a. Plasmid DNA and chromosomal DNA
| Plasmid DNA | Chromosomal DNA |
| Plasmid DNA is an extra-chromosomal DNA molecule in bacteria that is capable of replicating, independent of chromosomal DNA | Chromosomal DNA is the entire DNA of an organism present inside chromosomes |
b. RNA and DNA
| RNA | DNA | |
| 1. | . RNA is a single stranded molecule | DNA is a double stranded molecule. |
| 2. | It contains ribose sugar. | It contains deoxyribose sugar. |
| 3. | The pyrimidines in RNA are adenine and uracil. | The pyrimidines in DNA are adenine and thymine. |
| 4. | RNA cannot replicate itself. | DNA molecules have the ability to replicate. |
| 5. | It is a component of the ribosomes. | It is a component of the chromosomes. |
c. ) Exonuclease and Endonuclease
| Exonuclease | Endonuclease |
| It is a type of restriction enzyme that removes the nucleotide from 5' or 3' ends of the DNA molecule. | It is a type of restriction enzyme that makes a cut within the DNA at a specific site to generate sticky ends |
Match the technique with its application. 
Match sequencing methods with key feature. 
In an economy, the currency held by the public, Net Demand Deposits with Commercial Banks and Net Time Deposits with Commercial Banks stand at ₹ 1,42,000 crore, ₹ 22,000 crore and ₹ 86,000 crore respectively. The value of Money Supply (M1) would be ₹ _______ crore.
In an economy, when __________ is insufficient to achieve the level of output corresponding to the full employment, the difference is termed a deflationary gap.
In an economy, exclusion of _______ may lead to under estimation of the value of Gross Domestic Product (GDP).
“In the Indian Banking System, the Statutory Liquidity Ratio (SLR) plays a vital role in controlling the credit creation capacity of the Commercial Banks, as it _______”
In a two sector economy, the flow of factor payments moves from ________ to _________.
Recombinant DNA technology is the process used for producing new genetic combinations by joining different genetic material (DNA) together and inserting them into host organisms from two different species or sources. These new combinations are of value to medicine, science, industry, and agriculture.
Step 1- Isolation of Genetic Material.
Step 2- Cutting the gene at the recognition sites.
Step 3- Amplifying the gene copies through Polymerase chain reaction ( PCR)
Step 4- Ligation of DNA Molecules.
Step 5- Insertion of Recombinant DNA into Host.