Answer: Cloning could allow us to produce the perfect human race - one which was hardy enough to withstand all diseases. We could create a world where every human lived to old age without the genes which create psychological or physical problems. and why they are bad because A new study on cloning shows more than ever it's probably a very bad idea to replicate human beings. The study, performed by researchers at the Whitehead Institute for Biomedical Research in Boston, found that cloning to create new animals will almost always create an abnormal creature.
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Biuret Test is the popular test for protein in food.. You will need the food to be tested, an eyedropper, biurets reagent, a test tube or some small container to carry out the biuret test for protein in food. It is important to protect your skin from biuret reagent. It can stain you and other surfaces.
Explanation:
The answer to this question would be lysosome.
Build up of waste material mostly caused by disease in the enzyme that digests the material. Lysosome would be the organ that will hold the material until it was digested. Since it won't digest, the material will be in lysosome forever. The disease itself called lysosomal storage disorder, which was part of the inborn error of metabolism.
Answer:
A (if it is a multi-answer question) also B. Even also C.
Explanation:
C is definitely not the correct answer because germs and microbes are living things and are made of only 1 cell. The cell is also the smallest unit of life because it is called "the building blocks of life", so it has to be the smallest unit of life. Even C, because cells multiply using an existing cell, just like we humans reproduce. First, it duplicates all of its parts, or contents, including the DNA, then they split to create a new cell, (or if i'm incorrect, 2).
Use the chart to help.
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The equivalent magnetization (EM) and mantle Bouguer anomaly (MBA) were calculated along the ultraslow-spreading Mohns Ridge axis in the Norwegian-Greenland Sea. The magnetic anomaly and the associated EM were compared with the bathymetry, MBA, seismically determined crustal structure and geochemical data at both the inter-segment scale (>60 km) and the intra-segment scale (20–60 km). At the inter-segment scale, the magnetic highs at the segment centers are independent of the MBA. Of the 13 segments, 9 with magnetic anomalies >700 nT coincide with axial volcanic ridges identified from multibeam bathymetry maps, which suggests that the magnetic highs at the segment centers may be more associated with the extrusive lavas rather than the amount of magma supply. With few exceptions, the magnetic anomaly lows associated with MBA highs at the segment ends increase from south to north. This trend might be explained by thickened extrusive basalts and/or more serpentinized peridotites at the segment ends in the north. At the intra-segment scale, the most prominent features are the decreases in the magnetic anomalies and associated EMs from the segment centers to the ends. The intra-segment magnetic anomalies have positive and negative correlations with the bathymetry and MBA, respectively. The magnetic signal modeled by the seismically determined layer 2A with an assumed constant magnetization is remarkably consistent with the observed magnetic anomaly, which strongly suggests that the thickness of the extrusive basalts dominates the magnetic structure in each segment along the Mohns Ridge. In general, the thickness of the extrusive basalts dominates the magnetic structure along the Mohns Ridge, whereas the contributions from serpentinized peridotites may be significant at the segment ends and may produce long-wavelength magnetic variations. The magnetic data can be used as an indicator of the thickness of the extrusive basalts within segments along the ultraslow-spreading Mohns Ridge.
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