ChemistryAndSampleTypePage.CHEMISTRY_SELECTION = <HTML><font color="white">Which <A HREF=Help.chemistry>reagents</A> do you want to use to detect the target sequence?</font></HTML>
ChemistryAndSampleTypePage.THERMAL_CYCLING_SELECTION = <HTML><font color="white">Which <A HREF=Help.rampSpeed>ramp speed</A> do you want to include in the instrument run?</font></HTML>
ChemistryAndSampleTypePage.SAMPLE_TYPE_SELECTION = <HTML><font color="white">What type of <A HREF=Help.template>template</A> do you want to use in the real-time PCR reactions?</font></HTML>
ChemistryAndSampleTypePage.TAQMAN = TaqMan\u00AE Reagents
#next line also in messages_en_US.properties
ChemistryAndSampleTypePage.TAQMAN_DESC = The real-time PCR reactions contain two primers and a TaqMan\u00AE probe. The primers are designed to amplify the target sequence. The TaqMan probe is designed to hybridise to the target sequence and generate fluorescence signal when the target sequence is amplified.
ChemistryAndSampleTypePage.SYBR_GREEN = SYBR\u00AE Green Reagents
ChemistryAndSampleTypePage.SYBR_GREEN_DESC = The real-time PCR reactions contain two primers and SYBR\u00AE Green I dye. The primers are designed to amplify the target sequence. The SYBR Green dye generates increased fluorescence signal when it binds to double-stranded DNA. Select "Include Melt Curve" to perform melt curve analysis of the amplified sequence.
ChemistryAndSampleTypePage.CDNA = cDNA (complementary DNA)
ChemistryAndSampleTypePage.CDNA_DESC = You are adding cDNA to the real-time PCR reactions. You have already performed reverse transcription to convert the RNA to cDNA.
ChemistryAndSampleTypePage.RNA = RNA
ChemistryAndSampleTypePage.RNA_DESC = You are adding total RNA or mRNA to the real-time PCR reactions. Select "1-Step RT-PCR" perform reverse transcription (RT) and PCR in one instrument run or select "2-Step RT-PCR" to perform RT and PCR in 2 instrument runs.
ChemistryAndSampleTypePage.GDNA = gDNA (genomic DNA)
ChemistryAndSampleTypePage.GDNA_DESC = You are adding purified gDNA to the real-time PCR reactions. You have already extracted the gDNA from tissue or sample.
ChemistryAndSampleTypePage.UNPROCESSED_TISSUE_SAMPLE = Unprocessed Tissue/Sample
ChemistryAndSampleTypePage.UNPROCESSED_TISSUE_SAMPLE_DESC = You want to add unprocessed tissue or sample to the real-time PCR reactions. To proceed with this quantitation experiment, select a different template type OR extract DNA or RNA from the tissue or sample. Applied Biosystems recommends Applied Biosystems Purification Reagents.
ChemistryAndSampleTypePage.UNPROCESSED_TISSUE_SAMPLE_ERROR = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>You selected unprocessed tissue/sample as your template.<br>To proceed with this quantitation experiment, select a different template type OR extract DNA or RNA from the tissue or sample. <br>To extract DNA or RNA from your tissue or sample, use Applied Biosystems <A HREF=Link.PurificationReagents>Purification Reagents</A>.</TD></TR></TABLE></BODY></HTML>
ChemistryAndSampleTypePage.METHOD_TYPE_SELECTION = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><b><font color=white>Which <A HREF=Help.quantitationMethod>quantitation method</A> are you using?</font></b></TD></TR></TABLE></BODY></HTML>
ChemistryAndSampleTypePage.ABSOLUTE_STANDARD_CURVE = Standard Curve
ChemistryAndSampleTypePage.ABSOLUTE_STANDARD_CURVE_DESC = With the standard curve method, you use standards to determine the absolute quantity of target sequence in a sample.
ChemistryAndSampleTypePage.RELATIVE_STANDARD_CURVE = Relative Standard Curve
ChemistryAndSampleTypePage.RELATIVE_STANDARD_CURVE_DESC = With the relative standard curve method, you use standards, a reference sample, and an endogenous control to determine the relative quantity of target sequence in a sample.
ChemistryAndSampleTypePage.DDCT = Comparative C\u0442 (\u0394\u0394C\u0442) 
ChemistryAndSampleTypePage.DDCT_DESC = With the comparative C\u0442 (\u0394\u0394C\u0442) method, you use a reference sample and an endogenous control to determine the relative quantity of target sequence in a sample.
ChemistryAndSampleTypePage.MELTING_CURVE_ANALYSIS = Include Melt Curve
ChemistryAndSampleTypePage.MELTING_CURVE_ANALYSIS_DESC = Select to add a melt curve stage to the run method and melt curve analysis to the results for experiments using SYBR Green reagents.
ChemistryAndSampleTypePage.FAST_DESC = For optimal results using the Fast ramp speed, Applied Biosystems recommends using Fast reagents for your real-time PCR reactions.
ChemistryAndSampleTypePage.STANDARD_DESC = For optimal results using the standard ramp speed, Applied Biosystems recommends standard reagents for your real-time PCR reactions.
ChemistryAndSampleTypePage.RT_INFO_TEXT = You are adding total RNA or mRNA to the real-time PCR reactions. Select "1-Step RT-PCR" to perform reverse transcription and real-time PCR in one instrument run OR select "2-Step RT-PCR" to perform RT and real-time PCR in two instrument runs.
ChemistryAndSampleTypePage.RT_1_STEP = 1-Step RT-PCR
ChemistryAndSampleTypePage.RT_2_STEP = 2-Step RT-PCR
ChemistryAndSampleTypePage.TAQMAN_RT_2_STEP_INFO_TEXT = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>You selected RNA as your template and to perform 2-step RT-PCR.<br>To proceed with this quantitation experiment, first perform reverse transcription to convert the RNA to cDNA, then select "cDNA" as the template. <br>Applied Biosystems recommends using the <A HREF=Link.HighCapacitycDNAArchiveKit.Taqman>High Capacity RNA-to-cDNA products</A>.</TD></TR></TABLE></BODY></HTML>
ChemistryAndSampleTypePage.SYBR_RT_2_STEP_INFO_TEXT = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>You selected RNA as your template and to perform 2-step RT-PCR.<br>To proceed with this quantitation experiment, first perform reverse transcription to convert the RNA to cDNA, then select "cDNA" as the template. <br>Applied Biosystems recommends using the <A HREF=Link.HighCapacitycDNAArchiveKit.Sybr>High Capacity RNA-to-cDNA products</A>.</TD></TR></TABLE></BODY></HTML>
ChemistryAndSampleTypePage.WARNING = Warning
ChemistryAndSampleTypePage.NO_FAST_OPTION = To use the Fast ramp speed with RNA templates (performing 1-step RT-PCR), use Advanced Setup.

