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Class 11 Biotechnology Easy Quiz

Level 47 • 48/50 questions • 40 seconds per question.

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Recombinant DNA बनाने में DNA cutting का immediate purpose क्या है?

What is the immediate purpose of DNA cutting in making recombinant DNA?

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Correct Answer

A. insert और vector को compatible बनानाMaking insert and vector compatible

Step 1

Concept

Cutting gives insert and vector ends that can join. Ligation follows this step.

Step 2

Why this answer is correct

The correct answer is A. insert और vector को compatible बनाना / Making insert and vector compatible. Cutting gives insert and vector ends that can join. Ligation follows this step.

Step 3

Exam Tip

Cutting insert और vector को ऐसे ends देता है जो जुड़ सकते हैं। इसके बाद ligation step आता है।

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Insert release restriction digestion में क्या अर्थ रखता है?

What does insert release mean in restriction digestion?

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Correct Answer

B. desired DNA fragment को vector या source DNA से अलग करनाSeparating desired DNA fragment from vector or source DNA

Step 1

Concept

In insert release the desired fragment is cut out by restriction sites. It can be purified from gel.

Step 2

Why this answer is correct

The correct answer is B. desired DNA fragment को vector या source DNA से अलग करना / Separating desired DNA fragment from vector or source DNA. In insert release the desired fragment is cut out by restriction sites. It can be purified from gel.

Step 3

Exam Tip

Insert release में desired fragment restriction sites से cut होकर अलग होता है। इसे gel से purify किया जा सकता है।

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Vector backbone का अर्थ क्या है?

What does vector backbone mean?

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Correct Answer

C. मुख्य vector DNA जिसमें cloning elements होते हैंMain vector DNA containing cloning elements

Step 1

Concept

The vector backbone contains elements like origin marker and cloning site. The insert is joined into it.

Step 2

Why this answer is correct

The correct answer is C. मुख्य vector DNA जिसमें cloning elements होते हैं / Main vector DNA containing cloning elements. The vector backbone contains elements like origin marker and cloning site. The insert is joined into it.

Step 3

Exam Tip

Vector backbone में origin marker और cloning site जैसी elements होती हैं। Insert इसी में जोड़ा जाता है।

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Restriction digestion के बाद vector backbone और insert अलग कैसे देखे जा सकते हैं?

How can vector backbone and insert be seen separately after restriction digestion?

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Correct Answer

D. agarose gel electrophoresis सेBy agarose gel electrophoresis

Step 1

Concept

Gel electrophoresis separates fragments by size. Thus insert and backbone bands can be seen.

Step 2

Why this answer is correct

The correct answer is D. agarose gel electrophoresis से / By agarose gel electrophoresis. Gel electrophoresis separates fragments by size. Thus insert and backbone bands can be seen.

Step 3

Exam Tip

Gel electrophoresis fragments को size के आधार पर अलग करता है। इससे insert और backbone bands दिख सकते हैं।

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MCS का DNA cutting में क्या role है?

What is the role of MCS in DNA cutting?

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Correct Answer

A. कई restriction sites देनाProviding multiple restriction sites

Step 1

Concept

MCS contains many restriction sites. This allows insert cloning using suitable enzymes.

Step 2

Why this answer is correct

The correct answer is A. कई restriction sites देना / Providing multiple restriction sites. MCS contains many restriction sites. This allows insert cloning using suitable enzymes.

Step 3

Exam Tip

MCS में कई restriction sites होती हैं। इससे suitable enzyme चुनकर insert cloning की जा सकती है।

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Multiple restriction sites वाले vector का लाभ क्या है?

What is the benefit of a vector with multiple restriction sites?

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Correct Answer

C. cloning enzyme choice में flexibility देता हैIt gives flexibility in choosing cloning enzymes

Step 1

Concept

Multiple sites allow cloning with different enzymes. This is a major benefit of MCS.

Step 2

Why this answer is correct

The correct answer is C. cloning enzyme choice में flexibility देता है / It gives flexibility in choosing cloning enzymes. Multiple sites allow cloning with different enzymes. This is a major benefit of MCS.

