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Class 11 Biotechnology Easy Quiz

Level 42 • 46/50 questions • 40 seconds per question.

Level readiness 46/50 Questions
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डीएनए अलगाव में सही नमूना चुनना क्यों जरूरी है?

Why is choosing the right sample important in DNA isolation?

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Correct Answer

A. अच्छी मात्रा और गुणवत्ता वाला डीएनए पाने के लिएTo obtain good quantity and quality DNA

Step 1

Concept

The right sample affects DNA yield and purity. In exams link sample quality with the first step.

Step 2

Why this answer is correct

The correct answer is A. अच्छी मात्रा और गुणवत्ता वाला डीएनए पाने के लिए / To obtain good quantity and quality DNA. The right sample affects DNA yield and purity. In exams link sample quality with the first step.

Step 3

Exam Tip

सही नमूना डीएनए yield और purity को प्रभावित करता है। परीक्षा में sample quality को first step से जोड़ें।

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डीएनए extraction में sample preservation का मुख्य उद्देश्य क्या है?

What is the main purpose of sample preservation in DNA extraction?

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Correct Answer

B. डीएनए degradation को कम करनाTo reduce DNA degradation

Step 1

Concept

Preservation can reduce nuclease activity and microbial growth. This keeps DNA intact.

Step 2

Why this answer is correct

The correct answer is B. डीएनए degradation को कम करना / To reduce DNA degradation. Preservation can reduce nuclease activity and microbial growth. This keeps DNA intact.

Step 3

Exam Tip

Preservation से nucleases की activity और microbial growth कम हो सकती है। इससे डीएनए intact रहता है।

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डीएनए अलगाव में ताजा ऊतक का लाभ क्या है?

What is the benefit of fresh tissue in DNA isolation?

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C. इससे बेहतर intact DNA मिल सकता हैIt can provide better intact DNA

Step 1

Concept

Fresh tissue may have less DNA degradation. Proper storage also protects quality.

Step 2

Why this answer is correct

The correct answer is C. इससे बेहतर intact DNA मिल सकता है / It can provide better intact DNA. Fresh tissue may have less DNA degradation. Proper storage also protects quality.

Step 3

Exam Tip

ताजा ऊतक में DNA degradation कम हो सकती है। सही storage भी गुणवत्ता बचाता है।

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पुराना खराब रखा नमूना डीएनए isolation को कैसे प्रभावित कर सकता है?

How can an old poorly stored sample affect DNA isolation?

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Correct Answer

D. डीएनए टूट सकता है और yield घट सकती हैDNA can break and yield can decrease

Step 1

Concept

Poor storage can increase DNA degradation and contamination. Therefore sample handling is very important.

Step 2

Why this answer is correct

The correct answer is D. डीएनए टूट सकता है और yield घट सकती है / DNA can break and yield can decrease. Poor storage can increase DNA degradation and contamination. Therefore sample handling is very important.

Step 3

Exam Tip

खराब storage से DNA degradation और contamination बढ़ सकती है। इसलिए sample handling बहुत important है।

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डीएनए isolation में homogenization का मुख्य काम क्या है?

What is the main role of homogenization in DNA isolation?

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A. ऊतक को समान रूप से तोड़नाBreaking tissue uniformly

Step 1

Concept

Homogenization breaks tissue into smaller parts. This helps lysis buffer work better.

Step 2

Why this answer is correct

The correct answer is A. ऊतक को समान रूप से तोड़ना / Breaking tissue uniformly. Homogenization breaks tissue into smaller parts. This helps lysis buffer work better.

Step 3

Exam Tip

Homogenization ऊतक को छोटे भागों में तोड़ता है। इससे lysis buffer बेहतर काम करता है।

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पादप ऊतक को liquid nitrogen में grind करने का लाभ क्या है?

What is the benefit of grinding plant tissue in liquid nitrogen?

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Correct Answer

B. ऊतक को brittle बनाकर degradation कम करनाMaking tissue brittle and reducing degradation

Step 1

Concept

Liquid nitrogen quickly freezes tissue. This makes grinding easier and can reduce nuclease activity.

Step 2

Why this answer is correct

The correct answer is B. ऊतक को brittle बनाकर degradation कम करना / Making tissue brittle and reducing degradation. Liquid nitrogen quickly freezes tissue. This makes grinding easier and can reduce nuclease activity.

Step 3

Exam Tip

Liquid nitrogen ऊतक को जल्दी freeze कर देता है। इससे grinding आसान और nuclease activity कम हो सकती है।

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लाइसिस buffer का सबसे सही कार्य क्या है?

What is the most correct role of lysis buffer?

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Correct Answer

C. कोशिकाओं को खोलकर डीएनए मुक्त करनाOpening cells and releasing DNA

Step 1

Concept

Lysis buffer helps break cell membrane and sometimes nuclear membrane. This releases DNA.

Step 2

Why this answer is correct

The correct answer is C. कोशिकाओं को खोलकर डीएनए मुक्त करना / Opening cells and releasing DNA. Lysis buffer helps break cell membrane and sometimes nuclear membrane. This releases DNA.

Step 3

Exam Tip

Lysis buffer cell membrane और कभी nuclear membrane को तोड़ने में मदद करता है। इससे DNA बाहर आता है।

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डीएनए isolation में detergent किस structure को मुख्यतः प्रभावित करता है?

In DNA isolation which structure does detergent mainly affect?

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Correct Answer

D. lipid membrane

Step 1

Concept

Detergent disrupts lipid membranes. This can release cellular contents and DNA.

Step 2

Why this answer is correct

The correct answer is D. lipid membrane. Detergent disrupts lipid membranes. This can release cellular contents and DNA.

Step 3

Exam Tip

Detergent lipid membrane को disrupt करता है। इससे cellular contents और DNA release हो सकते हैं।

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नाभिकीय डीएनए निकालने के लिए कौन सी झिल्ली टूटनी चाहिए?

Which membrane must break to extract nuclear DNA?

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Correct Answer

A. नाभिकीय झिल्लीNuclear membrane

Step 1

Concept

In eukaryotic cells nuclear DNA remains in the nucleus. When the nuclear membrane breaks DNA enters the solution.

Step 2

Why this answer is correct

The correct answer is A. नाभिकीय झिल्ली / Nuclear membrane. In eukaryotic cells nuclear DNA remains in the nucleus. When the nuclear membrane breaks DNA enters the solution.

Step 3

Exam Tip

Eukaryotic cells में nuclear DNA nucleus में रहता है। Nuclear membrane टूटने पर DNA solution में आता है।

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बैक्टीरियल cell wall को कमजोर करने में कौन सा enzyme helpful है?

Which enzyme is helpful in weakening bacterial cell wall?

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Correct Answer

B. lysozyme

Step 1

Concept

Lysozyme weakens bacterial peptidoglycan. This makes bacterial lysis easier.

Step 2

Why this answer is correct

The correct answer is B. lysozyme. Lysozyme weakens bacterial peptidoglycan. This makes bacterial lysis easier.

Step 3

Exam Tip

Lysozyme bacterial peptidoglycan को कमजोर करता है। इससे bacterial lysis आसान होती है।

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पौधों में cell wall तोड़ने के लिए कौन सा enzyme उपयोगी हो सकता है?

Which enzyme can be useful for breaking plant cell wall?

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Correct Answer

C. cellulase

Step 1

Concept

Plant cell wall contains cellulose. Cellulase can help break cellulose.

Step 2

Why this answer is correct

The correct answer is C. cellulase. Plant cell wall contains cellulose. Cellulase can help break cellulose.

Step 3

Exam Tip

Plant cell wall में cellulose पाया जाता है। Cellulase cellulose को तोड़ने में मदद कर सकता है।

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फंगल DNA extraction में chitinase क्यों useful है?

Why is chitinase useful in fungal DNA extraction?

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D. क्योंकि fungal wall में chitin हो सकता हैBecause fungal wall may contain chitin

Step 1

Concept

Fungal cell wall may contain chitin. Chitinase helps in wall disruption.

Step 2

Why this answer is correct

The correct answer is D. क्योंकि fungal wall में chitin हो सकता है / Because fungal wall may contain chitin. Fungal cell wall may contain chitin. Chitinase helps in wall disruption.

Step 3

Exam Tip

Fungal cell wall में chitin हो सकता है। Chitinase wall disruption में मदद करता है।

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Proteinase K DNA isolation में किस प्रकार मदद करता है?

How does Proteinase K help in DNA isolation?

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A. प्रोटीन और nucleases को degrade करकेBy degrading proteins and nucleases

Step 1

Concept

Proteinase K helps reduce protein contamination and nuclease activity. This improves DNA purity and protection.

Step 2

Why this answer is correct

The correct answer is A. प्रोटीन और nucleases को degrade करके / By degrading proteins and nucleases. Proteinase K helps reduce protein contamination and nuclease activity. This improves DNA purity and protection.

Step 3

Exam Tip

Proteinase K protein contamination और nuclease activity कम करने में मदद करता है। इससे DNA purity और protection बेहतर होती है।

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RNase treatment DNA sample में किस contamination को घटाता है?

Which contamination does RNase treatment reduce in a DNA sample?

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Correct Answer

B. RNA contamination

Step 1

Concept

RNase degrades RNA. This makes the DNA sample cleaner.

Step 2

Why this answer is correct

The correct answer is B. RNA contamination. RNase degrades RNA. This makes the DNA sample cleaner.

Step 3

Exam Tip

RNase RNA को degrade करता है। इससे DNA sample अधिक साफ बनता है।

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डीएनए sample को DNase से बचाना क्यों जरूरी है?

Why is it necessary to protect a DNA sample from DNase?

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Correct Answer

C. DNase DNA को degrade कर सकता हैDNase can degrade DNA

Step 1

Concept

DNase can break DNA into smaller fragments. Therefore nuclease-free handling is important.

Step 2

Why this answer is correct

The correct answer is C. DNase DNA को degrade कर सकता है / DNase can degrade DNA. DNase can break DNA into smaller fragments. Therefore nuclease-free handling is important.

Step 3

Exam Tip

DNase DNA को छोटे fragments में तोड़ सकता है। इसलिए nuclease-free handling जरूरी है।

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EDTA डीएनए isolation में nuclease activity कैसे घटाता है?

How does EDTA reduce nuclease activity in DNA isolation?

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D. धातु ions को chelate करकेBy chelating metal ions

Step 1

Concept

Many nucleases need ions such as magnesium. EDTA binds them and reduces activity.

Step 2

Why this answer is correct

The correct answer is D. धातु ions को chelate करके / By chelating metal ions. Many nucleases need ions such as magnesium. EDTA binds them and reduces activity.

Step 3

Exam Tip

कई nucleases को magnesium जैसे ions चाहिए होते हैं। EDTA इन्हें bind कर activity घटाता है।

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Tris buffer का DNA solution में मुख्य काम क्या है?

What is the main role of Tris buffer in a DNA solution?

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Correct Answer

A. pH स्थिर रखनाMaintaining pH

Step 1

Concept

Tris helps maintain pH. Proper pH is important for DNA stability.

Step 2

Why this answer is correct

The correct answer is A. pH स्थिर रखना / Maintaining pH. Tris helps maintain pH. Proper pH is important for DNA stability.

Step 3

Exam Tip

Tris pH को स्थिर रखने में मदद करता है। उचित pH DNA stability के लिए important है।

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TE buffer में T और E किससे जुड़े हैं?

What are T and E in TE buffer linked with?

