Answer:
e. None of the above
Explanation:
For me as a Researcher, the reason could be increased Concentration of your DNA sample which you are using as your template. Try to decrease the concentration of DNA (up to 100 ng per reaction is enough and can increase up to 200 ng). so the reason for getting non specific bands is increase concentration of DNA which results in non specific amplification and also degradation of DNA in the reaction which you can see in your gel electrophoresis results.
i always corrected my results using the same technique that is lowering the concentration of DNA between 100 and 200 ng per single reaction of PCR.
The monosaccharides that are produced when sucrose is digested would be glucose and fructose.
Answer:
O founder's effect
Explanation:
A founder effect can be defined as the loss of genetic variation when a new population is established from a few individuals. This process is known to increase the frequency of particular gene variants (alleles) at different <em>loci</em> when they are selectively neutral (or nearly neutral), and thereby such genes are fixed by genetic drift (i.e., through the random sampling of founder individuals). Interestingly, it has been discovered that the majority of South American and Central American Indians are nearly exclusively in the O blood group, which has been further associated with random genetic drift and a founder effect.
Answer:
There you go! they explained it better than I could. hopefully that helps you, for more information you could simply look up an article.
Answer:Rarely use plastic
Explanation: