Confocal Microscopy

The principle of confocal imaging is that light is only collected from the part of the specimen which is in focus.

Out of focus regions of the sample appear black, thus eliminating all unwanted glare.

Low light levels require the use of photomultipliers.

Photon Counting Modules

Type

Effective cathode dia. mm

Cathode type

Spectral response range nm

Typical dark counts@ 20°C

Max count rate MHz

Output signal

Outline drawing

Data Sheet

P25PC

22

bialkali

280 to 630

100s-1

100

TTL

P25PC-16

22

S20

300 to 850

100s-1

100

TTL

P25USB

22

bialkali

280 to 630

100s-1

100

USB

P25USB-01

22

S20

300 to 850

100s-1

100

USB

P30PC

25

bialkali

280 to 630

100s-1

100

TTL

P30USB

25

bialkali

280 to 850

100s-1

100

USB

DM0016C

22

bialkali

280 to 630

50s-1

70

TTL

DM0087C

22

S20

300 to 850

50s-1

70

TTL

DM0089C

22

bialkali

280 to 630

50s-1

70

USB

DM0090C

22

S20

300 to 850

50s-1

70

USB

Examples of Analogue Modules

Type

Effective cathode dia. mm

Cathode type

Spectral response range nm

Amplifier bandwidth MHz

Outline drawing

Data Sheet

P30PVN

25

S20

300 to 630

-

DM0088C

22

S20

300 to 850

20

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