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Correct Answer

B. Tris और EDTATris and EDTA

Step 1

Concept

In TE buffer Tris maintains pH and EDTA gives protection from nucleases. Link it with storage buffer.

Step 2

Why this answer is correct

The correct answer is B. Tris और EDTA / Tris and EDTA. In TE buffer Tris maintains pH and EDTA gives protection from nucleases. Link it with storage buffer.

Step 3

Exam Tip

TE buffer में Tris pH maintain करता है और EDTA nucleases से protection देता है। इसे storage buffer से जोड़ें।

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DNA precipitation में salt किसलिए जोड़ा जाता है?

Why is salt added in DNA precipitation?

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Correct Answer

C. DNA charges को shield करनाTo shield DNA charges

Step 1

Concept

Salt shields negative charges of DNA. This helps DNA precipitate in alcohol.

Step 2

Why this answer is correct

The correct answer is C. DNA charges को shield करना / To shield DNA charges. Salt shields negative charges of DNA. This helps DNA precipitate in alcohol.

Step 3

Exam Tip

Salt DNA के negative charges को shield करता है। इससे alcohol में DNA precipitate होने में मदद मिलती है।

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Sodium acetate DNA precipitation में किस भूमिका से जुड़ा है?

Sodium acetate is linked with which role in DNA precipitation?

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Correct Answer

D. ion support for precipitation

Step 1

Concept

Sodium acetate provides ions and helps DNA precipitation. With alcohol DNA recovery can improve.

Step 2

Why this answer is correct

The correct answer is D. ion support for precipitation. Sodium acetate provides ions and helps DNA precipitation. With alcohol DNA recovery can improve.

Step 3

Exam Tip

Sodium acetate ions provide कर DNA precipitation में मदद करता है। Alcohol के साथ DNA recovery बेहतर हो सकती है।

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Ethanol या isopropanol DNA extraction में क्यों उपयोग होते हैं?

Why are ethanol or isopropanol used in DNA extraction?

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A. DNA precipitate करने के लिएTo precipitate DNA

Step 1

Concept

Alcohol reduces DNA solubility. In the presence of salt DNA can precipitate.

Step 2

Why this answer is correct

The correct answer is A. DNA precipitate करने के लिए / To precipitate DNA. Alcohol reduces DNA solubility. In the presence of salt DNA can precipitate.

Step 3

Exam Tip

Alcohol DNA की solubility घटाता है। Salt की उपस्थिति में DNA precipitate हो सकता है।

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DNA precipitation में cold alcohol क्यों पसंद किया जाता है?

Why is cold alcohol preferred in DNA precipitation?

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Correct Answer

B. DNA solubility और घटाने के लिएTo further reduce DNA solubility

Step 1

Concept

Cold alcohol can improve DNA precipitation. This can increase DNA recovery.

Step 2

Why this answer is correct

The correct answer is B. DNA solubility और घटाने के लिए / To further reduce DNA solubility. Cold alcohol can improve DNA precipitation. This can increase DNA recovery.

Step 3

Exam Tip

Cold alcohol DNA precipitation को बेहतर कर सकता है। इससे DNA recovery बढ़ सकती है।

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DNA pellet को 70 percent ethanol से wash क्यों करते हैं?

Why is a DNA pellet washed with 70 percent ethanol?

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C. salts और impurities हटाने के लिएTo remove salts and impurities

Step 1

Concept

A 70 percent ethanol wash removes salts and small impurities. The pellet is then dried properly.

Step 2

Why this answer is correct

The correct answer is C. salts और impurities हटाने के लिए / To remove salts and impurities. A 70 percent ethanol wash removes salts and small impurities. The pellet is then dried properly.

Step 3

Exam Tip

70 percent ethanol wash salts और छोटी impurities हटाता है। इसके बाद pellet को सही तरह dry किया जाता है।

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Residual ethanol DNA sample में क्यों समस्या बन सकता है?

Why can residual ethanol be a problem in a DNA sample?

