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julsineya [31]
3 years ago
14

An amino group has what type of properties?

Biology
1 answer:
weqwewe [10]3 years ago
3 0
Hydrophobic<span> is da answer.</span>
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A DNA strand with the sequence A-T-T-G-C-T would be complementary to which of the following? *
STatiana [176]

UAACGA

just so you know T=A/G=C/A=U

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3 years ago
In vertebrates, the embryonic ____ is replaced by tissues that form a vertebral column.
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Notochord

Hope this helps you:)
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What is diabetes insipidus? How would the urine of someone with diabetes insipidus compare to that of someone with diabetes mell
kotykmax [81]

Answer:

In diabetes mellitus, the level of glucose in your blood, also called blood sugar, is too high. Your kidneys try to remove the extra glucose by passing it in your urine. In diabetes insipidus, your blood glucose levels are normal, but your kidneys can't properly concentrate urine.

Explanation:

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Primary succession would occur in which one of the following
GrogVix [38]

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swallow

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eysuusjwhwisijwjeusjsbsbs

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3 years ago
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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

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3 years ago
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