PANAMutyper™ c-Met (exon 14 skipping)
Ref. PNAR-7101PANAMutyper™ c-Met (exon 14 skipping) is an in vitro diagnostic test kit to detect gene alteration in c-Met oncogene. The kit is developed to be used by the trained laboratory professionals, within the fully equipped laboratory environment, using the RNA derived from formalin-fixed paraffin-embedded (FFPE) tissue of…
About the Product
PANAMutyper™ c-Met (exon 14 skipping) is an in vitro diagnostic test kit to detect gene alteration in c-Met oncogene. The kit is developed to be used by the trained laboratory professionals, within the fully equipped laboratory environment, using the RNA derived from formalin-fixed paraffin-embedded (FFPE) tissue of non-small cell lung cancer (NSCLC) patients.
PANAMutyper™ c-Met (exon 14 skipping) is intended as an aid for NSCLC patients who would be sensitive for receiving c-Met inhibitor therapy.
Technical Characteristics
| C-MET Mutation 1 |
|
|---|---|
| Procedure | DNA ExtractionPCR SetupReal-time PCRResult Analysis |
Key Features
- Detect exon 14 skipping of c-Met mutation using 1 reaction tubes
- One-step reverse-transcription qPCR
- High sensitivity and specificity
- Convenient testing with master mix format
- Automated result analysis software
Technical Information
No technical information available for this product.
Compatibility
Compatible sample type: Formalin-fixed paraffin-embedded (FFPE) tissue
Compatible Real-Time PCR machine:
- CFX96 (Bio-Rad)
- QuantStudio® 5
Packaging
No packaging information available for this product.