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Correct Answer

D. यह PCR और enzyme reactions को inhibit कर सकता हैIt can inhibit PCR and enzyme reactions

Step 1

Concept

Remaining ethanol can inhibit downstream reactions. Therefore dry the pellet without over-drying.

Step 2

Why this answer is correct

The correct answer is D. यह PCR और enzyme reactions को inhibit कर सकता है / It can inhibit PCR and enzyme reactions. Remaining ethanol can inhibit downstream reactions. Therefore dry the pellet without over-drying.

Step 3

Exam Tip

Bacha हुआ ethanol downstream reactions को रोक सकता है। इसलिए pellet को over-dry किए बिना dry करें।

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DNA pellet को बहुत अधिक सुखाने से क्या समस्या हो सकती है?

What problem can occur when a DNA pellet is over-dried?

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A. DNA dissolve करना कठिन हो सकता हैDNA may become difficult to dissolve

Step 1

Concept

An over-dried DNA pellet dissolves slowly in buffer. Proper drying time is important.

Step 2

Why this answer is correct

The correct answer is A. DNA dissolve करना कठिन हो सकता है / DNA may become difficult to dissolve. An over-dried DNA pellet dissolves slowly in buffer. Proper drying time is important.

Step 3

Exam Tip

Over-dried DNA pellet buffer में धीरे घुलता है। उचित drying time जरूरी है।

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Silica column DNA purification में DNA कब bind करता है?

When does DNA bind in silica column DNA purification?

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Correct Answer

B. suitable salt conditions मेंIn suitable salt conditions

Step 1

Concept

In silica columns proper salt condition allows DNA binding. After washing DNA is eluted.

Step 2

Why this answer is correct

The correct answer is B. suitable salt conditions में / In suitable salt conditions. In silica columns proper salt condition allows DNA binding. After washing DNA is eluted.

Step 3

Exam Tip

Silica columns में सही salt condition DNA binding कराती है। Wash के बाद DNA elute किया जाता है।

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Column wash step का मुख्य उद्देश्य क्या है?

What is the main purpose of the column wash step?

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Correct Answer

C. bound DNA से impurities हटानाRemoving impurities from bound DNA

Step 1

Concept

The wash step removes salts and contaminants while DNA remains on the column. This makes eluted DNA clean.

Step 2

Why this answer is correct

The correct answer is C. bound DNA से impurities हटाना / Removing impurities from bound DNA. The wash step removes salts and contaminants while DNA remains on the column. This makes eluted DNA clean.

Step 3

Exam Tip

Wash step DNA को column पर रखते हुए salts और contaminants हटाता है। इससे eluted DNA साफ होता है।

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DNA elution volume कम रखने का क्या असर हो सकता है?

What can be the effect of keeping DNA elution volume low?

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A. DNA concentration बढ़ सकती हैDNA concentration can increase

Step 1

Concept

The same DNA in lower volume can give higher concentration. Too little volume can reduce recovery.

Step 2

Why this answer is correct

The correct answer is A. DNA concentration बढ़ सकती है / DNA concentration can increase. The same DNA in lower volume can give higher concentration. Too little volume can reduce recovery.

Step 3

Exam Tip

कम volume में वही DNA घुलने से concentration बढ़ सकती है। बहुत कम volume recovery घटा सकता है।

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DNA quality check में gel electrophoresis क्यों उपयोगी है?

Why is gel electrophoresis useful in DNA quality check?

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Correct Answer

B. DNA band और degradation देखने के लिएTo see DNA band and degradation

Step 1

Concept

On gel intact DNA band and degradation smear can be seen. This is an integrity check.

Step 2

Why this answer is correct

The correct answer is B. DNA band और degradation देखने के लिए / To see DNA band and degradation. On gel intact DNA band and degradation smear can be seen. This is an integrity check.

Step 3

Exam Tip

Gel पर intact DNA band और degradation smear देखे जा सकते हैं। यह integrity check है।

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DNA gel में smear किसका संकेत हो सकता है?

