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Fofino [41]
2 years ago
9

All prokaryotes are _________ eukaryotes

Biology
1 answer:
hjlf2 years ago
4 0
Smaller than eukaryotes
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Which organic molecule is correctly paired with an end product of its break down via hydrolysis?
Gnoma [55]

Answer:

protein - amino acid

Explanation:

Proteins are one of the four major biomolecules in nature. Proteins are polymers of monomeric units called AMINO ACIDS. Amino acids are joined together by a type of covalent bond called PEPTIDE BOND to form proteins. Hence, since proteins are made up of amino acids, the hydrolysis of proteins will result in amino acids.

Hydrolysis is the breaking down of a large polymer into its monomeric unit with the release of water (H2O) molecule as a product. The bonds that forms between the respective amino acids are broken, hence, releasing the amino acids.

3 0
2 years ago
If color blindness is an X-linked recessive trait, what genotype in a father and a mother would be predicted to produce a 1:1 ra
Likurg_2 [28]
The genotype would be X'Y for the father (he would be colorblind)
The genotype would be X'X for the mother (she would be a carrier)
The offspring would be X'X' _ X'X_ X'Y_ XY
The ratio would be 1:1 normal to colorblind
Hope this was helpful(;
3 0
3 years ago
Which of these are not included in the big idea of physical science?
ASHA 777 [7]
What?? what are you trying to say please be more specific
8 0
2 years ago
What are 4 functions of proteins?
Furkat [3]

Answer:

Growth and Maintenance. Share on Pinterest. ...

Causes Biochemical Reactions. ...

Acts as a Messenger. ...

Provides Structure. ...

Maintains Proper pH. ...

Balances Fluids. ...

Bolsters Immune Health. ...

Transports and Stores Nutrients.

8 0
2 years ago
In colorectal cancer, some tumor suppressor genes are inactive. This is an important factor resulting in uncontrolled cell divis
tresset_1 [31]

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

3 0
3 years ago
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