Form a hypothesis, Identify a research question or problem, Gather evidence, or data, to test the hypothesis, Analyze the evidence, Decide weather the evidence supports the hypothesis, Communicate the results, Draw conclusions.
Explanation: Because the question is asking to put the project steps in order. Hope this helps :)
Answer:
Hello your question is poorly written, the options and the question is all mixed up but i was able to pick out the correct answer.
answer <em>: A thin liquid layer that is chemically bonded to the interior of a capillary column that comes in contact with an inert carrier gas or mobile phase</em>
Explanation:
The stationary phase in gas Chromatography is best described as ( from the options listed in your question ) :
<em>A thin liquid layer that is chemically bonded to the interior of a capillary column that comes in contact with an inert carrier gas or mobile phase</em>
Gas chromatography is an analytical process used to separate the chemical components ( usually gases ) found in a mixture sample
Answer:B.) Substitution
Explanation: Mutations are permanent changes in the nucleotide sequence of a DNA molecule. Substitution leads to a point mutation if only one nucleotide is replaced by another.
A substitution mutation occurs when one or more nucleotides in a DNA sequence is replaced by another nucleotide.
Example of substitution is in sickle cell hemoglobin in which valine replaces glutamate at position six in the two beta chains of hemoglobin. In a normal hemoglobin, the two beta chains of hemoglobin have glutamate at the sixth position but in a sickle cell hemoglobin, valine is found at position six on the two beta chains. This is also an example of a point mutation.
Ansa million. once you're staring at in ordinary terms one technology, it relatively is, all those fruit flies have been produced via 2 mum and dad, then the only plausible parental genotype that provide you a 50/50 ratio is that if the mummy is XwXw and the father is Xry... this gene is carried on the X chromosome, and w represents white eyes and r represents purple eyes. you are able to bypass forward and draw this out in case you like, even yet it provides 50% heterozygous women individuals (with purple eyes, provided that purple is dominant), and 50% white eyed men, who can in ordinary terms inherit Xw from their mom. The Y that they could inherit from the father could have not any effect on their eye shade. it relatively is comparable for women individuals, they are in a position to in ordinary terms inherit Xw from their mom and an Xr from their father, meaning they'll continually be heterozygous for the attention shade gene. 2. returned, set us the genotypes so which you will visualize it; we are going to say that this disease is carried on the X chrmsm (thats whats usually assumed), and the gene for customary creative and prescient is XB, yet for colorblindness its Xb. those are dominant/recessive to boot. So, if the girl is a provider, her genotype is XBXb, and if the male is colorblind, his genotype is XbY. in case you draw this out in a punett sq., you will get 25% heterozygous woman, 25% colorblind woman, 25% well-known male, and 25% colorblind male. so, there's a 50% risk that any baby they have would be colorblind, 50% risk if its a woman, or 50% risk if it relatively is male.wer:
Explanation:
