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erica [24]
3 years ago
12

Below is the base sequence on one side of a DNA molecule. What would the complimentary side of this strand of DNA read? ATC TCA

GAT CGT CAG
UAG AGA GUA CGA GUC
AUC UCA GAU CGU CAG
ATC TCA GAT CGT CAG
TAG AGT CTA GCA GTC
Biology
1 answer:
Agata [3.3K]3 years ago
7 0

Answer:

nongenima

Explanation:

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For each of the following features of nucleic acids, indicate whether it is true of DNA only, of RNA only, of both DNA and RNA,
suter [353]

Answer:

Nucleic acid is one of the four major macromolecules that is present in all life forms. It includes DNA ( deoxyribonucleic acid) and RNA (ribonucleic acid). It is made up of small unit called nucleotides.

A nucleotide contains a pentose sugar that is deoxyribose in DNA and ribose in RNA, nitrogenous base that is Adenine, Thymine, Cytosine, Guanine in DNA and Adenine, Uracil, Cytosine, Guanine in RNA, and a phosphate group.

It is synthesised by a process of comlementary base pairing ( such as in double stranded DNA, A pairs with T and G pairs with C).

DNA is converted to mRNA inside the nucleus of eukaryotic cell and mRNA is then translated to protein when it moves the cytosplasm of the cell.

Thus, the correct answers are as follows-

1) Is an inherently directional molecule, with an N-Terminus on one end and a C-Terminus on the other end - true neither for RNA or DNA.

2) Contains the base adenine- True for both DNA and RNA.

3) Contains the nucleotide deoxythmidine monophosphate- True for DNA

4) Occurs only in signle stranded form- True for both RNA and DNA( such as single stranded DNA in DNA virus, and RNA in single stranded RNA in AIDS virus).

5) Is synthesized by a process that involves base pairing- True for both DNA and RNA.

6) Is involved in the process of protein synthesis in the cytoplasm of the cells in the liver- True for RNA ( particularly messenger RNA, mRNA)

3 0
3 years ago
Read 2 more answers
Historically, physicians have used a procedure called xenodiagnosis to diagnose which of the following diseases?A. schistosomias
Mrac [35]

Answer: C. Chagas disease

Explanation:

Xenodiagnosis is a method of diagnosis and detection of the microorganism responsible for infecting the tissues of the body.

Chagas disease is a potentially life threatening disease. It is caused by the protozoan parasite called as Trypanosoma cruzi. It is transmitted to people through the feces of insects. This disease is common in South and Central America and in Mexico. The xenodiagnosis is used to detect the parasite responsible for the Chagas disease.

5 0
3 years ago
Provide TWO reasons why the genotype and phenotype frequencies do not match in the Tadjik population. (Hint: Think about the met
Viktor [21]

Answer:

The reason why the genotype and phenotype frequences do not match is just because the 1) The genotype based on genes observation,while the phenotype based on physical appearance of the organism externally

Explanation:

the genotype is looking on the arrangement of genes in pair and get its frequency ,while phenotype the external physical appearance of organism is observed to get frequency

4 0
3 years ago
What is a stinging cell that is a distinguishing feature of all cnidarians
ASHA 777 [7]
Cnidarians have specialized cells known as cnidocytes (“stinging cells”) containing organelles called nematocysts. These cells are concentrated around the mouth and tentacles of the animal and can immobilize prey with toxins. Nematocysts contain coiled threads that may bear barbs.
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3 years ago
Why choose that gene for PCR in the bacterial identification lab?
Reika [66]

Answer:

Background

During the course of a bacterial infection, the rapid identification of the causative agent(s) is necessary for the determination of effective treatment options. We have developed a method based on a modified broad-range PCR and an oligonucleotide microarray for the simultaneous detection and identification of 12 bacterial pathogens at the species level. The broad-range PCR primer mixture was designed using conserved regions of the bacterial topoisomerase genes gyrB and parE. The primer design allowed the use of a novel DNA amplification method, which produced labeled, single-stranded DNA suitable for microarray hybridization. The probes on the microarray were designed from the alignments of species- or genus-specific variable regions of the gyrB and parE genes flanked by the primers. We included mecA-specific primers and probes in the same assay to indicate the presence of methicillin resistance in the bacterial species. The feasibility of this assay in routine diagnostic testing was evaluated using 146 blood culture positive and 40 blood culture negative samples.

Explanation:

Results

Comparison of our results with those of a conventional culture-based method revealed a sensitivity of 96% (initial sensitivity of 82%) and specificity of 98%. Furthermore, only one cross-reaction was observed upon investigating 102 culture isolates from 70 untargeted bacteria. The total assay time was only three hours, including the time required for the DNA extraction, PCR and microarray steps in sequence.

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