Answer:
option A
Explanation:
In carrying out these experimental procedure, the same restriction enzyme that is used to cut out the gene of interest should also be the same used for the cutting of the plasmid to generate sticky ends. Then the desired gene is inserted into the cut plasmid then treatment with DNA ligase. Purified DNA ligase is utilized in gene cloning to join/ligate DNA molecules together forming a recombinant DNA. Thus, step 3 should be carried out after step 4.
Answer:
1/8 (12.5%)
Explanation:
An autosomal recessive disease is an inherited disease in which an individual need to receive both defective alleles at the same gene <em>locus</em> to be expressed in the phenotype. In this case, both parents are carriers of the recessive mutant allele associated with the sickle cell anaemia trait, thereby both parents are heterozygous, ie., each parent has one copy of the normal allele 'H' and one copy of the defective mutant allele 'h' associated with this condition. In consequence, their first child has a 1/4 (25%) chance of having sickle-cell anaemia. Moreover, the chance of having a girl is 1/2 and the chance of having a boy is 1/2, thereby the final chance of having a girl sickle cell anaemia individual is 1/4 x 1/2 = 1/8 (12.5%).
- Parental cross for sickle cell anaemia trait = Hh x Hh >>
- F1 = 1/4 HH (normal); 1/2 Hh (normal); 1/4 hh (sickle cell anaemia) >>
- Sex proportion of sickle cell anaemia individuals = 1/8 female sickle cell anaemia individuals + 1/8 male sickle cell anaemia individuals (1/8 + 1/8 = 1/4)
A cellular membrane separates the interior of all cells from the outside environment.
The first step to DNA replication is to unzip the double matrix which also means that they will break the double matrix.
Answer:
White blood cells ↓
These are donut-shaped cells that are similar to red blood cells, and do have a similar duty, yet are larger.