biochrom GeneQuant 1300 Quick Reference Manual page 7

Parameter Folder
Pathlength Applications
Life science
Peak detect on Applications
zoom
Phosphorylated Life Science
Prime Life Science
concentration
Printer Utilities
Replicates Applications
Life Science
Sort peaks by Applications
Standards Applications
Life Science
Start RNA Life science
Start Applications
wavelength
Std. n (n=a Applications
number) Life Science
T Life Science
Theme Utilities
Units Applications
Life Science
TM
GeneQuant 1300 Quick Reference Guide Page 7
Sub-Folder
Absorbance Ratio -
Parameters
Nucleic Acids – DNA
Nucleic Acids – RNA
Nucleic acids – Oligo
Tm Calculation
Cy Dye
Protein – Protein UV
Wavescan, options 4 –
peak detection
Tm Calculation
Tm Calculation
Printer
Standard curve
Protein – BCA
Protein – Bradford
Protein – Lowry
Protein – Biuret
Wavescan, options 4 –
peak detection
Standard curve
Protein – BCA
Protein – Bradford
Protein – Lowry
Protein – Biuret
Cy Dye
Wavescan
Standard curve
Protein – BCA
Protein – Bradford
Protein – Lowry
Protein – Biuret
Nucleic Acids - Oligo
Preferences
Absorbance Ratio –
Parameters
Nucleic acids – DNA
Nucleic acids – RNA
Nucleic acids – Oligo
Protein – Protein UV
Manual Description and options
page
58 Select the relevant path length – 5 or 10
mm
13
15
17
21
23
28
48 Yes/No – determines whether peaks are
reassessed and tabulated when the user
zooms into a region of the wavescan or
whether these stay as determined on the
un-zoomed display
21 Select whether or not the sample is
phosphorylated: yes or no
21 Enter the concentration of the primer.
62 Select the printer to send the results to.
Options: Built in (internal printer), or to a
computer via either USB port or Bluetooth
53 Select the number of standards to be
30 measured and averaged at each standard
33 concentration point. Options: OFF (=1), 2 or
36 3. This parameter is only available if the
39
calibration mode is set to Standards
48 Select how peaks are sorted – by
wavelength, peak height or peak width
53 Enter the number of standard concentration
30 points to be used in the curve. Range 1-9.
33
36
39
23 The amount of RNA in ng that is being used
47 Enter the start wavelength for the spectral
scan – range 200 – 950 nm
54 Enter the concentration value for each
30 standard. These parameters are only
33 available if the calibration mode is set to
36 Manual
39
17 Enter the proportion of Thymine bases.
Default is 10, range: 0 – 9999. Only an
option when units are pmol/µl
63 Define the screen layout of folders. Options
are a grid format (the default) or a list
58 Select the units to measure the absorbance
ration in. Options: µg/ml, ng/µl or µg/µl
13
15
17
28
Version 2.0