Answer: i would say the answer is D
Explanation: srry if i got it wrong
Answer:
E. Gene is amplified by multiplication of cloning host
Explanation:
PCR is a very powerful technique that can help us to amplify exponentially one gene from a very small sample of DNA.
As seen in the attached image, the process begins with a single DNA molecule, for the first cycle, that DNA molecule denaturalizes into two strands, the primers bind to their complementary sides and then the DNA polymerase builds the new DNA strands. The number of copies of the gene that can be obtained with each cycle are 2ⁿ copies, where n is the cycle number.
Answer:
In eukaryotic cells you find core and proximal promoters.
Promotors are specific DNA sequences where transcription factors (proteins) and RNA polymerase binds to initiate transcription. Promotors are located upstream the coding sequence
Core promoters are where RNA polymersae binds and proximal promoters are where transcription factors bind.
Enhancer elements are DNA sequences where transcription factors (proteins) bind to increase the rate of expresion of an specific gene. Enhancers can be located either upstream, downstream or thousands of nucleotids away from the of the coding region.
Explanation:
Promoters and enhancer are key elements for controling gene regulation. Transcription begins when chromatin rearranges from a condensed state to a accesible state, this allow to transcrition factors and RNA polymerase to bind specif DNA sequences (promotors). Proteins bind to enhancers , this complex develops a DNA loop, so that the protein that is bound to the enhancer interacts with the RNA polymersase. When this interaction is made, the activity of the RNA polymerase is increased.
The outer core is less dense than the B.)inner core. This because there is more pressure on the inner core resulting in a higher density. This increased pressure even makes it solid versus the liquid outer core.