What can smear in a DNA gel indicate?

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Correct Answer

C. DNA degradation

Step 1

Concept

Smear can indicate broken DNA fragments. Gentle handling and nuclease protection are necessary.

Step 2

Why this answer is correct

The correct answer is C. DNA degradation. Smear can indicate broken DNA fragments. Gentle handling and nuclease protection are necessary.

Step 3

Exam Tip

Smear टूटे हुए DNA fragments का संकेत हो सकता है। Gentle handling और nuclease protection जरूरी हैं।

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Spectrophotometer DNA isolation के बाद किसलिए उपयोगी है?

Why is a spectrophotometer useful after DNA isolation?

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D. DNA concentration और purity estimate करने के लिएTo estimate DNA concentration and purity

Step 1

Concept

A spectrophotometer estimates DNA amount and purity using absorbance reading. It is useful in quality control.

Step 2

Why this answer is correct

The correct answer is D. DNA concentration और purity estimate करने के लिए / To estimate DNA concentration and purity. A spectrophotometer estimates DNA amount and purity using absorbance reading. It is useful in quality control.

Step 3

Exam Tip

Spectrophotometer absorbance reading से DNA amount और purity का अनुमान देता है। यह quality control में useful है।

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A260 by A280 ratio लगभग 1.8 किसका संकेत देता है?

An A260 by A280 ratio of about 1.8 indicates what?

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B. शुद्ध DNA का संकेतIndication of pure DNA

Step 1

Concept

For pure DNA A260 by A280 is considered about 1.8. It is useful for checking protein contamination.

Step 2

Why this answer is correct

The correct answer is B. शुद्ध DNA का संकेत / Indication of pure DNA. For pure DNA A260 by A280 is considered about 1.8. It is useful for checking protein contamination.

Step 3

Exam Tip

Pure DNA के लिए A260 by A280 लगभग 1.8 माना जाता है। यह protein contamination check में useful है।

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A260 by A230 ratio खराब हो तो कौन सी अशुद्धियाँ हो सकती हैं?

If A260 by A230 ratio is poor which impurities may be present?

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D. salt phenol या carbohydrate impuritiesSalt phenol or carbohydrate impurities

Step 1

Concept

A260 by A230 ratio can indicate impurities like salts phenol and carbohydrates. It is especially useful in plant samples.

Step 2

Why this answer is correct

The correct answer is D. salt phenol या carbohydrate impurities / Salt phenol or carbohydrate impurities. A260 by A230 ratio can indicate impurities like salts phenol and carbohydrates. It is especially useful in plant samples.

Step 3

Exam Tip

A260 by A230 ratio salts phenol और carbohydrates जैसी impurities का संकेत दे सकता है। Plant samples में यह खास useful है।

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DNA isolation के बाद PCR से पहले क्या check करना चाहिए?

What should be checked before PCR after DNA isolation?

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A. DNA purity और concentrationDNA purity and concentration

Step 1

Concept

Correct DNA amount and purity are needed for PCR template. Contaminants can inhibit amplification.

Step 2

Why this answer is correct

The correct answer is A. DNA purity और concentration / DNA purity and concentration. Correct DNA amount and purity are needed for PCR template. Contaminants can inhibit amplification.

Step 3

Exam Tip

PCR template के लिए सही DNA amount और purity जरूरी हैं। Contaminants amplification रोक सकते हैं।

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DNA sample में phenol बचने से क्या नुकसान हो सकता है?

What harm can leftover phenol cause in a DNA sample?

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B. enzyme reactions inhibit हो सकती हैंEnzyme reactions can be inhibited

Step 1

Concept

Phenol contamination can affect reactions like PCR and restriction digestion. Proper cleanup is necessary.

Step 2

Why this answer is correct

The correct answer is B. enzyme reactions inhibit हो सकती हैं / Enzyme reactions can be inhibited. Phenol contamination can affect reactions like PCR and restriction digestion. Proper cleanup is necessary.