Step 3

Exam Tip

Multiple sites अलग-अलग enzymes से cloning की सुविधा देते हैं। यह MCS का बड़ा लाभ है।

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Restriction site insert के अंदर भी हो तो क्या समस्या हो सकती है?

What problem can occur if a restriction site is also inside the insert?

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Correct Answer

D. insert unwanted fragments में कट सकता हैInsert can cut into unwanted fragments

Step 1

Concept

If the chosen enzyme cuts inside the insert the desired gene can break. Check sequence before enzyme choice.

Step 2

Why this answer is correct

The correct answer is D. insert unwanted fragments में कट सकता है / Insert can cut into unwanted fragments. If the chosen enzyme cuts inside the insert the desired gene can break. Check sequence before enzyme choice.

Step 3

Exam Tip

अगर chosen enzyme insert के अंदर cut करे तो desired gene टूट सकता है। Enzyme choice से पहले sequence check करें।

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Enzyme choice से पहले insert sequence क्यों check की जाती है?

Why is insert sequence checked before enzyme choice?

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A. internal restriction sites से बचने के लिएTo avoid internal restriction sites

Step 1

Concept

If the chosen enzyme site is inside the insert the insert can break. Therefore sequence analysis is needed in cloning planning.

Step 2

Why this answer is correct

The correct answer is A. internal restriction sites से बचने के लिए / To avoid internal restriction sites. If the chosen enzyme site is inside the insert the insert can break. Therefore sequence analysis is needed in cloning planning.

Step 3

Exam Tip

Insert में chosen enzyme site हो तो insert टूट सकता है। इसलिए sequence analysis cloning planning में जरूरी है।

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Restriction digestion से orientation check कैसे हो सकती है?

How can restriction digestion help check orientation?

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Correct Answer

B. different band sizes pattern सेBy different band size pattern

Step 1

Concept

Depending on insert orientation distances between restriction sites can change. Digest pattern can indicate orientation.

Step 2

Why this answer is correct

The correct answer is B. different band sizes pattern से / By different band size pattern. Depending on insert orientation distances between restriction sites can change. Digest pattern can indicate orientation.

Step 3

Exam Tip

Insert orientation के अनुसार restriction sites की distance बदल सकती है। Digest pattern से orientation का संकेत मिलता है।

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Diagnostic digest में single enzyme use कब useful हो सकता है?

When can using a single enzyme be useful in diagnostic digest?

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C. plasmid linearization या simple size check के लिएFor plasmid linearization or simple size check

Step 1

Concept

A single cut can convert plasmid into linear form. This can help check approximate plasmid size.

Step 2

Why this answer is correct

The correct answer is C. plasmid linearization या simple size check के लिए / For plasmid linearization or simple size check. A single cut can convert plasmid into linear form. This can help check approximate plasmid size.

Step 3

Exam Tip

Single cut plasmid को linear form में बदल सकता है। इससे approximate plasmid size check हो सकता है।

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Diagnostic digest में two-enzyme cut का लाभ क्या है?

What is the benefit of a two-enzyme cut in diagnostic digest?

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D. insert size या orientation बेहतर check करनाBetter checking insert size or orientation

Step 1

Concept

Two enzymes give an expected fragment pattern. This can make clone verification more informative.

Step 2

Why this answer is correct

The correct answer is D. insert size या orientation बेहतर check करना / Better checking insert size or orientation. Two enzymes give an expected fragment pattern. This can make clone verification more informative.

Step 3

Exam Tip

Two enzymes expected fragment pattern देते हैं। इससे clone verification अधिक informative हो सकता है।

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Restriction digest में plasmid uncut band क्यों दिखाई दे सकता है?

Why can an uncut plasmid band appear in restriction digest?

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Correct Answer

A. incomplete digestion के कारणDue to incomplete digestion

Step 1

Concept

In incomplete digestion some plasmid can remain uncut. Uncut and cut forms can appear together on gel.

Step 2

Why this answer is correct

The correct answer is A. incomplete digestion के कारण / Due to incomplete digestion. In incomplete digestion some plasmid can remain uncut. Uncut and cut forms can appear together on gel.

