For an application where you require a sample of your target protein at high purity, what would be a good purification strategy? Assume that your starting point is E. coli cells in which the target protein fused to an affinity tag has been over-expressed.

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#Question id: 10336

#Part-B Specialized Branches in Biotechnology

methemoglobinemia, a disease, What will cause inside the human body?

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#Question id: 12813

#Part-A Aptitude & General Biotechnology

A took 15 sec. to cross a rectangular field diagonally walking at the rate of 52 m/min. and B took the same time to cross the same field along its sides walking at the rate of 68 m/min. The area of the field is :

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#Question id: 901

#Part-B Specialized Branches in Biotechnology

Proteins with high Tm values are generally stable at

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#Question id: 12883

#Part-A Aptitude & General Biotechnology

The volume of a cuboid is twice the volume of a cube. If the dimensions of the cuboid are 9 cm, 8 cm and 6 cm, the total surface area of the cube is :

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#Question id: 12904

#Part-A Aptitude & General Biotechnology

Match the following:

1. Southern Blotting                               i. Melting temperature of DNA strand

2. DNA microchips                                   ii.oligonucleotide matching to DNA sample

3. ASO-PCR                                                 iii.DNA hybridization to oligo arrays

4. DGGE                                                        iv. labeled probe hybridization to DNA