DilutionSeriesPage.VIEW_DETAILS = View Details
DilutionSeriesPage.REACTION_SETUP_REPORT = Print Reaction Setup
DilutionSeriesPage.REACTION_SETUP_REPORT_TOOLTIP = Print reaction setup instructions
DilutionSeriesPage.EXCESS_REACTION_MIX = Excess Reaction Volume:
DilutionSeriesPage.REACTION_VOLUME_PER_WELL = Reaction Volume Per Well:
DilutionSeriesPage.REACTION_MIX_CALCULATIONS = Reaction Mix Calculations
DilutionSeriesPage.SAMPLE_DILUTION_CALCULATIONS = Sample Dilution Calculations
DilutionSeriesPage.ASSAY_TYPE = Assay Type:
DilutionSeriesPage.SELECT_DETECTOR_PRIMER = Select Target
DilutionSeriesPage.REACTION_MIX = Reaction Mix Volume
DilutionSeriesPage.REACTION_MIX_FOR_PROBE = Reaction Mix Volume for {0}
DilutionSeriesPage.MASTER_MIX_FACTOR = Master Mix Concentration:
DilutionSeriesPage.ASSAY_MIX_FACTOR = Assay Mix Concentration:
DilutionSeriesPage.PRIMER_MIX_FACTOR = Primer Mix Concentration:
DilutionSeriesPage.STANDARD_DILUTION_SERIES = Standard Dilution Series
DilutionSeriesPage.STANDARD_DILUTION_SERIES_FOR_PROBE = Standard Dilution Series for {0}
DilutionSeriesPage.FINAL_CONCENTRATION = Diluted Sample Concentration (10X for Reaction Mix):
DilutionSeriesPage.INFO_TEXT = For each target assay in the reaction plate, select the assay type (if using TaqMan reagents), then review the calculated volumes for preparing the standard dilution series, samples, and PCR reactions. If needed, edit the reaction volume, excess reaction volume, component concentrations, and/or stock concentrations. Click "Print Reaction Setup" to print instructions on how to prepare the PCR reactions.
DilutionSeriesPage.STANDARD_STOCK_CONCENTRATION = Standard Quantity in Stock (ng/\u03BCL):
DilutionSeriesPage.STANDARD_STOCK_TARGET_QUANTITY = Standard Quantity (per \u03BCL):

