Q.48 The amount of agarose required to prepare 250 ππΏ of 0.8% agarose gel
is __________ πππππ (rounded off to the nearest integer).
2 grams of agarose are required to prepare 250 mL of 0.8% agarose gel. This calculation uses the standard weight/volume (w/v) formula for gel concentration, rounded to the nearest integer.β
Calculation Method
Agarose gel percentage is defined as grams of agarose per 100 mL of buffer (w/v). For 0.8%, dissolve 0.8 g agarose in 100 mL buffer.β
Scale proportionally: Mass (g) = (0.8 / 100) Γ 250 mL = 2.0 g.β
Round 2.0 to the nearest integer: 2 g.
Step-by-Step Preparation
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Weigh 2 g agarose powder.β
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Add to ~200 mL electrophoresis buffer (TAE or TBE) in a flask.β
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Microwave to dissolve (swirl to avoid boiling), cool to ~60Β°C, add dye if needed, pour into gel tray.β
A 0.8% gel suits DNA fragments of 1β10 kb.β
Agarose Gel Concentrations
| Gel % | DNA Size Range (bp) | Common Use |
|---|---|---|
| 0.5% | 2,000β50,000 | Large fragments |
| 0.8% | 1,000β10,000 | PCR products, plasmids |
| 1.0% | 400β8,000 | Routine DNA |
| 2.0% | 100β2,000 | Small fragments |
CSIR NET Exam Context
This fill-in-the-blank question tests precise calculation skills for molecular biology techniques. No options provided; direct computation yields 2 g. Verify units (mL, %, g) to avoid errors like confusing v/w.β
Agarose gel electrophoresis remains essential in molecular biology for DNA separation, andΒ agarose gel calculationΒ for precise concentrations likeΒ 0.8% agarose gelΒ is a core skill for CSIR NET aspirants. This guide solves “amount of agarose required to prepare 250 mL of 0.8% agarose gel” with detailed math, protocol, and exam tips.β
Agarose Percentage Explained
Agarose gel concentrationΒ uses w/v: 0.8% = 0.8 g per 100 mL buffer. Higher % creates smaller pores for better small-fragment resolution; 0.8% excels for 1β10 kb DNA. Common range: 0.5β2%.β
Exact Calculation for 250 mL 0.8% Gel
Formula: Mass (g) = (% / 100) Γ Volume (mL)
= (0.8 / 100) Γ 250 =Β 2.0 gΒ (rounds toΒ 2 grams).β
Pro Tip: Use analytical balance; errors in scaling lead to poor resolution.β
Full Preparation Protocol
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WeighΒ 2 g agarose.β
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Add to 250 mL 1Γ TAE/TBE in 500 mL flask.β
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Microwave (1β2 min, swirl every 30 s).β
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Cool to 60Β°C, add EtBr (0.5 ΞΌg/mL), pour into tray with comb.β
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Solidify 20β30 min; run at 5β10 V/cm.β
| Concentration | Grams per 100 mL | Ideal DNA (bp) |
|---|---|---|
| 0.8% | 0.8 g | 1,000β10,000 |
| 1.0% | 1.0 g | 400β8,000 |
| 1.5% | 1.5 g | 200β3,000 |
CSIR NET Tips for Agarose Questions
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Recognize w/v units; avoid v/w mix-ups.β
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0.8% suits plasmids/PCR; memorize ranges.β
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Practice: For 50 mL 1%, use 0.5 g.β
Master this for Unit 2 (Techniques) scoring.β


