TLS Online TPP Program

#Question id: 2073


The phosphate transport system in bacteria imports phosphate into the cell even when the concentration of phosphate outside the cell is much lower than the cytoplasmic phosphate concentration. Phosphate import depends on a pH gradient across the membrane—more acidic outside the cell than inside the cell. In this bacterial cell, phosphate transport is an example of:

#Zoology
  1. passive diffusion

  2. facilitated diffusion

  3. active transport

  4. cotransport

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TLS Online TPP Program

#Question id: 23190

#Zoology

If we want to view live cells which microscopy can be best used for this?
1. Structured illumination microscopy
2. Phase contrast microscopy
3. Scanning electron microscopy
4. Cryoelectron microscopy
Which of the following option has correct combination?

TLS Online TPP Program

#Question id: 23190

#Life Sciences

If we want to view live cells which microscopy can be best used for this?
1. Structured illumination microscopy
2. Phase contrast microscopy
3. Scanning electron microscopy
4. Cryoelectron microscopy
Which of the following option has correct combination?

TLS Online TPP Program

#Question id: 23190

#Applied Microbiology

If we want to view live cells which microscopy can be best used for this?
1. Structured illumination microscopy
2. Phase contrast microscopy
3. Scanning electron microscopy
4. Cryoelectron microscopy
Which of the following option has correct combination?

TLS Online TPP Program

#Question id: 23193

#Zoology

When you try to image two fluorescent spots separated by 75 nm the fluorescence overlap so much that they look like one spot. Which microscopy can resolve this?

TLS Online TPP Program

#Question id: 23193

#Life Sciences

When you try to image two fluorescent spots separated by 75 nm the fluorescence overlap so much that they look like one spot. Which microscopy can resolve this?

TLS Online TPP Program

#Question id: 23193

#Applied Microbiology

When you try to image two fluorescent spots separated by 75 nm the fluorescence overlap so much that they look like one spot. Which microscopy can resolve this?