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Serhud [2]
3 years ago
12

What happens during translation?

Biology
1 answer:
victus00 [196]3 years ago
6 0

Answer:

A ribosome uses the sequence of codons in mRNA to assemble amino acids into a polypeptide chain.

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A possible explanation, or ____________________, may be tested by experimentation.
wlad13 [49]
Hypothesis or prediction or theory
8 0
3 years ago
Read 2 more answers
In humans, the allele for red-green color blindness is X-linked and recessive (Xr; the dominant allele is called XR). A man with
taurus [48]

Answer:

It concludes that the man is not the real father of the girl child.

Explanation:

Sex-linked or the X linked characters are the traits that inherited in a change or mutation in X chromosomes that cause the phenotype change in the male, which are homozygous for the gene as only possess one X chromosome and one Y chromosome, and Females if they are homozygous for the gene.

In the question, Man has a normal color vision (XrY) that means he has no mutated allele of color blindness. female has color blindness so that means she is a homozygous chromosome for the gene. Cross between these two results in 50% carrier daughters (XrXR) and 50% color blindness son (XRY). It means there is no chance for the color blind daughter.

Thus, the correct answer would be the man is not the real father of the girl child.

8 0
3 years ago
what will be the sex of a child produced when an egg is fertilized by a sperm that has a y chromosome
Alex787 [66]
Men have xy and women have xx chromosomes. the mens sperm is the chromosome that determines the sex of the child. x is female and y is male so the answer is male
3 0
4 years ago
A mutation is any mistake or change in the
katrin [286]

Answer:

zygote

Explanation:

or the mode of reproduction

3 0
3 years ago
In 1-2 sentences, describe what a sequence-tagged site (STS) is and how STSs are used in genome sequencing.
Ede4ka [16]

Answer:

STS are short stretches of DNA used for producing genomic map

Explanation:

Sequence tagged sites (STS) are primers that possess some form of sequence knowledge and are used to produce genetic maps through standard mapping procedure. STS primers are short replica or stretch of DNA which is detected by using PCR array.

These STS primers are unique and sequence specific and thus are responsible for detecting variations in genomic DNA and can also distinguish between homozygotes and heterozygotes.  

3 0
4 years ago
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