Targeted Mutation Analysis 1 Mutation Test Cost AED 1800.0
Introduction
Targeted mutation analysis is a technique used in molecular biology to identify and analyze specific mutations in a gene or genome. It involves the design and use of specific primers or probes that can specifically detect and amplify the region of interest containing the mutation.
Test Details
The targeted mutation analysis test offered by DNA Labs UAE is designed to detect and analyze 1 specific mutation. The test uses the Sanger sequencing method, which is a widely used technique in genetics. The test can be performed using various sample types, including peripheral blood, plasma, serum, amniotic fluid, cord blood, and chorionic villi.
Components
- EDTA Vacutainer (2ml) or Sterile Container
Price
The cost of the targeted mutation analysis 1 mutation test is AED 1800.0.
Sample Condition
The test can be performed on peripheral blood, plasma, serum, amniotic fluid, cord blood, or chorionic villi samples.
Report Delivery
The test report will be delivered within 10-15 days.
Test Type
The targeted mutation analysis 1 mutation test falls under the genetics category.
Doctor
This test can be requested by a gynecologist.
Test Department
This test is conducted in the genetics department of DNA Labs UAE.
Pre Test Information
Targeted mutation analysis (1 mutation) can be done with a doctor’s prescription. However, prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Advantages of Targeted Mutation Analysis
Targeted mutation analysis offers several advantages compared to whole-genome sequencing:
- Precise and efficient analysis of specific mutations
- Saves time and resources
- Allows for the identification of disease-causing mutations
- Enables the study of the effects of specific mutations on gene function
Conclusion
The targeted mutation analysis 1 mutation test offered by DNA Labs UAE is a valuable tool in molecular biology research and clinical settings. It allows for the precise and efficient analysis of specific mutations, saving time and resources compared to whole-genome sequencing. The test can be performed on various sample types and is conducted in the genetics department. With a cost of AED 1800.0, this test provides valuable insights into the presence and functional consequences of specific mutations.
Test Name | Targeted mutation Analysis 1 mutation Test |
---|---|
Components | EDTA Vacutainer (2ml)/ Sterile Container |
Price | 1800.0 AED |
Sample Condition | Peripheral blood\/ Plasma\/ Serum\/Amniotic fluid \/ Cord Blood\/Chorionic villi |
Report Delivery | 10-15 days |
Method | Sanger Sequencing |
Test type | Genetics |
Doctor | Gynecologist |
Test Department: | |
Pre Test Information | Targeted mutation Analysis (1 mutation) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details |
Targeted mutation analysis is a technique used in molecular biology to identify and analyze specific mutations in a gene or genome. It involves the design and use of specific primers or probes that can specifically detect and amplify the region of interest containing the mutation. In the case of 1 mutation, the targeted mutation analysis would involve designing primers or probes that can specifically amplify the region of the gene where the mutation is located. This can be done using techniques such as polymerase chain reaction (PCR) or DNA sequencing. Once the region of interest is amplified or sequenced, the presence or absence of the mutation can be determined by comparing the obtained sequence with the reference or wild-type sequence. If the mutation is present, further analysis can be done to determine the functional consequences of the mutation, such as its effect on protein structure or function. Targeted mutation analysis is commonly used in research and clinical settings to identify disease-causing mutations or to study the effects of specific mutations on gene function. It allows for precise and efficient analysis of specific mutations, saving time and resources compared to whole-genome sequencing. |