It is assumed that organisms with similar anatomical characteristics have evolved relatively recently and have a common ancestor.
<h3>How does comparing the physical characteristics of different creatures help us understand evolution?</h3>
To comprehend how living things originated, scientists study the anatomy, embryos, and DNA of various species. Homological structures provide proof of evolution. These are features that were passed down from a common ancestor and are shared by related creatures. An further piece of evidence for evolution is offered by similar structures.
<h3>What role does anatomy play in the study of relationships between various types of organisms?</h3>
Comparative anatomy, which compares structural similarities, is one of the strongest types of evidence of creatures to ascertain the links between them throughout evolution. It is assumed that organisms with similar anatomical traits have evolved from ancestors who were reasonably closely connected to one another.
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<h3><u>Answer;</u></h3>
D. Form part of the cell membrane
<h3><u>Explanation;</u></h3>
- Fats are among the three major nutrients in food, other being proteins and carbohydrates.
- The body uses fat as a source of fuels, and fat is the major storage form of energy in the body.
- Fat has other function such as insulation and protection of vital organs such as the heart and the lungs.
- Fats also acts as chemical messengers helping proteins carry out their functions. Fats are also major components of the cell membrane which regulates materials in and out of the cell.
Answer:
A principle of law stating that within a sequence of undisturbed sedimentary rocks, that the oldest layers are on the bottom and the youngest are on the top. rock layers have a unique set of fossil animal and plant remains which can be used to determine the relative ages of rock layers.
Explanation:
Answer:
Following are the responses to these question:
Explanation:
The heterokaryons were cells of diverse traditions or more nuclei. A heterokaryon cell with network cells (donor and receiver nuclei) sharing a common costly to treat is produced whenever a node containing GFP-tagged protein (donor cell) is merged to a cell non express the GFP-tagged proteins (recipient cell). Unless the intracellular scram nuclear exists, GFP must leave the GFP atoms, be shipped to the cytosol, and be exported to a nucleus with emission of GFP protein (recipient nucleus). It is obtaining nuclear has been beginning to release the GFP protein.
Unless the GFP protein doesn't display a nucleus costly to treat, this is not distributed across time in the metal target. By either sole dissemination through nuclear pores or receptor-mediated routes, protein yelling from nuclear to emotional exhaustion can occur. That GFP proteins are shown in a nucleus only suggests a path via a transmitter. For chloroplast, though, protein disperses via nuclear envelope. It is not the case. It should have nuclear foreign trade signals when ferrying between the nucleus and cytoplasm.
Cycloheximide is indeed a medicine that stops protein expression without elongating. For heterokaryon cells, it inhibits fresh protein synthesis. It makes visualization of a nanoparticle cell of only old pre-existing molecules (before cycloheximide diagnosis). That post GFP substance is a shuttling shielding substance that passes seen between the nucleus and the cytoplasm and the receiver nucleus. Whenever the levels of the shuttle were high, the GFP protein expression is shown both by the sender and receiver nucleus. The recipient nucleus will not be left without any schlepping protein. Thus, the donor nucleus can only be used.
