Skip to content

Update

Muft Shiksha™ एक 100% Free Education Portal है 🇮🇳, जिसका उद्देश्य Class 9–12 के हर विद्यार्थी तक High-Quality Education को पूरी तरह मुफ्त पहुँचाना है। 🇮🇳 हम मानते हैं कि अच्छी शिक्षा किसी student की आर्थिक स्थिति पर निर्भर नहीं होनी चाहिए। 🇮🇳 हर विद्यार्थी को वही Quality Study Material, MCQs, Quizzes, Exam Preparation, Concept-Based Learning और Bilingual Support मिलना चाहिए, जो आमतौर पर महंगी Coaching या Premium Platforms में मिलता है। Muft Shiksha™ 🇮🇳 इसी सोच के साथ बनाया गया है

RELATED QUESTIONS

Ligation

Class 11 Biotechnology के इस tag से जुड़े questions। हर question के साथ chapter, topic, level और difficulty दी गई है।

BiotechnologyWhy is cleanliness of DNA ends important before ligation after restriction cutting?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhy can cleanup be needed after alkaline phosphatase treatment?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhy is insert to vector molar ratio important?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyIf enzyme activity remains after restriction digestion what is the risk in next cloning step?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhen can destruction of a restriction site be useful in cloning verification?Class 11Processes of Recombinant DNA TechnologyLigationMedium BiotechnologyWhy is the recognition site not always restored after compatible ends ligate?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhy can blunt ends be relatively difficult to ligate?Class 11Processes of Recombinant DNA TechnologyLigationMedium BiotechnologyWhy are compatible sticky ends useful in restriction digestion?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhat is the common next step after cutting DNA?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyHow does DNA ligase make the ends produced by restriction digestion permanent?Class 11Processes of Recombinant DNA TechnologyLigationEasy BiotechnologyWhy are DNA ends purified before ligation after restriction digestion?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhy should vector ends be compatible before ligation after restriction digestion?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhen is cleanup after restriction enzyme reaction helpful?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhy is insert purification done after restriction digestion?Class 11Processes of Recombinant DNA TechnologyCutting of DNAMedium BiotechnologyHow can compatible sticky ends be produced by different enzymes?Class 11Processes of Recombinant DNA TechnologyCutting of DNAEasy BiotechnologyWhich option gives the correct cloning workflow order?Class 11Principles of BiotechnologyCloning VectorsEasy BiotechnologyWhat happens if vector and insert ends are not compatible?Class 11Processes of Recombinant DNA TechnologyLigationMedium BiotechnologyWhich option gives the correct sequence of ligase and transformation?Class 11Principles of BiotechnologyLigase EnzymesEasy BiotechnologyWhy are compatible ends important in ligase reaction?Class 11Principles of BiotechnologyLigase EnzymesEasy BiotechnologyWhat is the risk if vector is high and insert is low in ligase reaction?Class 11Principles of BiotechnologyLigase EnzymesEasy