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Cell Line Name Well Lot Number Provider Banked By Thaw and Culture Recommendations Culture PlatformThaw and Culture DetailsUCSD067i191 WB64878 University of California, San Diego Dr. Kelly Fraser
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How to fill out karyotype by g-banding

01
Obtain a sample of the patient's cells, typically from a blood sample.
02
Culture the cells in a lab dish to stimulate cell division.
03
Add a chemical that stops cell division at a specific phase to capture the chromosomes in their most condensed state.
04
Stain the chromosomes with a Giemsa stain to create a pattern of light and dark bands.
05
Examine the stained chromosomes under a microscope and photograph them to create a karyotype.
06
Arrange the chromosomes in pairs based on their size, banding patterns, and centromere location.
07
Analyze the karyotype for any abnormalities or chromosomal rearrangements.

Who needs karyotype by g-banding?

01
Patients with suspected genetic disorders or chromosomal abnormalities
02
Individuals undergoing fertility treatments
03
Patients with certain types of cancer to understand the genetic basis of the disease
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Karyotype by g-banding is a laboratory technique used to visualize the number and structure of chromosomes in a cell. It involves staining chromosomes with a dye, usually Giemsa stain, which produces a distinct pattern of bands that can be used to identify and diagnose genetic abnormalities.
Typically, medical professionals, such as geneticists and cytogeneticists, are required to file karyotype by g-banding as part of genetic testing procedures, especially in cases of suspected genetic disorders or chromosomal abnormalities.
Filling out a karyotype by g-banding involves collecting blood or tissue samples, preparing the samples for chromosome analysis, performing the G-banding technique, and then documenting the results in a standardized format that includes chromosome count, abnormalities, and other relevant genetic information.
The purpose of karyotype by g-banding is to identify chromosomal abnormalities that may be associated with genetic disorders, guide clinical decision-making, and provide information for prenatal testing, cancer diagnosis, and infertility investigations.
The information that must be reported on karyotype by g-banding includes the total number of chromosomes, the sex chromosomes, any structural abnormalities, and a description of any additional findings that may be clinically relevant.
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