The vitamin that acts as an antioxidant and is important for immune function is: MCQ with Answer and Explanation

The vitamin that acts as an antioxidant and is important for immune function is:
A. Vitamin A
B. Vitamin C
C. Vitamin B₁₂
D. Vitamin K
Answer: Option B
Solution (By JKExamLibrary)
Vitamin C is a potent water-soluble antioxidant, enhances iron absorption, and supports immune cells. Vitamin A also supports immunity but is not primarily an antioxidant; vitamin E is fat-soluble antioxidant.

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Practice More Biology Questions

Question #1
The protein that forms the thick filaments in muscle sarcomeres is:
A. Tropomyosin
B. Troponin
C. Myosin
D. Actin

Correct Answer: Option C


Explanation:
Myosin is the motor protein forming thick filaments; its heads bind to actin thin filaments and generate force via the cross-bridge cycle. Actin forms thin filaments, troponin and tropomyosin regulate contraction. The sliding filament theory describes muscle shortening without filament length change.

This question belongs to: Science Biology
Question #2
Identify the correct statement about evolution:
A. Analogous organs indicate common ancestry.
B. Fossils provide direct evidence of evolution.
C. The human appendix is a homologous organ.
D. Lamarck proposed the theory of natural selection.

Correct Answer: Option B


Explanation:
Fossils are direct evidence showing transitional forms. Lamarck proposed use and disuse, not natural selection. Analogous organs do not indicate common ancestry; homologous do. Appendix is vestigial.

This question belongs to: Science Biology
Question #3
The genetic disorder due to the presence of an extra copy of chromosome 21 is:
A. Turner's syndrome
B. Klinefelter's syndrome
C. Phenylketonuria
D. Down syndrome

Correct Answer: Option D


Explanation:
Down syndrome (trisomy 21) is an autosomal aneuploidy caused by nondisjunction resulting in three copies of chromosome 21. It is characterized by intellectual disability, flat facial profile, protruding tongue, and simian crease. Turner's syndrome is monosomy X (45, X). Klinefelter's is 47, XXY. Phenylketonuria is an inborn error of metabolism (autosomal recessive) due to deficiency of phenylalanine hydroxylase.

This question belongs to: Science Biology