Written by students who passed Immediately available after payment Read online or as PDF Wrong document? Swap it for free 4.6 TrustPilot
logo-home
Document preview thumbnail
Preview 2 out of 9 pages
Exam (elaborations)

C785 Final BIOCHEM Exam Questions and Answers

Document preview thumbnail
Preview 2 out of 9 pages

C785 Final BIOCHEM Exam Questions and Answers

Content preview

C785 Final BIOCHEM Exam Questions
and Answers




Which mRNA sequence results in a polypeptide that contains three amino acids? - Answer-5' - CUU GAU
ACU UAG - 3'



Which RNA sequence would end in the following polypeptide?



Phe-Thr-Val-Stop - Answer-5' - UUC ACA GUA UAA - 3'



What is the complementary sequence for the following DNA sequence?



5' - GCC ATC TCG AAT - 3' - Answer-5' - ATT CGA GAT GGC - 3'



Assuming 100% reaction efficiency, how many DNA copies are created after the completion of four
complete PCR cycles? - Answer-16



What is the function of DNA polymerase in the process of PCR? - Answer-It recognizes the primers and
uses the available dNTPs to replicate the template DNA sequence.

, 5' - [...] ATT CGC TAG GGC [...] - 3' − Normal DNA

5' - [...] ATT CGC GAG GGC [...] - 3' − Mutant DNA



Which type of mutation and outcome characterizes the Mutant DNA? - Answer-A missense mutation
leading to a longer protein



In sickle-cell disease, the glutamic acid (Glu) at position number seven is mutated to valine (Val).



What change in codons corresponds to this mutation? - Answer-GAA to GTA



What are possible blood types of the parents of a patient with blood type AB? - Answer-A and B



Which pair of chromosomes accurately depicts the genotype of a person with an autosomal recessive
mutant HBB allele and sickle cell anemia? - Answer-option 3- 2 mutant genes on chromosome 11



Which pair of chromosomes accurately depicts the genotype of a person with an X-linked recessive
mutant ALAS2 allele and sideroblastic anemia? - Answer-option 3, mutated allele



Studies have shown that increased expression of two genes called SIRT1 and SIRT2 is associated with
chronic exposure to cocaine and contributes to drug addiction.



What difference in the regions of the SIRT1 and SIRT2 genes in people addicted to cocaine increases
their expression? - Answer-The nucleosomes become more widely spaced.



Mice with low levels of agouti gene expression tend to have yellow fur and are obese, while mice with
higher levels of expression are brown and of normal weight. Studies show that expression of the agouti
gene in mice can be controlled by epigenetics.

Document information

Uploaded on
December 3, 2024
Number of pages
9
Written in
2024/2025
Type
Exam (elaborations)
Contains
Questions & answers
$14.49

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
Zanaya
4.5
(12)
Sold
78
Followers
29
Items
10176
Last sold
5 days ago



Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions