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yKpoI14uk [10]
3 years ago
7

Mendel crossed two plants that were heterozygous for purple flower color. Which genotypes could he have used to represent the cr

oss?
Biology
2 answers:
Dennis_Churaev [7]3 years ago
6 0

Answer:

I think its B

Explanation:

Srry if wrong

ICE Princess25 [194]3 years ago
3 0
The answer is two Pp genotypes.

If we imagine that plant has two alleles for the trait and if P represents dominant allele, and p represents recessive allele, then genotypes are:
PP - dominant homozygous, which contains both dominant alleles
pp - recessive homozygous, <span>which contains both recessive alleles</span>
Pp - heterozygous, which contains both dominant and recessive alleles
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2 years ago
Place the following events of muscle excitation in the correct order.
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An motion potential in the presynaptic cell activates calcium channels. Ca+ triggers the discharge of Acetylcholine through exocytosis. Ach binds its receptors in the postsynaptic membrane, opening Na+ channels. The Order is 4, 3, 5, 1, 2.

The principal frightened system generates an motion potential that travels to the goal activating the calcium channels ⇒ event (4)

Calcium triggers vesicles fusion to the presynaptic membrane. By exocytosis, vesicles release the neurotransmitter -Acetylcholine- into the synaptic space ⇒ event (3)

Once there, Ach binds to its receptors on the postsynaptic membrane of the skeletal muscle fiber, causing ion channels to open ⇒ event (5)

Positively charged sodium ions move the membrane to get into the muscle fiber (sarcoplasm) and potassium leaves the cell ⇒ event (1)

The distinction in charges, resulting from these ions' transport, positively charges the fiber membrane. The postsynaptic cell depolarizes ⇒ Event (2)

The motion potential enters the t-tubules depolarizing the internal part of the muscle fiber. Contraction initiates while the motion potential depolarizes the internal part of the muscle fiber. Calcium channels spark off in the T tubules membrane, releasing calcium into the sarcolemma.

At this point, the muscle is at rest, and the tropomyosin is inhibiting the appeal strengths between myosin and actin filaments. Tropomyosin is obstructing binding sites for myosin on the skinny filament.

When calcium enters the sarcolemma, it binds to troponin C, and troponin T alters the tropomyosin role through shifting it and unblocking the binding sites.

Myosin heads be a part of the uncovered actin-binding points forming move-bridges, and whilst doing so, ATP turns into ADP and inorganic phosphate, that's released.

Myofilaments slide impulsed through chemical energy accumulated in myosin heads, generating a strength stroke. The strength stroke initiates while the myosin move-bridge binds to actin. As they slide, ADP molecules are released. A new ATP hyperlinks to myosin heads and breaks the bindings to the actin filament.

Then ATP splits into ADP and phosphate, and the energy produced is gathered in the myosin heads, which begins offevolved a new binding cycle to actin.

Finally, Z-bands are pulled towards every other, and the sarcomere and the I-band get shorter, generating muscle fiber contraction.

According to those steps, the appropriate order of activities is 4, 3, 5, 1, 2.

To learn more about Acetylcholine, click here:

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