Explanation:
Gel electrophoresis is one simple and cheap laboratory technique used in profiling. In this case, it can be used to identify Great White Sharks using their proteins or DNA. This way, even if the fish is completely mutilated into the meat, the species can still be identified helping policies to be enforced.
DNA or proteins of a sample of suspected meat is processed and passed through gel electrophoresis. The bands that form are then compared with a standard to check if the bands match. A match indicates that the meat is from a Great White Shark.
In a cladogram the tiny indentations along the bottom line is an evolution or change and every organism after the indentation on the bottom line has it and every organism before the indentation does not
Answer:
The correct answer is <u>False</u>
Explanation:
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Answer:
Angle of isolation.
Explanation:
If the Earth was flat all the rays would strike it at 90 degrees.
Answer and Explanation:
Ribosomes are the primary structure for protein synthesis. They can be found in the rough endoplasmic reticulum or floating in the cytosol.
Free ribosomes are not attached to any cytoplasmic structure or organelle. They synthesize proteins only for internal cell use. Other ribosomes are attached to the membrane of the endoplasmic reticulum and they are in charge of synthesizing membrane proteins or exportation proteins. Free and attached ribosomes are identical and they can alternate their location. This means that although free ribosomes are floating in the cytosol, eventually, they can get attached to the endoplasmic reticulum membrane.
Synthesis of proteins that are destined to membrane or exportation starts in the cytoplasm with the production of a molecule portion known as a <u>signal aminoacidic sequence</u>. This signal sequence varies between 13 and 36 amino acids, is located in the <u>amino extreme</u> of the synthesizing protein, and when it reaches a certain length, it meets the <u>signal recognizing particle</u>. This particle joins the signal sequence of the protein and leads the synthesizing protein and associated ribosome to a specific region in the Rough endoplasmic reticulum where it continues the protein building. When they reach the membrane of the endoplasmic reticulum, the signal recognizing particle links to a receptor associated with a pore. Meanwhile, the ribosome keeps synthesizing the protein, and the enlarged polypeptidic chain goes forward the reticulum lumen through the pore. While this is happening, another enzyme cuts the signal sequence, an action that requires energy from the ATP hydrolysis. When the new protein synthesis is complete, the polypeptide is released into the reticulum lumen. Here it also happens the protein folding (which is possible by the formation of disulfide bridges of proteins are formed) and the initial stages of glycosylation (the oligosaccharide addition).
Once membrane proteins are folded in the interior of the endoplasmic reticulum, they are packaged into vesicles and sent to the Golgi complex, where it occurs the final association of carbohydrates with proteins. The Golgi complex sends proteins to their different destinies. Proteins destined to a certain place are packaged all together in the same vesicle and sent to the target organelle. In the case of membrane proteins, they are packaged in vesicles and sent to the cell membrane where they get incrusted.
There are certain signal sequences in the <u>carboxy-terminal extreme</u> of the protein that plays an important role during the transport of membrane proteins. A signal as simple as one amino acid in the c-terminal extreme is responsible for the correct transport of the molecule through the whole traject until it reaches the membrane.