Step 3

Exam Tip

Incomplete digestion में कुछ plasmid uncut रह सकता है। Gel पर uncut और cut forms साथ दिख सकते हैं।

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Restriction digest में smear दिखना किसका संकेत हो सकता है?

What can smear in a restriction digest indicate?

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B. degraded DNA या nonspecific cuttingDegraded DNA or nonspecific cutting

Step 1

Concept

A smear can show DNA degradation or a problem like star activity. Check reaction conditions.

Step 2

Why this answer is correct

The correct answer is B. degraded DNA या nonspecific cutting / Degraded DNA or nonspecific cutting. A smear can show DNA degradation or a problem like star activity. Check reaction conditions.

Step 3

Exam Tip

Smear DNA degradation या star activity जैसी समस्या दिखा सकता है। Reaction conditions check करें।

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Gel पर expected insert band नहीं दिखे तो क्या संभव है?

What is possible if expected insert band is not seen on gel?

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A. insert absent या digestion failed हो सकता हैInsert may be absent or digestion failed

Step 1

Concept

Absence of expected band can indicate wrong clone partial digestion or low DNA amount. Confirm with controls.

Step 2

Why this answer is correct

The correct answer is A. insert absent या digestion failed हो सकता है / Insert may be absent or digestion failed. Absence of expected band can indicate wrong clone partial digestion or low DNA amount. Confirm with controls.

Step 3

Exam Tip

Expected band न होना wrong clone partial digestion या low DNA amount का संकेत हो सकता है। Controls से confirm करें।

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Restriction digestion के बाद band बहुत faint हो तो क्या कारण हो सकता है?

What can cause a very faint band after restriction digestion?

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Correct Answer

B. कम DNA amountLow DNA amount

Step 1

Concept

Low DNA loading gives faint bands. Check DNA concentration and loading amount.

Step 2

Why this answer is correct

The correct answer is B. कम DNA amount / Low DNA amount. Low DNA loading gives faint bands. Check DNA concentration and loading amount.

Step 3

Exam Tip

Low DNA loading से faint bands दिखते हैं। DNA concentration और loading amount check करें।

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Restriction digest के बाद बहुत bright smear क्या बताता है?

What can a very bright smear after restriction digest show?

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Correct Answer

C. overloaded DNA या degradationOverloaded DNA or degradation

Step 1

Concept

Too much DNA loading or degraded DNA can give a smear. Check gel loading and DNA quality.

Step 2

Why this answer is correct

The correct answer is C. overloaded DNA या degradation / Overloaded DNA or degradation. Too much DNA loading or degraded DNA can give a smear. Check gel loading and DNA quality.

Step 3

Exam Tip

बहुत ज्यादा DNA loading या degraded DNA smear दे सकता है। Gel loading और DNA quality check करें।

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Restriction digest result में ladder गलत चुनने से क्या समस्या होगी?

What problem occurs if the wrong ladder is chosen for restriction digest result?

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Correct Answer

D. fragment size estimate गलत हो सकता हैFragment size estimate can be wrong

Step 1

Concept

The ladder should match the expected fragment range. Wrong ladder confuses size interpretation.

Step 2

Why this answer is correct

The correct answer is D. fragment size estimate गलत हो सकता है / Fragment size estimate can be wrong. The ladder should match the expected fragment range. Wrong ladder confuses size interpretation.

Step 3

Exam Tip

Ladder expected fragment range से match होनी चाहिए। गलत ladder size interpretation को confuse करती है।

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RFLP में restriction enzyme क्यों जरूरी है?

Why is restriction enzyme necessary in RFLP?

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B. DNA को specific fragments में काटने के लिएTo cut DNA into specific fragments

Step 1

Concept

Restriction enzyme cuts DNA into site-specific fragments. Fragment pattern is used in variation analysis.

Step 2

Why this answer is correct

The correct answer is B. DNA को specific fragments में काटने के लिए / To cut DNA into specific fragments. Restriction enzyme cuts DNA into site-specific fragments. Fragment pattern is used in variation analysis.

Step 3

Exam Tip

Restriction enzyme DNA को site-specific fragments में काटता है। Fragment pattern variation analysis में use होता है।

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Restriction digestion cloning में false result कब दे सकता है?