ReactionSetupPage.REVIEW_PIPETTING_OUTPUTS_DESC.StandardCurveMethod = For each target assay in the reaction plate, select the assay type (if using TaqMan reagents), then review the calculated volumes for preparing the standard dilution series, samples, and PCR reactions. If needed, edit the reaction volume, excess reaction volume, component concentrations, and/or stock concentrations. Click "Print Reaction Setup" to print instructions on how to prepare the PCR reactions.
ReactionSetupPage.REVIEW_PIPETTING_OUTPUTS_DESC.RelativeStandardCurveMethod = For each target assay in the reaction plate, select the assay type (if using TaqMan reagents), then review the calculated volumes for preparing the standard dilution series, samples, and PCR reactions. If needed, edit the reaction volume, excess reaction volume, component concentrations, and/or stock concentrations. Click "Print Reaction Setup" to print instructions on how to prepare the PCR reactions.
ReactionSetupPage.REVIEW_PIPETTING_OUTPUTS_DESC.RelativeQuantificationMethodImpl = For each target assay in the reaction plate, select the assay type (if using TaqMan reagents), then review the calculated volumes for preparing the samples and PCR reactions. If needed, edit the reaction volume, excess reaction volume, component concentrations, and/or stock concentrations. Click "Print Reaction Setup" to print instructions on how to prepare the PCR reactions.

PlateThermalProtocolPanel.INFO_TEXT = Review the reaction volume and the thermal profile for the default run method. If needed, edit the default run method or select a run method from the library.
PlateThermalProtocolPanel.SELECT_PROFILE = Select Method:
PlateThermalProtocolPanel.TAQMAN_FAST_PROFILE_NAME = Default Method: Fast Quantitation Using TaqMan Reagents
PlateThermalProtocolPanel.TAQMAN_STANDARD_PROFILE_NAME = Default Method: Quantitation Using TaqMan Reagents 
PlateThermalProtocolPanel.SYBR_PROFILE_NAME = Default Method: Quantitation Using SYBR Green Reagents

