Answer:
In this ELISA procedure, a sample of protein is immobilized in the plastic well and then antibody for this protein added and incubated, and cleared out. In the given setting detection, the antibody is conjugated with the protein of interest and if the substrate molecule added to the reaction it will produce a colored product by reacting with the enzyme.
No reaction will take place in the well in case of not adding secondary antibody or detection antibody to the reaction and no colored product will be received.
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Answer:
The fragment and plasmid are both cut with the same restriction enzyme.
Explanation:
To insert a piece of DNA in a bacterial plasmid, we need to cut both plasmid and DNA insert from same regions. This is typically done by restriction enzymes or restriction endonuclease. This cutting will open the plasmid (which is circular initially) and produce <u>sticky ends.</u> Here, DNA insert can attach because of similar sequence (see attached figure). In the final step, DNA ligase will glue it in the plasmid and it will become its part. This technique has been extensively used as a DNA recombinant technology. A better representation can be seen in the attached figure where both DNA sequence of interest and plasmid are cut with the same restriction enzyme (shown as scissors) and then ligated with DNA ligase.
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It produces the silk that use to make clothes