When can restriction digestion give a false result in cloning?

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C. अगर partial digestion या wrong enzyme होIf partial digestion or wrong enzyme occurs

Step 1

Concept

Partial digestion or wrong enzyme can give misleading band patterns. Confirm with controls and sequencing.

Step 2

Why this answer is correct

The correct answer is C. अगर partial digestion या wrong enzyme हो / If partial digestion or wrong enzyme occurs. Partial digestion or wrong enzyme can give misleading band patterns. Confirm with controls and sequencing.

Step 3

Exam Tip

Partial digestion या wrong enzyme misleading band pattern दे सकते हैं। Controls और sequencing से पुष्टि करें।

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Wrong enzyme use करने से cloning में क्या हो सकता है?

What can happen in cloning if the wrong enzyme is used?

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A. desired compatible ends नहीं बनेंगेDesired compatible ends will not form

Step 1

Concept

The wrong enzyme can cut vector or insert at the wrong place. This can cause cloning failure.

Step 2

Why this answer is correct

The correct answer is A. desired compatible ends नहीं बनेंगे / Desired compatible ends will not form. The wrong enzyme can cut vector or insert at the wrong place. This can cause cloning failure.

Step 3

Exam Tip

Wrong enzyme vector या insert को गलत जगह काट सकता है। इससे cloning fail हो सकती है।

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Restriction digest setup में master mix कब useful हो सकता है?

When can a master mix be useful in restriction digest setup?

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A. multiple similar reactions में pipetting variation घटाने के लिएTo reduce pipetting variation in multiple similar reactions

Step 1

Concept

A master mix keeps common components same. This improves reproducibility and pipetting accuracy.

Step 2

Why this answer is correct

The correct answer is A. multiple similar reactions में pipetting variation घटाने के लिए / To reduce pipetting variation in multiple similar reactions. A master mix keeps common components same. This improves reproducibility and pipetting accuracy.

Step 3

Exam Tip

Master mix common components को समान रखता है। इससे reproducibility और pipetting accuracy बेहतर होती है।

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Reaction setup में labels क्यों जरूरी हैं?

Why are labels important in reaction setup?

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

Step 1

Concept

Clear labels prevent wrong enzyme or wrong sample mix-up. This is necessary for reliable results.

Step 2

Why this answer is correct

The correct answer is C. sample mix-up रोकने के लिए / To prevent sample mix-up. Clear labels prevent wrong enzyme or wrong sample mix-up. This is necessary for reliable results.

Step 3

Exam Tip

Clear labels wrong enzyme या wrong sample mix-up से बचाते हैं। यह reliable result के लिए जरूरी है।

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Restriction enzyme notebook में क्या record करना useful है?

What is useful to record in a restriction enzyme notebook?

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A. enzyme name buffer temperature और resultEnzyme name buffer temperature and result

Step 1

Concept

Records help troubleshooting and repeat experiments. Recording enzyme conditions is important.

Step 2

Why this answer is correct

The correct answer is A. enzyme name buffer temperature और result / Enzyme name buffer temperature and result. Records help troubleshooting and repeat experiments. Recording enzyme conditions is important.

Step 3

Exam Tip

Records troubleshooting और repeat experiments में मदद करते हैं। Enzyme conditions का record important है।

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Restriction digestion में biosafety का मुख्य संबंध किससे है?

What is biosafety mainly related to in restriction digestion?

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B. sample और chemical safe handling सेSafe handling of sample and chemicals

Step 1

Concept

DNA samples and reagents should be handled safely. Follow PPE and disposal rules.

Step 2

Why this answer is correct

The correct answer is B. sample और chemical safe handling से / Safe handling of sample and chemicals. DNA samples and reagents should be handled safely. Follow PPE and disposal rules.

Step 3

Exam Tip

DNA samples और reagents को safe तरीके से handle करना चाहिए। PPE और disposal rules follow करें।

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Ethidium bromide जैसे DNA stain के साथ क्या जरूरी है?

What is necessary while using DNA stains like ethidium bromide?