GexWizardController.CHEMISTRY_PAGE_TITLE = Methods & Materials
GexWizardController.CHEMISTRY_PAGE_HEADER = Define: Methods & Materials
GexWizardController.CHEMISTRY_PAGE_DESC = Select the quantitation method, reagents, ramp speed, and type of template for the real-time PCR reactions.
GexWizardController.CHEMISTRY_PAGE_TOOLTIP = Select the methods, reagents, and template type for the real-time PCR reactions.
GexWizardController.SAMPLE_PAGE_TITLE = Samples
GexWizardController.SAMPLE_PAGE_HEADER = Set Up: Samples
GexWizardController.SAMPLE_PAGE_TOOLTIP = Set up the samples to test in the reaction plate.
GexWizardController.CALIBRATOR_PAGE_TITLE = Relative Quantitation Settings
GexWizardController.RSC_CALIBRATOR_PAGE_TITLE = Relative Quantitation Settings
GexWizardController.CALIBRATOR_PAGE_HEADER = Set Up: Relative Quantitation Settings
GexWizardController.RSC_CALIBRATOR_PAGE_HEADER = Set Up: Relative Quantitation Settings
GexWizardController.CALIBRATOR_PAGE_DESC = Select the reference sample and the endogenous control to perform relative quantitation.
GexWizardController.RSC_CALIBRATOR_PAGE_DESC = Select the reference sample and the endogenous control to perform relative quantitation.
GexWizardController.CALIBRATOR_PAGE_TOOLTIP = Select the reference sample and the endogenous control.
GexWizardController.RSC_CALIBRATOR_PAGE_TOOLTIP = Select the reference sample and the endogenous control.
GexWizardController.STANDARD_CURVE_PAGE_TITLE = Standards
GexWizardController.STANDARD_CURVE_PAGE_HEADER = Set Up: Standards
GexWizardController.STANDARD_CURVE_PAGE_DESC = Enter the number of points and replicates for all standard curves in the reaction plate. For each standard curve, enter the starting quantity and select the serial factor.\n
GexWizardController.STANDARD_CURVE_PAGE_TOOLTIP = Set up the standards to run in the reaction plate.
GexWizardController.THERMAL_PROTOCOL_PAGE_TITLE = Run Method
GexWizardController.THERMAL_PROTOCOL_PAGE_HEADER = Set Up: Run Method
GexWizardController.THERMAL_PROTOCOL_PAGE_DESC = Review the reaction volume and the thermal profile for the default run method. If needed, edit the default run method or select a run method from the library.
GexWizardController.THERMAL_PROTOCOL_PAGE_TOOLTIP = Review the instrument run conditions.
GexWizardController.REVIEW_PLATE_DESIGN_OUTPUTS_TITLE = Review Plate Layout
GexWizardController.REVIEW_PLATE_DESIGN_OUTPUTS_HEADER = Review Plate Layout
GexWizardController.REVIEW_PLATE_DESIGN_OUTPUTS_DESC = Review the plate layout for the reaction plate, then select one of the options.
GexWizardController.REVIEW_PLATE_DESIGN_OUTPUTS_TOOLTIP = Review the arrangement of real-time PCR reactions in the reaction plate.
GexWizardController.REVIEW_PIPETTING_OUTPUTS_TITLE = Reaction Setup
GexWizardController.REVIEW_PIPETTING_OUTPUTS_HEADER = Set Up: Reaction Setup 
GexWizardController.REVIEW_PIPETTING_OUTPUTS_TOOLTIP = Review the components and volumes for the real-time PCR reactions.
GexWizardController.REVIEW_THERMAL_PROTOCOL_TITLE = Run Method
GexWizardController.REVIEW_THERMAL_PROTOCOL_HEADER = Set Up: Run Method
GexWizardController.REVIEW_THERMAL_PROTOCOL_DESC = Review the reaction volume and the thermal profile for the default run method. If needed, edit the default run method or select a run method from the library.
GexWizardController.REVIEW_THERMAL_PROTOCOL_TOOLTIP = Review the instrument run conditions.
GexWizardController.REVIEW_ANALYSIS_SETTINGS_TITLE = Review Analysis Settings
GexWizardController.REVIEW_ANALYSIS_SETTINGS_HEADER = Review Analysis Settings
GexWizardController.REVIEW_ANALYSIS_SETTINGS_DESC = Select to use default, saved, or custom analysis settings for calculating results and well quality.
GexWizardController.REVIEW_ANALYSIS_SETTINGS_TOOLTIP = Select settings for calculating results.

GexWizardController.PROBE_PAGE_TITLE = Targets
GexWizardController.PROBE_PAGE_HEADER = Set Up: Targets
GexWizardController.PROBE_PAGE_DESC = Enter the number of targets to quantify in the reaction plate, then set up the assay for each target.
GexWizardController.PROBE_PAGE_TOOLTIP = Set up the targets to detect and quantify in the reaction plate.

