Electric cars and the renewable energy that create the electricity to charge
them protects environmental quality.
Renewable energy arise from renewable sources such as sunlight, wind etc
and they are always replenished from time to time. This form of energy
doesn't emit compounds such as greenhouse gases thus helping to protect
environmental quality.
Non renewable energy is mostly gotten from fossil fuels which emits carbon
and other compounds . These compounds pollute and reduces
environmental quality.
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<h2>Answer:</h2>
As in a given cross two genes control the height and flower color. Tall height (T) is dominant over the short height (t) and yellow flowers (Y) are dominant over the white flower (y).
When the tall yellow flowered mated with short white flowers, the genotype of the plants can be;
TTYY × ttyy or It can be TtYy × ttyy or TTYy × ttyy or TtYY × ttyy
The answer is D. Nighttime
Answer: 3. adenine (A, green), thymine (T, red), cytosine (C, orange), and guanine (G, blue). 4. adenine (A), cytosine (C), and guanine (G) — are also found in DNA. 5. A nucleotide consists of a sugar molecule (either ribose in RNA or deoxyribose in DNA) attached to a phosphate group and a nitrogen-containing base. The bases used in DNA are adenine (A), cytosine (C), guanine (G), and thymine (T). 6. food crops like soy and corn that have been genetically modified for pest and herbicide resistance. These crops are widely known as “GMOs” (genetically modified organisms). 7. There are two differences that distinguish DNA from RNA: (a) RNA contains the sugar ribose, while DNA contains the slightly different sugar deoxyribose (a type of ribose that lacks one oxygen atom), and (b) RNA has the nucleobase uracil while DNA contains thymine. brainliest?
Explanation:
Answer/Explanation:
(1) a mutation in the coding region, resulting in an inactive protein
To check to see if there is a mutation, you could extract the DNA from the cancer cells and then perform PCR to amplify the gene of interest. You could then perform sanger sequencing and compare the sequence to the normal gene to see if a mutation is present. To test the effect of the mutation, you would want to see if an active protein has been formed.
To see if a normal sized protein has been formed, you could perform a western blot, comparing the protein band to the WT protein band. If the protein is absent or much smaller, it is likely not a functional protein.
(2) epigenetic silencing at the promoter of the gene, resulting in reduced transcription.
To check for changes in the epigenetic landscape of the promoter, you could perform chromatin immunoprecipitation by extracting the chromatin from the tumour cells and using antibodies for different chromatin marks to see what has changed between the normal cells and the tumor cells. E.g. H3K9me3, H3K27me3. You would perform a pull down with the antibody of interest and then PCR for your promoter to specifically look at changes at that gene compared to normal cells. To test DNA methylation, you could perform bisulfite sequencing.
To see how transcription is affected, you could extract RNA from the tumor and normal cells, and compare the levels of RNA between the two samples by qRT-PCR
