Owner's manual
Table Of Contents
- 1 Overview
- 2 Safety instructions
- 3 Commissioning
- 4 Operation
- 4.1 Switching on or off the photometer
- 4.2 General operating principles
- 4.3 Photometer settings and system administration
- 4.4 Zero adjustment
- 4.5 Measuring in Concentration mode
- 4.5.1 Measuring cell tests with barcode
- 4.5.2 Measuring reagent tests with AutoSelector
- 4.5.3 Measuring reagent-free tests and user-defined methods
- 4.5.4 Exceeding the upper or lower limits of the measuring range
- 4.5.5 Selecting a method manually
- 4.5.6 Settings for Concentration mode
- 4.5.7 Measuring diluted samples
- 4.5.8 Sample blank value
- 4.5.9 Reagent blank value
- 4.5.10 Automatic Turbidity correction
- 4.5.11 Programming / modifying user-defined methods
- 4.5.12 The IQ LabLink procedure
- 4.6 Measuring the Absorbance / % Transmission
- 4.7 Multi wavelengths methods
- 4.8 Spectrum
- 4.9 Kinetics
- 4.10 Timer
- 4.11 Memory
- 4.11.1 Overview
- 4.11.2 Instructions on using USB memory devices
- 4.11.3 Measurement datasets
- 4.11.4 Saving measurement datasets manually
- 4.11.5 Saving measurement datasets automatically
- 4.11.6 Displaying measurement data memory
- 4.11.7 Filtering measurement datasets
- 4.11.8 Inverting filters
- 4.11.9 Erasing stored measurement datasets
- 4.12 Copying files
- 4.13 Transmitting data
- 4.14 Analytical quality assurance (AQA)
- 4.15 User management
- 4.16 Reset
- 4.17 Photometer information ([Info])
- 4.18 Lamp counter
- 4.19 Software and methods update
- 5 Maintenance and cleaning
- 6 What to do if ...
- 7 Technical data
- 8 Accessories and options
- Appendix
photoLab
®
6100 VIS Operation
75
ba75847e01 08/2009
3 Page 2 of 6:
Add another wavelength with
[Add].
Delete the last wavelength with
[Delete].
4 Using [Next], accept all entries on
the page and switch to the next
page.
5 Page 3 of 6:
Enter the coefficients for the basic
equation (more detailed
information of the basic equation,
see section 4.7.1).
6 Using [Next], accept all entries on
the page and switch to the next
page.
7 Page 4 of 6:
Enter the coefficients for the basic
equation (more detailed
information of the basic equation,
see section 4.7.1).
8 Using [Next], accept all entries on
the page and switch to the next
page.
9 Page 5 of 6:
The data is displayed once again
as a summary.
Using [Back], you can correct
wrong data on the previous pages.
Using [Next], accept all entries on
the page and switch to the next
page.
The method is programmed and
selected.
Edit method (2 of 6)
04/16/07 9:52
Wavelength 1 280 nm
Wavelength 2 260 nm
Back Add Delete D Next
Edit method (3 of 6)
04/16/07 9:52
a0 + a1 * A1 + a2 * A2 + ... + a10 * A10
R=
b0 + b1 * A1 + b2 * A2 + ... + b10 * A10
a0 0.000 a6 0.000
a1 1.550 a7 0.000
a2 -0.757 a8 0.000
a3 0.000 a9 0.000
a4 0.000 a10 0.000
a5
Back Next
Edit method (4 of 6)
04/16/07 9:52
a0 + a1 * A1 + a2 * A2 + ... + a10 * A10
R=
b0 + b1 * A1 + b2 * A2 + ... + b10 * A10
b0 1.000 b6 0.000
b1 0.000 b7 0.000
b2 0.000 b8 0.000
b3 0.000 b9 0.000
b4 0.000 b10 0.000
b5
Back Next
Edit method (5 of 6)
04/16/07 9:52
Number: 2002
Name: PROT
Version: 1.0
Citation form: Protein
Unit: mg/ml
Resolution: 0.001
Cell: 10 mm
Back D Next