beautypg.com

2 routine method group, Routine method group – Eppendorf BioSpectrometer basic User Manual

Page 33

background image

33

Methods

Eppendorf BioSpectrometer

®

basic

English (EN)

6.2.2

Routine method group

The methods for the

Routine group are preprogrammed as fixed methods. Therefore, a new method name

is required after the method parameters in the fixed preprogrammed methods have been modified.

Nucleic acids

• Determination of the concentration of nucleic acids through measurement at 260

nm

and

evaluation

via

factor.

• Various nucleic acid methods, such as dsDNA or RNA, are preprogrammed. The parameters vary

according to the factor.

• Preprogrammed method for microliter cuvettes: Measuring DNA in sample volumes within the

microliter range with 1 mm light path (with microliter cuvettes as Eppendorf μCuvette

G1.0

or

Hellma

®

TrayCell).

• Additional information on the purity of the measured nucleic acid: Ratios A260/A280, ratios A260/A230,

absorbance wavelength spectrum of nucleic acid, absorbance of the background wavelength (preset:
320

nm; the absorbance of the pure nucleic acid should be close to zero here).

• Partial turbidity correction can be performed via the

Background parameter.

• Concentrations can be converted to molar concentrations and (after the sample volume has been

entered) to nucleic acid quantities (

process results method step).

Proteins direct UV

• Determination of the concentration of proteins via measurement at 280

nm and factor or standard

evaluation.

• Preprogrammed methods for direct absorbance output as a result

(Protein

A

280) and for evaluation via

albumin-specific absorbance coefficients

(Albumin

A

280).

• Preprogrammed method for microliter cuvettes: Measuring protein in sample volumes in the microliter

range with 1

mm light path (with microliter cuvettes as Eppendorf μCuvette

G1.0 or Hellma

®

TrayCell).

• Additional information on the purity of the measured protein: Absorbance of the background

wavelength (preset: 320

nm; the absorbance of the pure protein should be close to zero here).

• Partial turbidity correction can be performed via the

Background parameter.

• When programming the methods, the corresponding factor is imported through the simple selection of

the protein from a predefined list. The factors are separately defined in the functions of the

Gen.

method param. group. Various proteins are preprogrammed in Gen. method param.; additional
proteins can be added.

Proteins (with reagent)

• Concentration determination of proteins via measurement according to color reactions and evaluation

using standards or factors (typical: evaluation with standard curve).

• The

Bradford, Bradford micro, Lowry, Lowry micro, BCA and BCA micro methods are already

preprogrammed. According to the reagent manufacturer, the "Curve fit" (standard curve type) must be
changed as necessary.