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TromboGene Kit | 2016

Genetic Study of Hereditary Thrombophilia

REF: 5039

Fully Optimised and integrated with the iPLEX® MassARRAY® system, from logo-agena

The TromboGene Kit | 2016 is a qualitative in vitro diagnostic device (IVD) for genotyping a panel of 14 genetic variants, in human genomic DNA samples, and estimating the genetic risk for hereditary thrombophilia.

Genetic Kits contain ready-to-use and fully optimised amplification and extension primer mixes, and an external control.

The genetic panel of the TromboGene Kit | 2016 comprises genetic variants that produce a deficiency in natural coagulation inhibitors or an increase in either the activity or the plasma levels of coagulation factors.

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Number of genetic variants: 14

Genes (description):
F13A1 | Coagulation factor XIII A chain
F2 | Coagulation factor II, thrombin
F5 | Coagulation factor V
FGB | Fibrinogen beta chain
GP1BA | Glycoprotein Ib platelet alpha subunit
MTHFR | Methylenetetrahydrofolate reductase (NAD(P)H)
PROCR | Protein C receptor
PROS1 | Protein S (alpha)
SERPINC1 | Serpin peptidase inhibitor, clade C (antithrombin), member 1
SERPINE1 (PAI-1) | Serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1

External control: Artificial DNA templates

Contains sufficient for: 30 tests

Shipping conditions: Room temperature

Storage: All components should be stored at -20°C upon receipt for optimum stability. Repeated freeze/thaw cycles should be avoided.


  • Customer and sample information
  • Genotyping summary table
  • Gene function and associated genetic risk
  • Phenotype/clinical profile association
  • Frequency of the genetic variant
  • Methods and analytical section
  • Trustful scientific references
  • Gene panel analysed
  • Your company information and details

European Society of Human Genetics.

Genetic reports follow all recommendations from the European Society of Human Genetics

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