The organelle where the protein altered in cystic fibrosis is recognized as being abnormal is? Is it endoplasmic reticulum, the Golgi apparatus, lysosome, or the ribosomes or nucleus?
http://en.wikipedia.org/wiki/Cystic_fibrosis
http://www.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/cftr.shtml
Just a little of advice, don't trust wikipedia bc anyone can edit it... and idk the answer srry
To find the correct answer to the question of which organelle recognizes the abnormal protein in cystic fibrosis, we can refer to reliable sources such as scientific articles or reputable websites.
In this case, two sources have been provided: a Wikipedia page on cystic fibrosis and a webpage from the Oak Ridge National Laboratory's Human Genome Project. We can start by examining the information provided in these sources.
According to the Wikipedia page on cystic fibrosis, the genetic mutation that causes cystic fibrosis affects the CFTR (cystic fibrosis transmembrane conductance regulator) protein. This protein is responsible for regulating the flow of salt and fluid in and out of cells. However, the page does not explicitly mention the organelle where the abnormal CFTR protein is recognized as being abnormal.
Next, we can examine the webpage from the Oak Ridge National Laboratory's Human Genome Project. This page describes the CFTR gene and its role in cystic fibrosis. It mentions that the CFTR protein is produced in the endoplasmic reticulum, which is an organelle involved in protein synthesis and folding.
Based on this information, we can conclude that the organelle where the abnormal CFTR protein in cystic fibrosis is recognized as being abnormal is the endoplasmic reticulum.
It is important to note that answers found on the internet may not always be accurate or up-to-date. It is generally recommended to consult multiple reliable sources and keep up with the latest scientific research to ensure accuracy.