In complementary base pairing, the G pairs with C, and A pairs with T. Given that this be the rule, the complementary nucleotides for your sequence would be as follows: CGATTAACGTAGGCA.
With regards to proofreading, mutations in cell division occur once in around every 100,000 base pairs. If this happens, the enzyme that pairs the nucleotides to form DNA, called DNA polymerase, detects the error and moves back along the strand, it then cuts the incorrect nucleotide and replaces it with the correct one, fixing the error and continuing with the DNA synthesis.
This process corrects the majority of errors in DNA synthesis, but some errors can still be missed by the DNA polymerase, this is then rectified by a protein complex which binds to the incorrect pairing until anther complex, comes along and cuts that particular section of DNA out, which is then replaced by a new section of correct nucleotides synthesized by the polymerase enzyme, the two sections at either end that were cut is then sealed by ligase, an enzyme which essentially "glues" the DNA stands back together.
My apologies for the long answer, I hope I answered your question and that you understand it well enough.
54954 gmfn 45443 rfe546654
The term "lipid" does not specify a particular chemical structure. Whereas one can write a general formula for an amino acid, nucleic acid, or protein, lipids are much more chemically diverse. Compounds are categorized as lipids based on their greater solubility in organic solvents than in water.
The right answer is metaphase II.
The process is performed in two nuclear and cytoplasmic divisions, called first and second meiotic division or simply meiosis I and meiosis II. Both include prophase, metaphase, anaphase, and telophase. First division prophase is long and consists of 5 stages: leptotene, zygotene, pachytene, diplotene, and diakinesis. It is at this point that genetic recombination takes place at the level of chiasmus.
During meiosis I, the members of each homologous pair of chromosomes are paired during prophase, forming bivalents. During this phase, a protein structure, called synaptonemal complex form, allows recombination between homologous chromosomes. Subsequently, a large condensation of the bivalent chromosomes occurs and go to the metaphase plate during the first metaphase, resulting in the migration of n chromosomes to each of the poles during the first anaphase. This reduction division is responsible for maintaining the number of chromosomes characteristic of each species.
In meiosis II, as in mitosis, the sister chromatids comprising each chromosome are separated and distributed between the nuclei of the daughter cells. Between these two successive steps, there is no DNA replication. The maturation of the daughter cells will result in the gametes.