Step 3

Exam Tip

Phenol contamination PCR और restriction digestion जैसी reactions को प्रभावित कर सकती है। Proper cleanup जरूरी है।

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DNA sample में salt carryover क्यों समस्या है?

Why is salt carryover a problem in a DNA sample?

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C. downstream enzyme reactions रोक सकता हैIt can inhibit downstream enzyme reactions

Step 1

Concept

Excess salt can inhibit PCR and enzyme digestion. Wash step helps remove salt.

Step 2

Why this answer is correct

The correct answer is C. downstream enzyme reactions रोक सकता है / It can inhibit downstream enzyme reactions. Excess salt can inhibit PCR and enzyme digestion. Wash step helps remove salt.

Step 3

Exam Tip

Excess salt PCR और enzyme digestion को inhibit कर सकता है। Wash step salt removal में मदद करता है।

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DNA sample को nuclease-free water में dissolve क्यों किया जाता है?

Why is DNA dissolved in nuclease-free water?

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D. DNA degradation से बचने के लिएTo avoid DNA degradation

Step 1

Concept

Nuclease-free water should be free from DNA-cutting enzymes. This makes DNA storage and dilution safer.

Step 2

Why this answer is correct

The correct answer is D. DNA degradation से बचने के लिए / To avoid DNA degradation. Nuclease-free water should be free from DNA-cutting enzymes. This makes DNA storage and dilution safer.

Step 3

Exam Tip

Nuclease-free water DNA-cutting enzymes से मुक्त होना चाहिए। इससे DNA storage और dilution सुरक्षित होते हैं।

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DNA aliquots बनाने का मुख्य लाभ क्या है?

What is the main benefit of making DNA aliquots?

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A. बार-बार freeze-thaw से बचनाAvoiding repeated freeze-thaw

Step 1

Concept

Aliquots avoid repeated thawing of the same tube. This preserves DNA integrity.

Step 2

Why this answer is correct

The correct answer is A. बार-बार freeze-thaw से बचना / Avoiding repeated freeze-thaw. Aliquots avoid repeated thawing of the same tube. This preserves DNA integrity.

Step 3

Exam Tip

Aliquots से same tube बार-बार thaw नहीं करनी पड़ती। इससे DNA integrity बचती है।

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DNA sample labeling क्यों आवश्यक है?

Why is DNA sample labeling necessary?

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B. sample mix-up रोकने के लिएTo prevent sample mix-up

Step 1

Concept

A label tracks sample identity and date. This is necessary for reproducibility and correct analysis.

Step 2

Why this answer is correct

The correct answer is B. sample mix-up रोकने के लिए / To prevent sample mix-up. A label tracks sample identity and date. This is necessary for reproducibility and correct analysis.

Step 3

Exam Tip

Label sample identity और date track करता है। यह reproducibility और correct analysis के लिए जरूरी है।

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DNA isolation में blank control spectrophotometer reading में क्यों उपयोग होता है?

Why is a blank control used in spectrophotometer reading for DNA isolation?

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C. buffer background subtract करने के लिएTo subtract buffer background

Step 1

Concept

The blank is the same buffer or solvent in which DNA is dissolved. This makes reading more accurate.

Step 2

Why this answer is correct

The correct answer is C. buffer background subtract करने के लिए / To subtract buffer background. The blank is the same buffer or solvent in which DNA is dissolved. This makes reading more accurate.

Step 3

Exam Tip

Blank उसी buffer या solvent से लिया जाता है जिसमें DNA घुला है। इससे reading अधिक accurate होती है।

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DNA extraction negative control किसलिए रखा जाता है?

Why is a DNA extraction negative control kept?

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D. reagent contamination check करने के लिएTo check reagent contamination

Step 1

Concept

A negative extraction control has no sample. If DNA signal appears contamination may be present.

