Answer:
The physical infrastructure for X-ray crystallography structural biology includes synchrotrons, which are affordable by a nation. There are 47 in the world (lightsources.org). Each synchrotron provides a number of beamlines for experiments, usually including several optimized for macromolecular X-ray crystallography, often some for other structural biology techniques including SAXS (Small-Angle X-Ray Scattering) and CD (Circular Dichroism), and usually some beamlines for material sciences and other non-biological applications.
Explanation:
https://www.creative-biostructure.com/Data-Processing-and-Interpretation-584.htm
Answer:
The ear length will be 11 cm.
Explanation:
To know about the ear length of F1 generation, we need to know that how much length in centimeters is contributed by each of the alleles. As we know, each allele has the same value for contributing to the effect of ear length, hence we can divide the ear length by 4 to get our results.
As 6 divided by 4 is 1.5 hence, the allele a and b contribute to 1.5 cm of the length of the ear.
6 divided by 4 is 4, hence the alleles And B contribute to 4 cm of the length of the ear.
The F1 generation will have AaBb genotype hence, the lenght will be 4+1.5+4+1.5 = 11 cm.
Answer:0.8775
Explanation:formula for gene frequency is p+q=1
where p is the dominant allele and q is the recess allele.
Given than p=0.35
P^2=0.35^2=0.1225
q=1-p
q=1-0.1225=0.8775
Answer is 0.8775
Answer: B. Melting temperatures of primer should be between 55-80 degree Celsius.
Explanation:
Bacause the melting temperature controls the binding of the primers to your template DNA. At melting temperature 50% of the primer molecules are bound to their corresponding target sequence. If the difference in melting temperature between the two primers is too high, it might be difficult to find experimental conditions where both primers can bind to their target.
