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DNA sequencing is a technique used to determine the exact sequence of nucleotides in a DNA sample. Electrophoresis, a method for separating DNA fragments, is used when the DNA differs in length by only one base. DNA samples are placed in a gel and exposed to an electric...


Plant cells do have DNA. All living things known by science use DNA as their genetic code. Like almost all living things, plants are eukaryotes, which are defined by their membrane-bound nucleus and other organelles.


DNA is found in the nucleus of animal cells. The DNA compounds are packaged into chromosomes inside the nucleus. Each chromosome contains a single molecule of DNA that can be replicated during the processes of transcription and translation.


The human genome present in the nucleus of nearly all cells within the body is composed of 3.2 billion base pairs. If unwound, this DNA would stretch to about 6 feet.


The cell nucleus controls most cell processes and contains DNA. The nuclear envelope surrounds the nucleus and contains pores, which regulate what goes in and out of this control center.


DNA, or deoxyribonucleic acid, is used in the human body in order for an organism to reproduce, develop and survive as well as in science for genetic engineering, forensics, bioinformatics, evolutionary history and information storage. A human's DNA code contains about ...


The majority of DNA is located in the cell nucleus, where it is called nuclear DNA. A small amount is located in the mitochondria, where it is called mitochondrial DNA.


DNA is made of repeating units called nucleotides. The four nucleotides in DNA are adenine, cytosine, guanine and thymine. Adenine binds with thymine, and guanine binds with cytosine.


The sequence of the cell cycle is G1, S, G2, mitosis and cytokinesis. G1 and G2 are "gap" phases during which the cell grows and prepares for other phases. The S phase is the stage when DNA is copied. Mitosis divides the copies of DNA, and cytokinesis creates two new ce...


Wageningen University explains that DNA bases only pair with one other base, so the complementary DNA sequence can be read out by replacing each base with its complement and reversing the order. The complementary base pairs are A to T and G to C, so every G is replaced ...