<span> Embryonic stem cell research is kind of a dead area now since there is no way to control the differentiation. Most research is being done on adult stem cells to help map and control the differentiation process.
Stem-cells from aborted fetuses - The government doesn't sponsor this, if it is done it is by private companies not located in the USA. You could try researching umbilical cord stem cells to be somewhere near your topic. They come from the afterbirth of normal deliveries.
You could do a much easier report by covering cloning of mice through stem-cell technology. It is happening and helping scientists understand diseases. </span>
Is a technique used to date materials such as rocks or carbon
Plasma, water, salt, protein, platelets
Osmosis is the movement of water particles from an area of high concentration of water particles to an area of low concentration of water particles across a semi permeable membrane
Diffusion is the movement of particles from an area of high concentration of particles to an area of low concentration of particles across a partially permeable membrane
Plasmolysis is the shrinking of the cytoplasm if a plant cell in response to diffusion of water out of the cell and into a high salt concentration solution as the cell membrane would pull away from the cell wall
Hope this helped
Answer:
4 ul Loading Buffer + 19.70 ul dH2O + 0.30 ul DNA Ladder
Load 12 ul on the gel.
Explanation:
DNA Ladder concentration = 1000 ug/ml
1000 ug DNA in 1 ml DNA Ladder solution → 150 ng DNA = 0.15 ug DNA in..... 0.00015 ml = 0.15 ul DNA Ladder solution
6x DNA Loading Buffer → it has to be diluted by an equal volume 6 times (1 ul LB + 1 ul distilled H2O)
An appropriate volume to load on an average agarose gel is 12 ul, so:
2 ul Loading Buffer + 9.85 ul dH2O + 0.15 ul DNA Ladder = 12 ul
But since 0.15 ul is a very small volume and mistakes could be made while measuring it, let's make double:
4 ul Loading Buffer + 19.70 ul dH2O + 0.30 ul DNA Ladder = 24 ul
And load half of that solution (12 ul) on the gel.
