suppose P is a dominant allele for a flower color and p is a recessive one.
The expected ratio of genotypes among the F1 offspring is 1 Pp : 1 pp.
The white pea bloom was "masked" in the F1 generation, which caused all of the flowers to be purple.
The "masked" genes from the F1 generation were permitted to mate, but they were only allowed to pair once, leaving the other three times to appear with purple flowers, resulting in a 3:1 ratio of purple to white blooms in generation F2.
He paired a homozygous dominant flower with a homozygous recessive flower in his initial attempt. As a result, all of the F1 generation's progeny were heterozygous, making them all purple.
Two heterozygous, one homozygous recessive, one homozygous dominant, and the progeny of the F1 generation were crossed with another heterozygous plant.
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Answer:
C. Running on track
Explanation:
kinetic energy depends upon velocity
(or speed of object )
hence , more the velocity ,
more kinetic energy it have.
so during running , we are in highest velocity
<h3>hope it helps</h3>
Mixtures can be separated my physical means is true
mixtures are made up of more than one component is true
all else is false I believe
Answer:The correct answer is letter A.
Explanation: he is right
Your teacher gives you an unknown protist to classify that is currently inactive. The protist appears to have long lash-like
appendages protruding from its cell surface. Which kind of locomotion can we expect from this protist? (1 point)
The appendages of this protist will move in a dragging motion that actively pulls the protist forward.
O The appendages of this protist will move in a sweeping motion like oars to actively propel the protist forward.
The appendages of this protist will move back and forth like a wagging tail to actively propel the protist
forward
O The appendages of this protist are not functional, and the protist moves passively via environmental forces.
Answer:
CF is caused by a mutation in the gene cystic fibrosis transmembrane conductance regulator (CFTR). The most common mutation, ΔF508, is a deletion (Δ signifying deletion) of three nucleotides that results in a loss of the amino acid phenylalanine (F) at the 508th position on the protein.
