Q. To remove negatively charged molecules through matrix of agarose, nucleic acid molecules are separated by applying

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Q. In genome southern blotting can be used to identify

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Q. Agarose is composed of long unbranched chains of uncharged

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Q. Polyacrylamide gel is usually used for

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Q. In gel electrophoresis the fragments are separated on basis of

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Q. Electromotive force that is used to move the molecules through the gel matrix refers to

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Q. In the buffer nucleic acids are often denatured by using

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Q. Method used for detection of a specific DNA sequence in DNA samples is known as

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Q. For DNA agarose gel have lower

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Q. The positively charged species will migrate towards

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Q. In agarose the proteins are separated by

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Q. When electric current is applied through the gel the large molecules move

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Q. The most common model of enzymatic binding sites is

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Q. The smaller incoming molecule that binds to protein is called

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Q. The total number of binding sites that are occupied by ligands per unit time is called

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Q. The affinity of binding of protein and ligand is chemically

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Q. Most of the binding sites in proteins are

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Q. In induced fit model the substrate interacts with the active site to change it's

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Q. High affinity ligands, which are able to reside in binding site longer have high

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Q. The phenomenon in which the effect of one allele in heterozygous genotype completely masks the effect of other is called

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