FISH for X and Y Test
Test Name: FISH for X and Y Test
Components: Fluorescent probes
Price: 1200.0 AED
Sample Condition: N/A
Report Delivery: 1 week
Method: FISH (Fluorescence In Situ Hybridization)
Test Type: Gynecology
Doctor: Gynecologist
Test Department: Cytogenetics
Pre Test Information:
FISH stands for Fluorescence In Situ Hybridization, a technique used in molecular biology to visualize and locate specific DNA sequences on chromosomes. It involves the use of fluorescent probes that bind to complementary DNA sequences, allowing researchers to identify and track specific genes or chromosomal abnormalities.
In the context of “FISH for X and Y,” it refers to the use of FISH to determine the presence or absence of the X and Y chromosomes in a biological sample. This is commonly done in prenatal testing to identify the sex of a fetus or in genetic testing to diagnose disorders related to sex chromosome abnormalities.
By using specific probes that target DNA sequences unique to the X and Y chromosomes, FISH can determine whether an individual has two X chromosomes (XX, female) or one X and one Y chromosome (XY, male). The fluorescent signals emitted by the probes allow for visualization and identification of the chromosomes under a microscope.
Overall, FISH for X and Y is a valuable tool in genetic analysis, providing important information about an individual’s sex and helping diagnose certain genetic disorders.
Test Name | FISH for X and Y Test |
---|---|
Components | |
Price | 1200.0 AED |
Sample Condition | |
Report Delivery | 1 week |
Method | FISH |
Test type | Gynecology |
Doctor | Gynecologist |
Test Department: | Cytogenetics |
Pre Test Information | |
Test Details | FISH stands for Fluorescence In Situ Hybridization, a technique used in molecular biology to visualize and locate specific DNA sequences on chromosomes. It involves the use of fluorescent probes that bind to complementary DNA sequences, allowing researchers to identify and track specific genes or chromosomal abnormalities. In the context of “FISH for X and Y,” it refers to the use of FISH to determine the presence or absence of the X and Y chromosomes in a biological sample. This is commonly done in prenatal testing to identify the sex of a fetus or in genetic testing to diagnose disorders related to sex chromosome abnormalities. By using specific probes that target DNA sequences unique to the X and Y chromosomes, FISH can determine whether an individual has two X chromosomes (XX, female) or one X and one Y chromosome (XY, male). The fluorescent signals emitted by the probes allow for visualization and identification of the chromosomes under a microscope. Overall, FISH for X and Y is a valuable tool in genetic analysis, providing important information about an individual’s sex and helping diagnose certain genetic disorders. |