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A. safe handling और proper disposalSafe handling and proper disposal

Step 1

Concept

Some DNA stains can be hazardous. Gloves and approved waste disposal are necessary.

Step 2

Why this answer is correct

The correct answer is A. safe handling और proper disposal / Safe handling and proper disposal. Some DNA stains can be hazardous. Gloves and approved waste disposal are necessary.

Step 3

Exam Tip

कुछ DNA stains hazardous हो सकते हैं। Gloves और approved waste disposal जरूरी हैं।

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Restriction digestion के बाद gel documentation क्यों की जाती है?

Why is gel documentation done after restriction digestion?

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Correct Answer

A. band pattern record करने के लिएTo record band pattern

Step 1

Concept

A gel image records the band pattern. It is useful for clone verification and lab notebook.

Step 2

Why this answer is correct

The correct answer is A. band pattern record करने के लिए / To record band pattern. A gel image records the band pattern. It is useful for clone verification and lab notebook.

Step 3

Exam Tip

Gel image band pattern का record देती है। यह clone verification और lab notebook के लिए उपयोगी है।

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Restriction digestion में reproducibility कैसे बढ़ती है?

How is reproducibility increased in restriction digestion?

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A. standard protocol और accurate records सेBy standard protocol and accurate records

Step 1

Concept

Standard conditions and records help obtain similar results. This increases scientific reliability.

Step 2

Why this answer is correct

The correct answer is A. standard protocol और accurate records से / By standard protocol and accurate records. Standard conditions and records help obtain similar results. This increases scientific reliability.

Step 3

Exam Tip

Standard conditions और records same result पाने में मदद करते हैं। यह scientific reliability बढ़ाता है।

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Restriction digestion result को sequencing से क्यों confirm किया जा सकता है?

Why can a restriction digestion result be confirmed by sequencing?

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A. sequencing exact base order बताती हैSequencing tells the exact base order

Step 1

Concept

Restriction digest gives size pattern but not exact sequence. Sequencing can give final confirmation.

Step 2

Why this answer is correct

The correct answer is A. sequencing exact base order बताती है / Sequencing tells the exact base order. Restriction digest gives size pattern but not exact sequence. Sequencing can give final confirmation.

Step 3

Exam Tip

Restriction digest size pattern देता है पर exact sequence नहीं। Sequencing final confirmation दे सकती है।

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Restriction digestion और PCR में मुख्य अंतर क्या है?

What is the main difference between restriction digestion and PCR?

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A. restriction digestion DNA काटता है और PCR DNA amplify करता हैRestriction digestion cuts DNA and PCR amplifies DNA

Step 1

Concept

Restriction enzyme makes DNA fragments. PCR makes copies of a specific DNA region.

Step 2

Why this answer is correct

The correct answer is A. restriction digestion DNA काटता है और PCR DNA amplify करता है / Restriction digestion cuts DNA and PCR amplifies DNA. Restriction enzyme makes DNA fragments. PCR makes copies of a specific DNA region.

Step 3

Exam Tip

Restriction enzyme DNA fragments बनाता है। PCR specific DNA region की copies बनाता है।

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Restriction enzyme और exonuclease में basic अंतर क्या है?

What is the basic difference between restriction enzyme and exonuclease?

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A. restriction enzyme specific internal sites काटता है और exonuclease ends से हटाता हैRestriction enzyme cuts specific internal sites and exonuclease removes from ends

Step 1

Concept

Restriction endonucleases cut specific internal sites in DNA. Exonucleases remove nucleotides from ends.

Step 2

Why this answer is correct

The correct answer is A. restriction enzyme specific internal sites काटता है और exonuclease ends से हटाता है / Restriction enzyme cuts specific internal sites and exonuclease removes from ends. Restriction endonucleases cut specific internal sites in DNA. Exonucleases remove nucleotides from ends.

Step 3

Exam Tip

Restriction endonucleases DNA के अंदर specific sites काटते हैं। Exonucleases ends से nucleotides हटाते हैं।

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Endonuclease शब्द का अर्थ क्या है?

What does the term endonuclease mean?

