It is important to know how we can understand the limits of the possibilities of Genetic Engineering, the problem is a problem of numbers. Contains rights of the (DNA) is enough to make one million gene Genetic Engineering but considering only one gene, then there is the problem of identification of this gene.How do we know this gene among other genes?Will be the first step is making the so-called "carrier molecule" and this works Dzie Assistant bearer carries the desired gene into the cell and helps to double the gene itself (which is similar to the person carrying the disease is hereditary in the USA that the person holds a gene without affecting it).
The carrier is a small piece of the (DNA) can double Ikvah within the cell itself needs to be a small piece because of the large pieces (DNA) is not easily dealt with in the tube. Also needs to be high efficiency in replication because we need a lot of them.Natural that all the (DNA) that can double the existence of the same enzyme which facilitates this process an enzyme polymerization. The (DNA) enzyme helps to follow the rules and needs to be compounded by signal (Start here).To avoid the confusion that occurs when there are molecules of the two enzymes for the polymerization of the (DNA) in opposite directions trying to Inskha the same molecule. Permission was needed to contain such a reference carrier if it is to become useful to us.We have a carrier and would now like to Nolg by Gina. Must isolate the section of the (DNA) do not only contain a gene that we want.Remained the problem intractable for many years was not because of the impossibility of breaking pieces of the (DNA) long into small pieces (in fact, that the molecules (DNA) too, which is found in human cells molecules ostrich even ripped into small pieces once Tdlq of the tube to another) . But our purpose is not once breaking the (DNA) to spare, but we want these pieces to agreeThe carrier molecule, as we re-correct form so that it can reach the parts again in harmony.The rules of the (DNA) cost of chemicals with the rules of complementary and that if our class series double helix, this attraction between two bases complementary will bring them again to each other and the attraction of the rules of complementary is the basis for multiplying the self of the (DNA) and the small pieces made by an enzyme specifically pregnancies also rules are not accompanied by complementary Brafiqtha that is, "without further series" of the (DNA) relate. It picks up free complementary rules are not enough. But there are rules available to them and even have the same sequence required to form a series of complementary rules associated with - there are rules on the extrusion short single chain that stands out from the other party the lump-so and so extrusion short single chain that stands out from the other party the lump-so and so Alnwightn have resulted from cutting the same molecule must necessarily would carry complementary rules. Thus, the solution is simple - the only two sections are drawn on both sides Almoktuaan series to each other again. Because the parties to the (DNA) their parts protruding so tend to stick again after amputation, they are called "parties sticky" and a link to the parties is not a sticky solid. We must not forget that any enzyme identification always give the same parties sticky that is important in cutting or pasting is a short sequence of rules and not Mabinha of rules. This is exactly what the USA needs a genetic engineer.
التسميات
Inheritance