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If the chromosome is a submetacentric chromosome (One arm big and the other arm small) then the centromere divides each chromosome into two regions: the smaller one, which is the p region, and the bigger one, the q region. The sister chromatids will be distributed to each daughter cell at the end of the cell division.
This is an accepted version of this page This is the latest accepted revision, reviewed on 23 January 2025. DNA molecule containing genetic material of a cell This article is about the DNA molecule. For the genetic algorithm, see Chromosome (genetic algorithm). Chromosome (10 7 - 10 10 bp) DNA Gene (10 3 - 10 6 bp) Function A chromosome and its packaged long strand of DNA unraveled. The DNA's ...
G-banding, G banding or Giemsa banding is a technique used in cytogenetics to produce a visible karyotype by staining condensed chromosomes. It is the most common chromosome banding method. [1] It is useful for identifying genetic diseases (mainly chromosomal abnormalities) through the photographic representation of the entire chromosome ...
The 23 human chromosome territories during prometaphase in fibroblast cells. In cell biology, chromosome territories are regions of the nucleus preferentially occupied by particular chromosomes. Interphase chromosomes are long DNA strands that are extensively folded, and are often described as appearing like a bowl of spaghetti.
They are observed in acrocentric chromosomes. In addition to the centromere, one or more secondary constrictions can be observed in some chromosomes at metaphase. In humans they are usually associated with the short arm of an acrocentric chromosome, [1] such as in the chromosomes 13, 14, 15, 21, & 22.
Chromosome 5 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 5 spans about 182 million base pairs (the building blocks of DNA) and represents almost 6% of the total DNA in cells. Chromosome 5 is the 5th largest human chromosome, yet has one of the lowest gene densities.
The related phenomena can be caused by unusual activity of the SRY in XX male syndrome, usually when it's translocated onto the X-chromosome and its activity is only activated in some cells. [26] Mutation or deletion of SOX9 could cause an XY fetus to be female because SOX9 is a critical effector gene that works because of the SRY gene to ...
Metaphase chromosomes make the classical picture of chromosomes . For classical cytogenetic analyses, cells are grown in short term culture and arrested in metaphase using mitotic inhibitor . Further they are used for slide preparation and banding ( staining ) of chromosomes to be visualised under microscope to study structure and number of ...