Hi There!
Tell me a little about prokaryotic and eukaryotes.
What do these types of cells have in common?
How are they different?
2 very common similarities between the types of cells is that they both have a certain type of structure and all cells have a plasma membrane, DNA, ribosome, etc. They are different in a way that eukaryotes have a "membrane-bound organelle" which usualy includes it having a nucleus. Whats cool is that eukaryotes can be multicellular or singled celled> For Example, plants, insects, and fungi. Prokaryotes don't have a nucleus or organelle (membrane bound).
Hope This Helps :)
Answer:
Solar phenomena are the natural phenomena occurring within the outer atmosphere of the Sun. These phenomena take many forms, including solar wind, radio wave flux, solar flares, coronal mass ejections, coronal heating and sunspots.
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<span>The correct answer for the question is Non-disjunction. Non-disjunction occurs in cell division when chromosomes do not divide properly. It can occur during mitosis, meiosis I and meiosis II. In mitosis it occurs when sister chromatids fails to separate in Anaphase. The result is that one cell receives both chromatids, while the other receives neither. Each daughter cell then has an abnormal number of chromosomes when mitosis is complete; one cell has an extra chromosome, while the other is missing one. In anaphase of meiosis I, it happens when a pair of homologous chromosomes does not separate. In meiosis II, it happens when a pair of sister chromatids fails to separate properly during anaphase of meiosis II, one daughter cell will have an extra chromosome and one daughter cell will be missing a chromosome.</span>
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.
