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10 short instructions, Preparation, Methods – Eppendorf BioPhotometer User Manual

Page 39: Cuvettes

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81

10 Short instructions

Preparation

The BioPhotometer is ready to measure immediately after being switched on.

Methods

dsDNA ssDNA RNA Oligo

– Direct measurement of the nucleic acids at 260 nm.
– Ratios A

260

/A

280

and A

260

/A

230

.

– Optional correction of absorbance values via A

320.

– Measurement using quartz-glass cuvette or UVette

®

from Eppendorf.

OD 600

– Direct measurement of the density of bacteria suspensions
at 600 nm (turbidity measurement).
– Measurement using glass cuvette or plastic cuvette.

Protein

– Direct measurement of protein at 280 nm.
– Direct measurement of the absorbance, or calculation via factor,
standard or Warburg formula.
– Optional correction of absorbance values via A

320.

– Measurement using quartz-glass cuvette or UVette

®

from Eppendorf.

Bradford Lowry BCA
Bradford micro Lowry micro BCA micro

– Measurement of protein using Bradford-, Lowry- or BCA reagent.
– Direct measurement of the absorbance,
or calculation via factor or calibration
(single-point calibration, linear regression or non-linear regression).
– Number and nominal values of the calibrators are programmable.
– The protein methods are also available on a micro-scale
(Press the Method key twice).
– Measurement using glass cuvette or plastic cuvette.

8

ssDNA

7

dsDNA

9

RNA

6

Oligo

5

OD 600

4

Protein

1

Bradford

2

Lowry

3

BCA

7

dsDNA

8

ssDNA

9

RNA

6

Oligo

5

OD 600

4

Protein

1

Bradford

2

Lowry

3

BCA

Cuvettes

Min. overall height

Min. filling level

Min. volume

36 mm

Light path
Max. height of base

10 mm

8.5 mm
7 mm
0 mm

70

µL

400

µL

1000

µL

300

µL

Semi-micro

Macro

Suction

Basic area
12.5 mm x 12.5 mm

Ultra-micro

UVette

®

50

µL

10_Kurz_e.fm Seite 81 Montag, 20. Februar 2006 11:33 Uhr