Humans have 23 pairs of chromosomes: 22 autosomes and a
pair of sex chromosomes. The method by which the chromosomes are identified and counted is called karyotyping. Human cells are placed in a solution that stimulates them to divide by mitosis but the drug colchicines is added to the solution , which prevents the formation of spindle microtubules. The chromosomes remain in metaphase. They are fixed, stained and mounted so that they can be photographed.
Apparatus:
Scissors, glue, paper
Method:
1. Chromosomes were cut out from diagram and arranged in
pairs and groups as seen in previous diagram.
2. Cut chromosomes were glued to a fresh sheet of paper.
Discussion:
A karyotype is the number and appearance of chromosomes
in the nucleus of a eukaryotic cell. The total number of chromosomes present from arrangement is forty-six (46).The individual is observed to be a female as there is the presence of the sex chromosome X in the karyotype. With no Y chromosome present and only an X the individual would have to be female as XX: female and XY: male. A numerical disorder of the chromosomes is apparent as some chromosomes are missing and some are in excess showcasing the condition to be aneuploidy and the individual to be diagnosed with Turner Syndrome due to presence of single X chromosome.
Conclusion:
The karyotype investigated presented the aneuploidy
condition of chromosomes, showed that the person was female and has Turner Syndrome.