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A. nucleic acid के अंदर cut करने वाला enzymeEnzyme that cuts inside nucleic acid

Step 1

Concept

An endonuclease cuts phosphodiester bonds within a nucleic acid chain. Restriction enzymes belong to this group.

Step 2

Why this answer is correct

The correct answer is A. nucleic acid के अंदर cut करने वाला enzyme / Enzyme that cuts inside nucleic acid. An endonuclease cuts phosphodiester bonds within a nucleic acid chain. Restriction enzymes belong to this group.

Step 3

Exam Tip

Endonuclease nucleic acid chain के भीतर phosphodiester bonds काटता है। Restriction enzymes इसी group में आते हैं।

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Restriction enzymes को किस biological role से खोजा गया था?

Restriction enzymes were discovered in relation to which biological role?

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A. bacterial defense against foreign DNA

Step 1

Concept

Bacteria can cut foreign DNA using restriction enzymes. This is a natural defense mechanism.

Step 2

Why this answer is correct

The correct answer is A. bacterial defense against foreign DNA. Bacteria can cut foreign DNA using restriction enzymes. This is a natural defense mechanism.

Step 3

Exam Tip

Bacteria restriction enzymes से foreign DNA को काट सकते हैं। यह natural defense mechanism है।

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Host DNA methylation का natural purpose क्या हो सकता है?

What can be the natural purpose of host DNA methylation?

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A. host DNA को own restriction enzyme से बचानाProtecting host DNA from its own restriction enzyme

Step 1

Concept

When host DNA is methylated the restriction enzyme does not cut it. Foreign unmethylated DNA can be cut.

Step 2

Why this answer is correct

The correct answer is A. host DNA को own restriction enzyme से बचाना / Protecting host DNA from its own restriction enzyme. When host DNA is methylated the restriction enzyme does not cut it. Foreign unmethylated DNA can be cut.

Step 3

Exam Tip

Host DNA methylated होने पर restriction enzyme उसे नहीं काटता। Foreign unmethylated DNA काटा जा सकता है।

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Restriction enzyme name EcoRI में R किससे संबंधित है?

In the restriction enzyme name EcoRI what does R relate to?

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A. strain designation

Step 1

Concept

The name EcoRI is related to organism strain and order of discovery. Such naming conventions can be asked in exams.

Step 2

Why this answer is correct

The correct answer is A. strain designation. The name EcoRI is related to organism strain and order of discovery. Such naming conventions can be asked in exams.

Step 3

Exam Tip

EcoRI नाम organism strain और order of discovery से जुड़ा है। ऐसे naming conventions exam में पूछे जा सकते हैं।

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Restriction enzyme नाम में Roman numeral क्या बताता है?

What does the Roman numeral in a restriction enzyme name indicate?

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A. discovery order in that strain

Step 1

Concept

In EcoRI I shows the first identified enzyme. The Roman numeral indicates discovery order.

Step 2

Why this answer is correct

The correct answer is A. discovery order in that strain. In EcoRI I shows the first identified enzyme. The Roman numeral indicates discovery order.

Step 3

Exam Tip

EcoRI में I first identified enzyme को दिखाता है। Roman numeral discovery order बताता है।

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Restriction enzyme naming में species source क्यों important है?

Why is species source important in restriction enzyme naming?

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A. enzyme के origin को बताने के लिएTo indicate the origin of enzyme

Step 1

Concept

Restriction enzyme names are often derived from organism source. This makes naming systematic.

Step 2

Why this answer is correct

The correct answer is A. enzyme के origin को बताने के लिए / To indicate the origin of enzyme. Restriction enzyme names are often derived from organism source. This makes naming systematic.

Step 3

Exam Tip

Restriction enzyme names often organism source से बनते हैं। यह naming system को systematic बनाता है।

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Restriction digestion के बाद ligation से पहले ends को purify क्यों किया जाता है?

Why are ends purified before ligation after restriction digestion?

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A. enzyme buffer और small fragments हटाने के लिएTo remove enzyme buffer and small fragments

Step 1

Concept

Purification can reduce ligation inhibitors. Clean compatible ends give better ligation.

