How can the binding assay approach be utilized to match coding triplets with their amino acid counterparts?

What is the purpose of hydrolyzing the RNA before conducting biochemical tests?

How can these designed nucleases modify the sequence of genomic DNA?

In a competitive RNA microarray experiment, you hybridize two samples to the same chip.  Before hybridization, sample A is labeled with red fluorescence and Sample B is labeled with green fluorescence.  Spot 1142 is yellow.  What does this tell you about the relative abundance of the mRNA corresponding to this spot in the two samples? Group of answer choices It is equally abundant in both samples A and B. It is more abundant in B than A. It is more abundant in A than B. It is not present in either A or B.

How is the Bicinchoninic acid assay used in protein quantification?

How do you design a reporter assay for Serpina1?

Gene expression can be disrupted by techniques such as homologous recombination and RNA interference. What is the functional difference between these two methods in terms of the ultimate effect on gene expression? Why might homologous recombination or an alternative genome-editing method (e.g., CRISPR/Cas9) be preferred over RNA interference?

What is the functional significance of sticky ends in a cloningexperiment?What type of bonding makes the ends sticky?

Design a six-residue nucleic acid probe that would hybridize with the greatest number of E. coli gene promoters.

What do you expect to see in a protein truncation test when there is a nonsense mutation? What do you expect to see in a protein truncation test when there is a nonsense mutation? there will be no signal from the mutated protein the mutated protein will be less abundant (have a weaker signal) that the regular protein the mutated protein will be shorter than the regular protein there will be two bands on the gel for the mutated protein