Answer:
The correct answer is -
A) BbTt x bbTt
B) .5^4 or 1/16 or 0.0625
Explanation:
As it is given that Brachydactylus and PTC tasters both traits are autosomal dominant conditions which mean only one allele would be enough.
For Branchydactylus and For tasting : man and women will be heterogeneous.
Hence,
The Genotype of man = BbTt
The Genotype of wife = bbTt
b. Answer = 0.0625
For Branchydactylus:
Bb X bb
Possible genotypes:
B b
b Bb( Brachydactylus) bb(normal)
b Bb (Brachydactylus) bb (normal)
The probability of a single child being Branchydactylus = 2/4 = 0.5
So, Probability of all 4 child being Branchydactylus = .5 x .5 x .5 x .5 = 0.0625
Genetic fingerprinting – the analysis of DNA in order to identify the individual from which the DNA was taken to establish the genetic relatedness of individuals. It is now commonly used in forensic science (for example to identify someone from a blood sample) and to determine whether individuals of endangered species in captivity have been bred or captured from the wild.
<span>•DNA sequencing – the determination of the precise sequence of nucleotides in a sample of DNA or even a whole genome e.g. the Human Genome Project. </span>
<span>The process of electrophoresis: </span>
<span>DNA is chopped, close to the VNTR regions, into fragments using restriction enzymes. The DNA fragments are placed on the agarose gel and a direct current is applied continuously to the gel. The DNA fragments are attracted to the anode. The shorter the fragment, the faster it moves. </span>
<span>The fragments are transferred onto an absorbent paper placed on top of the gel. The paper is heated to separate the 2 strands in each DNA molecule. Complementary probes which have a radioactive phosphorus isotope are and this pair up with the DNA strands. The paper is placed on an X-ray film and the film goes dark due to radiation emitted by the probes. Now we end up with a pattern of dark stripes on the film matching the positions reached by the fragments in the agarose gel.</span>
Answer:
DNA synthesis occurs in the 5′ → 3′ direction only and requires a large suite of specialized enzymes.
Explanation:
This Does not look like a qustion may you please take it down
Answer:
This definition suits that of "HOMOLOGOUS CHROMOSOMES"
Explanation:
Homologous chromosomes are similar pairs of chromosomes i.e. in length, gene positioning and centromere location (one from each parent) but not identical. Homologous chromosomes are not identical in the sense that, alleles on each pair may be different, resulting in genetic variation of the offspring.
Using humans as a case study, a karyotype (pictorial display of chromosomal arrangement) shows the complete set of chromosomes, which has two complete set (diploid). Each human cell contain 23 pairs of chromosomes, with each pair contributed by each parent i.e. 46 chromosomes in total. Every chromosome pair represents a set of homologous chromosome.
