Answer:
option b i think so i think its correct
Answer:
Tropomyosin
Explanation:
The calcium binding to troponin and induces the muscle contraction. The active binding site gets exposed due to the calcium binding.
The calcium ions then attaches with troponin molecule. This changes the shape of troponin and removes the tropomyosin protein from the binding site. No ATP is available during this process.
Thus, the correct answer is option (d).
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1. The main aim of the Human Genome Project was to determine the DNA Sequence of every human gene.
2. Variation in skin colour is an example of polygenic inheritance
This Human Karyotype is unusual because it has an extra chromosome at chromosome 21.
Klinefelters syndrome is shown in the second figure
Explanation:
1. The Human Genome Project's main goal was to sequence all the 30,000 genes and 3 million base pairs in their makeup for the early detection of diseases, gene therapy and molecular level studies.
2. Human skin colour is determined by the pigment melanin. The Dominant allele is responsible for dark colours as it produces more melanin. The melanocortin 1 receptor (MC1R) gene and Tyrosinase enzyme codes for the human skin colour. Polygenic inheritance are the traits which are controlled by one or more genes.
<u>figures:</u>
<u>The extra chro</u>mosome at the 21st chromosome pairs is called trisomy 21 or Down's Syndrome. It is due to the abnormal cell division/meiosis resulting in an extra X chromosome. This leads to thechanges the in physical development of the individual.
Klinefelter's Syndrome: There are 47 chromosomes and 2 or more X chromosomes in this syndrome of males. The resulting male suffering from Klinefelter would be sterile and have poorly developed testicles.
a subatomic particle of about the same mass as a proton but without an electric charge, present in all atomic nuclei except those of ordinary hydrogen.