Step 2

Why this answer is correct

The correct answer is A. enzyme buffer और small fragments हटाने के लिए / To remove enzyme buffer and small fragments. Purification can reduce ligation inhibitors. Clean compatible ends give better ligation.

Step 3

Exam Tip

Purification ligation inhibitors को कम कर सकती है। Clean compatible ends better ligation देते हैं।

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Restriction digestion में cut fragment और vector ratio क्यों important है?

Why is cut fragment and vector ratio important in restriction digestion based cloning?

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A. ligation efficiency को प्रभावित करता हैIt affects ligation efficiency

Step 1

Concept

Suitable amounts of insert and vector help ligation success. Wrong ratio can give empty vector or low clones.

Step 2

Why this answer is correct

The correct answer is A. ligation efficiency को प्रभावित करता है / It affects ligation efficiency. Suitable amounts of insert and vector help ligation success. Wrong ratio can give empty vector or low clones.

Step 3

Exam Tip

Insert और vector की suitable मात्रा ligation success में मदद करती है। गलत ratio empty vector या low clones दे सकता है।

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Blunt end ligation sticky end ligation से कठिन क्यों हो सकती है?

Why can blunt end ligation be harder than sticky end ligation?

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A. blunt ends में complementary overhang नहीं होताBlunt ends lack complementary overhang

Step 1

Concept

Sticky ends come together by complementary pairing. Blunt ends do not have this help.

Step 2

Why this answer is correct

The correct answer is A. blunt ends में complementary overhang नहीं होता / Blunt ends lack complementary overhang. Sticky ends come together by complementary pairing. Blunt ends do not have this help.

Step 3

Exam Tip

Sticky ends complementary pairing से पास आते हैं। Blunt ends में यह सहायता नहीं होती।

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Sticky ends को cohesive ends क्यों कहा जाता है?

Why are sticky ends called cohesive ends?

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A. वे complementary bases से आपस में चिपक सकते हैंThey can stick together by complementary bases

Step 1

Concept

Sticky ends can anneal because of complementary overhangs. Therefore they are also called cohesive ends.

Step 2

Why this answer is correct

The correct answer is A. वे complementary bases से आपस में चिपक सकते हैं / They can stick together by complementary bases. Sticky ends can anneal because of complementary overhangs. Therefore they are also called cohesive ends.

Step 3

Exam Tip

Sticky ends complementary overhangs के कारण anneal कर सकते हैं। इसलिए इन्हें cohesive ends भी कहते हैं।

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Restriction enzyme digestion में annealing किससे जुड़ा है?

Annealing in restriction enzyme digestion is linked with what?

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A. complementary sticky ends का pairingPairing of complementary sticky ends

Step 1

Concept

Complementary sticky ends can temporarily base pair. Ligase later forms the bond.

Step 2

Why this answer is correct

The correct answer is A. complementary sticky ends का pairing / Pairing of complementary sticky ends. Complementary sticky ends can temporarily base pair. Ligase later forms the bond.

Step 3

Exam Tip

Complementary sticky ends temporary base pairing कर सकते हैं। Ligase बाद में bond बनाता है।

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Restriction digestion से बने ends को ligase स्थायी कैसे बनाता है?

How does ligase make ends produced by restriction digestion permanent?

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A. phosphodiester bonds बनाकरBy forming phosphodiester bonds

Step 1

Concept

Ligase forms phosphodiester bonds in the DNA backbone. This makes recombinant DNA stable.

Step 2

Why this answer is correct

The correct answer is A. phosphodiester bonds बनाकर / By forming phosphodiester bonds. Ligase forms phosphodiester bonds in the DNA backbone. This makes recombinant DNA stable.

Step 3

Exam Tip

Ligase DNA backbone में phosphodiester bonds बनाता है। इससे recombinant DNA स्थायी बनता है।

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Cutting of DNA के बाद अगला सामान्य step कौन सा है?

What is the common next step after cutting DNA?

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A. DNA ligation

Step 1

Concept

After cutting compatible DNA fragments are joined by ligase. This is the next step of recombinant DNA formation.

Step 2

Why this answer is correct

The correct answer is A. DNA ligation. After cutting compatible DNA fragments are joined by ligase. This is the next step of recombinant DNA formation.

