QF PCR and Karyotyping Test
Welcome to DNA Labs UAE, a leading genetic lab offering QF PCR and Karyotyping Test for comprehensive analysis of genetic and chromosomal characteristics. Our test provides valuable information for diagnostic and research purposes.
Test Details
QF PCR (Quantitative Fluorescent Polymerase Chain Reaction) is a molecular technique used to quantify the amount of a specific DNA sequence in a sample. It involves amplifying the target DNA sequence using PCR and then measuring the fluorescence intensity to determine the quantity of the target sequence.
Karyotyping, on the other hand, is a cytogenetic technique used to visualize and analyze the chromosomes of an individual. It involves staining the chromosomes and arranging them in a specific order to observe any structural abnormalities or numerical changes in the genome.
When combining QF PCR with karyotyping, it is possible to analyze specific DNA markers in the context of the overall chromosomal structure. This can be particularly useful in identifying genetic abnormalities or mutations associated with certain diseases or conditions.
For example, if a specific DNA marker is suspected to be involved in a genetic disorder, QF PCR can be used to quantify the presence or absence of the marker, while karyotyping can provide information on the overall chromosomal structure and identify any chromosomal abnormalities that may be associated with the disorder.
Overall, the combination of QF PCR and karyotyping allows for a more comprehensive analysis of the genetic and chromosomal characteristics of an individual, providing valuable information for diagnostic and research purposes.
Test Components
- Sterile container/ Sterile Normal Saline Container/ EDTA & Sodium Heparin Vacutainer (2-3 ml. each)
Price
AED 2100.0
Sample Condition
Amniotic fluid/ Chorionic villi/ Cord Blood
Report Delivery
1-2 days/12-15 days
Method
Cell culture + Sanger Sequencing
Test Type
Genetics
Doctor
Gynecologist
Test Department
Pre Test Information
QF PCR any one marker]+ Karyotyping can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
| Test Name | QF PCR any one markerand Karyotyping Test |
|---|---|
| Components | Sterile container/ Sterile Normal Saline Container/ EDTA & Sodium Heparin Vacutainer (2-3 ml. each) |
| Price | 2100.0 AED |
| Sample Condition | Amniotic fluid\/ Chorionic villi\/ Cord Blood |
| Report Delivery | 1-2 days/12-15 days |
| Method | Cell culture + Sanger Sequencing |
| Test type | Genetics |
| Doctor | Gynecologist |
| Test Department: | |
| Pre Test Information | QF PCR any one marker]+ Karyotyping can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
| Test Details |
QF PCR (Quantitative Fluorescent Polymerase Chain Reaction) is a molecular technique used to quantify the amount of a specific DNA sequence in a sample. It involves amplifying the target DNA sequence using PCR and then measuring the fluorescence intensity to determine the quantity of the target sequence. Karyotyping, on the other hand, is a cytogenetic technique used to visualize and analyze the chromosomes of an individual. It involves staining the chromosomes and arranging them in a specific order to observe any structural abnormalities or numerical changes in the genome. When combining QF PCR with karyotyping, it is possible to analyze specific DNA markers in the context of the overall chromosomal structure. This can be particularly useful in identifying genetic abnormalities or mutations associated with certain diseases or conditions. For example, if a specific DNA marker is suspected to be involved in a genetic disorder, QF PCR can be used to quantify the presence or absence of the marker, while karyotyping can provide information on the overall chromosomal structure and identify any chromosomal abnormalities that may be associated with the disorder. Overall, the combination of QF PCR and karyotyping allows for a more comprehensive analysis of the genetic and chromosomal characteristics of an individual, providing valuable information for diagnostic and research purposes. |