Step 2

Why this answer is correct

The correct answer is D. reagent contamination check करने के लिए / To check reagent contamination. A negative extraction control has no sample. If DNA signal appears contamination may be present.

Step 3

Exam Tip

Negative extraction control में sample नहीं होता। DNA signal आए तो contamination हो सकती है।

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DNA extraction positive control का उद्देश्य क्या है?

What is the purpose of a DNA extraction positive control?

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A. method काम कर रही है या नहीं देखनाTo see whether the method is working

Step 1

Concept

A known sample should give DNA. This verifies the protocol and reagents.

Step 2

Why this answer is correct

The correct answer is A. method काम कर रही है या नहीं देखना / To see whether the method is working. A known sample should give DNA. This verifies the protocol and reagents.

Step 3

Exam Tip

Known sample से DNA मिलना चाहिए। इससे protocol और reagents verify होते हैं।

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DNA isolation में PPE का मुख्य उद्देश्य क्या है?

What is the main purpose of PPE in DNA isolation?

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C. sample और worker safety बनाए रखनाMaintaining sample and worker safety

Step 1

Concept

PPE reduces contamination and exposure risk. Gloves lab coat and eye protection can be useful.

Step 2

Why this answer is correct

The correct answer is C. sample और worker safety बनाए रखना / Maintaining sample and worker safety. PPE reduces contamination and exposure risk. Gloves lab coat and eye protection can be useful.

Step 3

Exam Tip

PPE contamination और exposure risk घटाता है। Gloves lab coat और eye protection उपयोगी हो सकते हैं।

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Phenol waste को कैसे dispose करना चाहिए?

How should phenol waste be disposed?

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D. approved chemical waste route सेThrough approved chemical waste route

Step 1

Concept

Phenol is a hazardous chemical. It should be disposed through chemical waste route according to safety rules.

Step 2

Why this answer is correct

The correct answer is D. approved chemical waste route से / Through approved chemical waste route. Phenol is a hazardous chemical. It should be disposed through chemical waste route according to safety rules.

Step 3

Exam Tip

Phenol hazardous chemical है। इसे safety rules के अनुसार chemical waste route से dispose करना चाहिए।

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Level 42 Isolation of DNA का सबसे अच्छा revision point क्या है?

What is the best revision point of Level 42 Isolation of DNA?

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A. sample lysis cleanup precipitation quality check याद रखेंRemember sample lysis cleanup precipitation quality check

Step 1

Concept

DNA isolation is a stepwise process. Each step affects yield purity and integrity.

Step 2

Why this answer is correct

The correct answer is A. sample lysis cleanup precipitation quality check याद रखें / Remember sample lysis cleanup precipitation quality check. DNA isolation is a stepwise process. Each step affects yield purity and integrity.

Step 3

Exam Tip

DNA isolation stepwise process है। हर step yield purity और integrity को प्रभावित करता है।

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DNA isolation का exam-safe summary क्या है?

What is the exam-safe summary of DNA isolation?

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A. cell से DNA निकालना और impurities हटानाExtracting DNA from cells and removing impurities

Step 1

Concept

DNA isolation is a basic step of recombinant DNA technology. Clean DNA is useful in PCR cloning and analysis.

Step 2

Why this answer is correct

The correct answer is A. cell से DNA निकालना और impurities हटाना / Extracting DNA from cells and removing impurities. DNA isolation is a basic step of recombinant DNA technology. Clean DNA is useful in PCR cloning and analysis.

Step 3

Exam Tip

DNA isolation recombinant DNA technology की basic step है। Clean DNA आगे PCR cloning और analysis में काम आता है।

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FAQs

Class 11 Biotechnology Quiz FAQs

How many questions are in this quiz?

This level is designed for 50 active questions. Currently 46 questions are available for the selected class and difficulty.

Is there a timer in this quiz?

Yes, the timer uses 40 seconds per question for Easy difficulty and shows the total remaining time on the page.

Can I open each question separately?

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