GexWizardController.SETUP_GROUPING = Set Up
GexWizardController.ORDER_GROUPING = Order (Optional)

StandardCurveSetupPage.DILUTION_POINTS_QN = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font size=3 color=red><b>* </b></font>How many <A HREF=Help.dilutionPoints>points</A> do you need for each standard curve?</TD></TR></TABLE></BODY></HTML> 
StandardCurveSetupPage.REPLICATES_QN = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font size=3 color=red><b>* </b></font>How many <A HREF=Help.replicates>replicates</A> do you need for each point?</TD></TR></TABLE></BODY></HTML> 
StandardCurveSetupPage.STANDARD_CURVE_PREVIEW = Standard Curve Preview
StandardCurveSetupPage.STANDARD_CURVE_PREVIEW_FOR = Standard Curve Preview for
StandardCurveSetupPage.STANDARD_CURVE_PROPERTIES = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>For each standard curve, define the range of standard quantities by entering the <A HREF=Help.startingQuantity>starting quantity</A> and <A HREF=Help.serialFactor>serial factor</A>.<br><br> \
	Define the standard curve so that the range of standard quantities spans the expected range of quantities for the unknowns.</TD></TR></TABLE></BODY></HTML> 
StandardCurveSetupPage.PROBE_NAME = Target Name
StandardCurveSetupPage.STARTING_COPIES = Enter Starting Quantity
StandardCurveSetupPage.UNITS = Enter Units 
StandardCurvePreview.ERROR=Illegal argument for StandardCurvePreview
StandardCurveSetupPage.DILUTION_FACTOR = Select Serial Factor
StandardCurveSetupPage.SETUP_STANDARDS = Set Up Standards
StandardCurveSetupPage.STANDARD_QUANTITY_INFINITE_ERROR = Infinite value. Enter a new number.
StandardCurveSetupPage.STANDARD_QUANTITY_NAN_ERROR = For starting quantity, enter a number greater than 0.
StandardCurveSetupPage.DILUTION_SERIES_PREVIEW = Standard Curve Preview
StandardCurveSetupPage.previewButton.Name = Click here to see preview.

WellCountPanel.WELL_COUNT = Well Count
WellCountPanel.USED_WELLS = Wells Used
WellCountPanel.EMPTY_WELLS = Empty
WellCountPanel.NEGATIVE_CONTROL = Negative Control 
WellCountPanel.SWING_CONSTANTS=Orientation must be SwingConstants.VERTICAL or SwingConstants.HORIZONTAL

GEXPlatePanel.ARRANGE_PLATE = Arrange Plate by:
GEXPlatePreview.EXTRA_WELL1=NOTE: Based on the values you entered, more than {0} wells are required.\n\n
GEXPlatePreview.EXTRA_WELL2=Change 1 or more of the following values to reduce the number of wells to {0} or less:\n\n
GEXPlatePreview.EXTRA_WELL3=\u2022 Number of targets \n
GEXPlatePreview.EXTRA_WELL4=\u2022 Number of targets set up with standards \n
GEXPlatePreview.EXTRA_WELL5=\u2022 Number of points and/or replicates in the standard curve\n
GEXPlatePreview.EXTRA_WELL6=\u2022 Number of samples \n
GEXPlatePreview.EXTRA_WELL7=\u2022 Number of sample/target replicates \n
GEXPlatePreview.EXTRA_WELL8=\u2022 Number of negative controls \n
GEXPlatePanel.PLACE_NTCS = Place Negative Controls in:

