Microarray 315K AFCVSCBPOCPB Test
Welcome to DNA Labs UAE, a leading genetic lab offering the Microarray 315K AFCVSCBPOCPB Test. In this blog, we will discuss the test cost, symptoms diagnosis, and other important details related to this test.
Test Details
The Microarray 315K AFCVSCBPOCPB Test refers to a type of microarray technology that is capable of analyzing 315,000 different DNA sequences. The acronym AFCVSCBPOCPB stands for Amniotic Fluid, Chorionic Villus Sampling, Cord Blood, Products of Conception, and Peripheral Blood, which are different types of samples that can be analyzed using this microarray technology.
Microarrays are tools used in genetic research and diagnostics to analyze the expression levels of thousands of genes simultaneously. They consist of small glass or silicon chips that contain thousands of DNA probes, which are short sequences of DNA that can bind to specific target sequences. By hybridizing the DNA samples to the microarray, researchers can determine which genes are expressed in a particular sample and at what levels.
The Microarray 315K AFCVSCBPOCPB Test is specifically designed to analyze samples obtained from amniotic fluid, chorionic villus sampling, cord blood, products of conception, and peripheral blood. These samples are commonly used in prenatal testing and genetic research to detect chromosomal abnormalities, genetic disorders, and other genetic variations.
By using this microarray technology, researchers and clinicians can obtain a comprehensive view of the genetic information present in the samples, allowing for the identification of potential genetic abnormalities or variations. This information can be crucial in making accurate diagnoses, providing personalized treatment options, and offering genetic counseling to patients and families.
Test Cost
The cost of the Microarray 315K AFCVSCBPOCPB Test is AED 3300.0.
Symptoms Diagnosis
The Microarray 315K AFCVSCBPOCPB Test can help in diagnosing various genetic conditions, chromosomal abnormalities, and genetic disorders. It is commonly used in prenatal testing to detect any potential issues in the developing fetus. By analyzing the genetic information present in the samples, clinicians can identify symptoms and provide an accurate diagnosis.
Sample Condition
The Microarray 315K AFCVSCBPOCPB Test can be performed using samples of amniotic fluid, chorionic villi, products of conception, cord blood, and peripheral blood. These samples need to be collected and stored in sterile containers or EDTA vacutainers. It is important to ensure the samples are in proper condition for accurate testing.
Report Delivery
The report for the Microarray 315K AFCVSCBPOCPB Test is typically delivered within 7-9 days. This allows for thorough analysis and interpretation of the genetic information obtained from the samples.
Method
The Microarray 315K AFCVSCBPOCPB Test uses microarray technology from Affymetrix. This technology allows for the simultaneous analysis of thousands of DNA sequences, providing a comprehensive view of the genetic information present in the samples.
Test Type
The Microarray 315K AFCVSCBPOCPB Test falls under the category of genetics testing. It is specifically designed to analyze genetic information and identify potential abnormalities or variations.
Doctor
The Microarray 315K AFCVSCBPOCPB Test is typically recommended by gynecologists. They have the expertise and knowledge to understand the importance of genetic testing, especially in prenatal care and diagnosing genetic conditions.
Test Department
The Microarray 315K AFCVSCBPOCPB Test is conducted in the genetics test department of DNA Labs UAE. Our specialized team of genetic experts ensures accurate testing and interpretation of the results.
Pre Test Information
The Microarray 315K AFCVSCBPOCPB Test requires a doctor’s prescription. However, it is not applicable for surgery and pregnancy cases or individuals planning to travel abroad. This ensures that the test is conducted under appropriate circumstances and with proper medical guidance.
At DNA Labs UAE, we are committed to providing reliable and accurate genetic testing services. The Microarray 315K AFCVSCBPOCPB Test is one of the many tests we offer to help individuals and healthcare professionals in diagnosing genetic conditions and making informed decisions about treatment and care.
Test Name | Microarray 315K AFCVSCBPOCPB Test |
---|---|
Components | Sterile Container/ Sterile Normal Saline Container/EDTA vacutainer (3ml each) |
Price | 3300.0 AED |
Sample Condition | Amniotic fluid\/ Chorionic villi\/Products of Conception\/Cord blood\/Peripheral blood |
Report Delivery | 7-9 days |
Method | Microarray Affymetrix] |
Test type | Genetics |
Doctor | Gynecologist |
Test Department: | |
Pre Test Information | Microarray 315K (AF/CVS/CB/POC/PB) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details |
Microarray 315K (AF/CVS/CB/POC/PB) refers to a type of microarray technology that is capable of analyzing 315,000 different DNA sequences. The acronym AF/CVS/CB/POC/PB stands for Amniotic Fluid, Chorionic Villus Sampling, Cord Blood, Products of Conception, and Peripheral Blood, which are different types of samples that can be analyzed using this microarray technology. Microarrays are tools used in genetic research and diagnostics to analyze the expression levels of thousands of genes simultaneously. They consist of small glass or silicon chips that contain thousands of DNA probes, which are short sequences of DNA that can bind to specific target sequences. By hybridizing the DNA samples to the microarray, researchers can determine which genes are expressed in a particular sample and at what levels. The Microarray 315K (AF/CVS/CB/POC/PB) is specifically designed to analyze samples obtained from amniotic fluid, chorionic villus sampling, cord blood, products of conception, and peripheral blood. These samples are commonly used in prenatal testing and genetic research to detect chromosomal abnormalities, genetic disorders, and other genetic variations. By using this microarray technology, researchers and clinicians can obtain a comprehensive view of the genetic information present in the samples, allowing for the identification of potential genetic abnormalities or variations. This information can be crucial in making accurate diagnoses, providing personalized treatment options, and offering genetic counseling to patients and families. |