Microscopes coupled with techniques used to separate them from inside the cell.
They have homologous chromosomes
Two sets of chromosomes, one from each parent, resulting in pairs of homologous chromosomes. This genetic configuration allows for genetic diversity through recombination during meiosis.
Body cells typically have a diploid number of chromosomes, meaning they have two sets of chromosomes. Sex cells, or gametes, have a haploid number of chromosomes, meaning they have one set of chromosomes. This allows for the correct number of chromosomes to be restored upon fertilization.
Pairs of chromosomes in a karyotype are significant because they represent one set of chromosomes from each parent. Having pairs of chromosomes ensures genetic diversity and allows for the inheritance of traits from both parents. This pairing is necessary for proper cell division and genetic stability in an individual.
In oogonium, the number of chromosomes is diploid, meaning they have the full set of chromosomes (46 in humans). This allows for meiotic divisions to produce haploid egg cells with half the number of chromosomes.
Metaphase Metaphase
During telophase, the process of chromatin condensation occurs, which allows chromosomes to uncoil and facilitate gene expression.
Giemsa is the most common stain used to see banding patterns in chromosomes
centromere
Starting with a diploid number of chromosomes (two of each chromosome) and a single cell, the process of meiosis will result in four cells with a haploid number of chromosomes (one of each chromosome). This allows genetic recombination through the combining of gametes from different somatic organisms.
Gametes have an odd number of chromosomes due to the process of meiosis, where the number of chromosomes is halved. This allows for the fusion of gametes during fertilization to produce offspring with the correct number of chromosomes.
2n= 24 therefore one set consists of 12 chromosomes.