1. Alkaptonuria an inherited metabolic disorder is due to defiiciency of

Question 1 of 20

2. TATA box is seen in

Question 2 of 20

3. Reducing sugar in urine can be detected by

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4. in well fed state, the activity of CPT-1(Carnitine palmitoyl transferase) in outer mitochondrial membrane is inhibited by

Question 4 of 20

5. in cytochrome P450,P stands for

Question 5 of 20

6. Which of these amino acids does not enter the krebs cycle by forming Acetyl-CoA via pyruvate

Question 6 of 20

7. ketones cannot be utilised by

Question 7 of 20

8. Biotin is required for the activity of

Question 8 of 20

9. Triplex DNA is due to

Question 9 of 20

10. All of the following cell types contain the enzyme telomerase which protects the length of telomeres at the end of chromosomes except

Question 10 of 20

11. ATP is consumed at which step of glycolysis

Question 11 of 20

12. Co-factor for L-amino acid oxidase is

Question 12 of 20

13. which of the following enzymes is common to the synthesis of cholesterol and ketone bodies

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14. Phenyl ketonuria is caused by defective metabolism of

Question 14 of 20

15. Which of the following techniques is used for detection of variation in DNA sequence and Gene expression

Question 15 of 20

16. An example of a preventive antioxidant is

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17. The two fragments of DNA are separated by

Question 17 of 20

18. cell differentiation by surface markers

Question 18 of 20

19. Cabbage-like odour is seen in

Question 19 of 20

20. Edman's reagent is

Question 20 of 20