Step 3

Exam Tip

Cutting के बाद compatible DNA fragments को ligase से जोड़ा जाता है। यह recombinant DNA formation का next step है।

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Restriction digestion की failure troubleshooting में सबसे पहले क्या check कर सकते हैं?

What can be checked first while troubleshooting restriction digestion failure?

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A. enzyme buffer temperature और DNA qualityEnzyme buffer temperature and DNA quality

Step 1

Concept

Digestion failure can often relate to enzyme condition DNA purity or temperature. Check controls too.

Step 2

Why this answer is correct

The correct answer is A. enzyme buffer temperature और DNA quality / Enzyme buffer temperature and DNA quality. Digestion failure can often relate to enzyme condition DNA purity or temperature. Check controls too.

Step 3

Exam Tip

Digestion failure अक्सर enzyme condition DNA purity या temperature से जुड़ा हो सकता है। Controls भी check करें।

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Restriction digestion report में क्या लिखना चाहिए?

What should be written in a restriction digestion report?

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A. enzyme names expected bands observed bands और conditionsEnzyme names expected bands observed bands and conditions

Step 1

Concept

The report compares expected and observed patterns. This helps result interpretation and repeat work.

Step 2

Why this answer is correct

The correct answer is A. enzyme names expected bands observed bands और conditions / Enzyme names expected bands observed bands and conditions. The report compares expected and observed patterns. This helps result interpretation and repeat work.

Step 3

Exam Tip

Report में expected और observed pattern compare किया जाता है। इससे result interpretation और repeat work आसान होता है।

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Restriction digestion में expected और observed bands compare क्यों करते हैं?

Why are expected and observed bands compared in restriction digestion?

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A. construct या digestion सही है या नहीं जानने के लिएTo know whether construct or digestion is correct

Step 1

Concept

Expected pattern comes from the map and observed pattern comes from gel. Comparison helps clone verification.

Step 2

Why this answer is correct

The correct answer is A. construct या digestion सही है या नहीं जानने के लिए / To know whether construct or digestion is correct. Expected pattern comes from the map and observed pattern comes from gel. Comparison helps clone verification.

Step 3

Exam Tip

Expected pattern map से आता है और observed pattern gel से मिलता है। Comparison clone verification में मदद करता है।

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Level 47 का best exam revision point क्या है?

What is the best exam revision point of Level 47?

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A. enzyme choice restriction map diagnostic digest और gel interpretation याद रखेंRemember enzyme choice restriction map diagnostic digest and gel interpretation

Step 1

Concept

Cutting of DNA is important in both cloning planning and clone verification. Compare band pattern with the map.

Step 2

Why this answer is correct

The correct answer is A. enzyme choice restriction map diagnostic digest और gel interpretation याद रखें / Remember enzyme choice restriction map diagnostic digest and gel interpretation. Cutting of DNA is important in both cloning planning and clone verification. Compare band pattern with the map.

Step 3

Exam Tip

Cutting of DNA cloning planning और clone verification दोनों में important है। Band pattern को map से compare करें।

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Cutting of DNA level 47 का final summary क्या है?

What is the final summary of Cutting of DNA level 47?

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A. सही restriction enzyme से DNA काटकर compatible fragments बनते हैं और gel से verify होते हैंCorrect restriction enzyme cuts DNA to make compatible fragments and they are verified by gel

Step 1

Concept

Restriction digestion is a key step in cloning and verification. Correct enzyme condition controls and gel interpretation are necessary.

Step 2

Why this answer is correct

The correct answer is A. सही restriction enzyme से DNA काटकर compatible fragments बनते हैं और gel से verify होते हैं / Correct restriction enzyme cuts DNA to make compatible fragments and they are verified by gel. Restriction digestion is a key step in cloning and verification. Correct enzyme condition controls and gel interpretation are necessary.

Step 3

Exam Tip

Restriction digestion cloning और verification की key step है। सही enzyme condition controls और gel interpretation जरूरी हैं।

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FAQs

Class 11 Biotechnology Quiz FAQs

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This level is designed for 50 active questions. Currently 48 questions are available for the selected class and difficulty.

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