC-6001 Category: Tags: , ,

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