swag 6969
In gel electrophoresis, the DNA is placed in wells at one end of the gel. When an electric current is applied, the DNA molecules move through the gel towards the opposite end based on their size. Smaller DNA fragments move faster and travel further through the gel compared to larger fragments.
The DNA is loaded into wells at one end of the gel in gel electrophoresis apparatus. When an electric current is applied, the DNA is separated based on size as it moves through the gel towards the opposite end.
Assuming you're talking about an electrophoresis gel for separating DNA: DNA is itself negatively charged because it contains phosphate groups. Thus, when you apply a current, it will move towards the positive electrode at the other end of the gel. If the DNA were placed at the positive end of the gel, it would migrate backwards and you'd lose the sample.
The comb is placed in slots on the side of the casting tray. It is put in the slots BEFORE the hot, melted gel is poured. After the gel solidifies, the comb is taken out. The "teeth" of the comb leave small holes in the gel that we call "wells."
agarose gel electrophoresis
In gel electrophoresis, the DNA is placed in wells at one end of the gel. When an electric current is applied, the DNA molecules move through the gel towards the opposite end based on their size. Smaller DNA fragments move faster and travel further through the gel compared to larger fragments.
The DNA is loaded into wells at one end of the gel in gel electrophoresis apparatus. When an electric current is applied, the DNA is separated based on size as it moves through the gel towards the opposite end.
Bagel gel Bagel gel Bagel gel Bagel gel
During electrophoresis, DNA samples are placed at the wells of the gel. The gel is then subjected to an electric current, causing the DNA fragments to move through the gel based on their size.
Assuming you're talking about an electrophoresis gel for separating DNA: DNA is itself negatively charged because it contains phosphate groups. Thus, when you apply a current, it will move towards the positive electrode at the other end of the gel. If the DNA were placed at the positive end of the gel, it would migrate backwards and you'd lose the sample.
Gel is the theater term for color filters. These are thin sheets of plastic placed in front of a lighting fixture to color its output.
the chamber has a positive end and a negative end...the DNA moves through the gel toward the positive end (because DNA is negative). The smaller fragments move faster, therefore going further, and the larger pieces stay closer to the wells. what is DNA gel
In gel electrophoresis, DNA fragments migrate toward one end of a gel because they are negatively charged and are attracted to the positive electrode at the opposite end of the gel. The smaller DNA fragments move faster through the gel matrix while the larger fragments move more slowly.
The comb is placed in slots on the side of the casting tray. It is put in the slots BEFORE the hot, melted gel is poured. After the gel solidifies, the comb is taken out. The "teeth" of the comb leave small holes in the gel that we call "wells."
the smallest DNA fragments are observed by a process called elcrophoresis where the DNA fragmnets placed on this gel will migrate according to their lenght so the smallest fragment will migrate the fastest and they will be found at the bottom .
Yes, "gel" and "well" rhyme as they both end in the same sound "-ell."
A period (.) is placed at the end of a declarative sentence.