Yes, sister chromatids have the same alleles within a chromosome.
Yes, sister chromatids have the same genes within them.
DNA is bundled up into a chromossome with could be one or two chromatids depending on where the cell is in its cell cycle (two chromatids give the chromossome that X look). Both chromatids are bound together by a centromere.
The chromatids are pulled apart.
I don't know weather you mean attached to the chromosome "bundle" (made of chromosomes wrapped in a tight ball) or attached to the cell (as in remaining within the cell membrain). But chromosomes come in pairs of 23. Every cell (excluding gametes) come with 46 chromosomes which come in 2 sets of 23. this cell would have not 46 but 92 if the chromosomes had replicated but not broken off into a new cell - and so would have 4 pairs of chromosomes, or 2 sets. This division happens at the start of meiosis and mitosis, however usually they then go on to divide into 2 new cells (and eventually 4 in meiosis)
The thread-like strand made of DNA is called a chromosome. Chromosomes are structures within cells that contain the genetic material needed for growth, development, and function. Humans normally have 46 chromosomes in each cell.
The replicated DNA of each individual chromosome is contained within sister chromatids, which are identical copies of a chromosome formed during DNA replication. Each chromosome consists of two sister chromatids joined together at a region called the centromere. During cell division, these sister chromatids are separated to ensure that each daughter cell receives an identical set of chromosomes.
Yes, sister chromatids have the same genes within them.
The two coiled up strands of DNA within a chromosome are called chromatids. During cell division, chromatids separate and are distributed to daughter cells.
A chromosome unit refers to a single chromosome, which is a long strand of DNA containing genetic information. In humans, a chromosome unit consists of two sister chromatids joined together at a centromere. Chromosomes are located within the nucleus of cells and play a crucial role in storing and transmitting genetic information during cell division.
DNA is bundled up into a chromossome with could be one or two chromatids depending on where the cell is in its cell cycle (two chromatids give the chromossome that X look). Both chromatids are bound together by a centromere.
The chromatids are pulled apart.
In order to fit within a cell, DNA becomes more compact by wrapping tightly around associated proteins. Chromatids are duplicate halves of a chromosome.
Chromosome inversions are caused by breaks in the chromosome followed by rejoining in an inverted orientation. This can happen due to errors during cell division or exposure to mutagens. Inversions can also be inherited from parents.
Homologous pairs of chromosomes are held together by a structure called the synaptonemal complex during meiosis. This complex facilitates the pairing and alignment of homologous chromosomes, allowing for genetic recombination or crossing over. Additionally, cohesion proteins help maintain the connection between sister chromatids within each homologous chromosome.
I don't know weather you mean attached to the chromosome "bundle" (made of chromosomes wrapped in a tight ball) or attached to the cell (as in remaining within the cell membrain). But chromosomes come in pairs of 23. Every cell (excluding gametes) come with 46 chromosomes which come in 2 sets of 23. this cell would have not 46 but 92 if the chromosomes had replicated but not broken off into a new cell - and so would have 4 pairs of chromosomes, or 2 sets. This division happens at the start of meiosis and mitosis, however usually they then go on to divide into 2 new cells (and eventually 4 in meiosis)
The thread-like strand made of DNA is called a chromosome. Chromosomes are structures within cells that contain the genetic material needed for growth, development, and function. Humans normally have 46 chromosomes in each cell.
A chromosome is made up of DNA, protein, and RNA. The DNA contains the genetic information necessary for an organism's growth and development, while the proteins help the DNA stay organized and compacted within the chromosome structure. RNA is involved in various functions related to gene expression and regulation.