Golgi receives a vesicle containing newly synthesized proteins that were sent by the endoplasmatic reticulum. Then it modifies the proteins and sends them where they need to go.
Explanation:
Protein synthesis is initiated in the cytoplasm when mRNA meets a free ribosome, which is the primary structure for protein synthesis. They read the mRNA code and add the correct amino acid using transference RNA to build the protein. The synthesizing protein is driven to the rough endoplasmic reticulum and translocated to the lumen. Once there, the protein suffers a few modifications, one of them is folding to become functional. Once membrane proteins are folded in the interior of the endoplasmic reticulum, they are <u>packaged into vesicles</u> and <u>sent to the Golgi complex</u>, where it occurs the <em>final association of carbohydrates with proteins</em>. The Golgi complex <u>sends proteins to their different destinies</u>. Proteins destined to a certain place are packaged all together in the same vesicle and sent to the target organ. In the case of membrane proteins, they are packaged in vesicles and sent to the cell membrane where they get incrusted.
The Krebs cycle produces the CO2 that you breath out. This stage produces most of the energy ( 34 ATP molecules, compared to only 2 ATP for glycolysis and 2 ATP for Krebs cycle).
Yes, crossing over does not occur during mitosis. As mitosis is simply the duplication of cells, there is no gene variation that comes from crossing-over.