bruuuh isnt this the american server
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
The answer would be:
Cilium
<u>Here is more about the structures of prokaryotic cells:</u>
Axial filament is a bundle of flagella that are wrapped around the cell's body.
Flagellum is what the prokaryotic cell has that is whip-like in structure. It helps with the motility of the cell.
Pilus is a hair-like structure that are found on the surface of prokaryotic cells. They help the cell attach itself to surfaces.
Peritrichous flagella are several flagella that can be found all over some prokaryotic cells.
I have a question are you asking what are the molecules of a shark or something
Glycolysis does not need any oxygen to function
