The answer would be thermal insulator, hope it works goodluck
Answer:
1. Liver
2. Liver and Kidneys
3. Mitochondria
4. Lumen of the small intestines
5. Liver
Explanation:
1. Glucose is phosphorylated into glucose-6-phosphate which is the first step of both glycogen synthesis and glycolysis, this process occurs in the liver
2. Glucose 6-phosphate is a product of a process named gluconeogenesis which occurs in the liver it serves as a substrate for glucose-6-phosphatase in the liver.
3. Creatinine kinase is an enzyme that catalyzes the phosphorylation of creatine. In regeneration process of ATP, creatine phosphate transfers a high-energy phosphate to ADP which produces ATP and creatine
4. Initially lipase digestion lipase digestion happens in the small intestine where the bile salts reduce the surface tension of the fat droplets allowing the lipases to attack the triglyceride molecules. These molecules are taken up into the epithelial cells that line the intestinal wall, where they are resynthesized into triglyceride
5. The job of the liver is to produce ketone bodies. If the liver had this enzyme, the ketone bodies it produces would be immediately broken down by the liver before they are released, thereofore, no release of ketone bodies into the bloodstream
To identify people by DNA it is better to make copies of non-coding segments because they exhibit more variation than genes.
- The polymorphic sequences of non-coding DNA vary between individuals in humans.
- Variable number tandem repeats, or VNTRs, are created when DNA sequences are repeatedly replicated in the genome's non-coding regions.
- It is possible to create a person's genetic fingerprint by counting the amount of repeats, which varies between individuals.
- However, this non-coding DNA is used in criminal investigations by forensic experts.
- There are distinctive repeating patterns found inside this area of DNA that can be utilized to distinguish one person from another.
- Short tandem repeats (STRs) are a type of pattern that can be measured to determine a person's DNA profile.
learn more about DNA here: brainly.com/question/21265857
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Answer:
25% or 1/4
Explanation:
The gene for colour in Heliodors is controlled by two contrasting alleles that codes for Red (R) and Yellow (Y) colours. However, these two alleles exhibit incomplete dominance, which is a phenomenon whereby a combination of both alleles gives rise to a third intermediate phenotype that is a blending of the other two parental phenotypes. In this case, both colours gives rise to a heterozygous Orange coloration (RY) in Heliodors.
However, if two orange Heliodors (RY) are crossed, four possible offsprings will be produced with the genotypes: RR, RY, RY, YY. This shows a phenotypic ratio of 1 red: 2orange: 1yellow. Hence, the probability of having a child with red coloration is 1 out of 4 possible offsprings i.e. 1/4.
Expressing this in percentage, we have 1/4 × 100 = 25%.
Answer:
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