Answer:
1A 2A 3A 4A 5A 6A 7A 8A
(1) (2) (13) (14) (15) (16) (17) (18)
3B 4B 5B 6B 7B — 8B — 1B 2B
(3) (4) (5) (6) (7) (8) (9) (10) (11) (12)
1 1 2
2 3 4 5 6 7 8 9 10
3 11 12 13 14 15 16 17 18
4 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36
5 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54
6 55 56 57 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86
7 87 88 89 104 105 106 107 108 109 110 111 112 — 114 — — — —
6 58 59 60 61 62 63 64 65 66 67 68 69 70 71
7 90 91 92 93 94 95 96 97 98 99 100 101 102 103
Explanation:
Answer:
C
Explanation:
The mutation seen is most likely due to a frameshift mutation. A nucleotide was added or removed without replacement. This shifted the codon reading sequence by one nucleotide. Therefore the codon downstream of the mutation will code for different amino acids.
These biomoleules are found in following cellular structures.
<span>Carbohydrates- Cell wall, Golgi apparatus </span>
<span>Proteins- Plasma membrane, Endoplasmic reticulum, nucleus, cytoplasm, mitochondria, chloroplast etc. </span>
<span>Lipid- Plasma membrane, cytoplasm </span>
<span>Nucleic acid- Nucleus, chromosomes, mitochondria, chloroplast, ribosomes.</span>
Glycolysis provides a cell with a net gain of 2 ATP molecules