SamplesSetupPage.SAMPLES_QN = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font size=3 color=red><b>* </b></font>How many <A HREF=Help.sample>samples</A> do you want to test in the reaction plate?</TD></TR></TABLE></BODY></HTML>
SamplesSetupPage.BIOGROUPS_QN = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font size=3 color=red><b>* </b></font>How many <A HREF=Help.sample>Biological Replicate Groups</A> do you want to test in the reaction plate?</TD></TR></TABLE></BODY></HTML>
SamplesSetupPage.NO_COLUMN=No column with index 
SampleProbeMapPage.HEADING=\nYour selections affect the number of wells required.\nTo change the number of samples, standards,\nor negative controls, go back to Step 4.\n\n
SampleProbeMapPage.SAMPLE=Sample
#next two lines also in messages_en_US.properties
SamplesSetupPage.SELECT_COLOR = Colour
SampleProbeMapPage.NO_COLUMN=No column with index 
SamplesSetupPage.SETUP_SAMPLE_DETAILS_INSTRUCTION = For each sample in the reaction plate, enter a sample name and select a sample colour.
SamplesSetupPage.SETUP_BIOGROUP_INSTRUCTION = Select well(s) in the plate layout, then assign a biological replicate group from the list.
SamplesSetupPage.SPECIFY_COMBINATIONS = Specify Sample/Target Reactions
SamplesSetupPage.USE_ALL_DETECTORS_FOR_ALL_SAMPLES = All Sample/Target Reactions
SamplesSetupPage.SAMPLE_DETECTOR_COMBINATIONS = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font color=white>Which <A HREF=Help.sampleTargetReactions>sample/target reactions</A> do you want to set up?</font></TD></TR></TABLE></BODY></HTML>
SamplesSetupPage.BIOLOGICALGROUP_DEFINITION = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font color=white>Set Up <A HREF=Help.sampleTargetReactions>Biological Replicate Groups</A></font></TD></TR></TABLE></BODY></HTML>
SamplesSetupPage.NO_BIOLOGICAL_GROUPS = No Biological Replicates
SamplesSetupPage.SPECIFY_BIOGROUP = Specify Biological Replicate Groups
SamplesSetupPage.SAMPLE_DETECTOR_REPLICATES = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font size=3 color=red><b>* </b></font>How many <A HREF=Help.replicates>replicates</A> do you need?</TD></TR></TABLE></BODY></HTML>
SamplesSetupPage.NUMBER_OF_NTCS = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><font size=3 color=red><b>* </b></font>How many <A HREF=Help.negativeControl>negative controls</A> do you need for each target assay?</TD></TR></TABLE></BODY></HTML>
SamplesSetupPage.SETUP_SAMPLES = Set Up Samples
SamplesSetupPage.ENTER_SAMPLE_NAME = Enter Sample Name
SamplesSetupPage.SAMPLE_NAME_ERROR=A sample name is required.
SamplesSetupPage.SAMPLE_PAGE_DESC.StandardCurveMethod = Enter the number of samples to test in the reaction plate, enter the number of sample/target reaction replicates, enter the number of negative controls, enter sample names, associate the samples with biological replicate groups, then select the sample/target reactions to set up.
SamplesSetupPage.SAMPLE_PAGE_DESC.RelativeStandardCurveMethod = Enter the number of samples to test in the reaction plate, enter the number of sample/target reaction replicates, enter the number of negative controls, enter sample names, associate the samples with biological replicate groups, then select the sample/target reactions to set up.
SamplesSetupPage.SAMPLE_PAGE_DESC.RelativeQuantificationMethodImpl = Enter the number of samples to test in the reaction plate, enter the number of sample/target reaction replicates, enter sample names, associate the samples with biological replicate groups, then select the sample/target reactions to set up.

SampleProbeCombinationPanel.TABLE_ORIENTATION = Place Samples In
SampleProbeCombinationPanel.NO_COLUMN=No column with index 
SampleProbeCombinationPanel.SAMPLE=Sample

ProbesSetupPage.PROBES_QN = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD><b><font size=3 color=red>* </font></b>How many <A HREF=Help.targets>targets</A> do you want to quantify in the reaction plate?</b></TD></TR></TABLE></BODY></HTML>
ProbesSetupPage.SETUP_STANDARD_CURVE = Set Up Standards
ProbesSetupPage.SETUP_TARGETS = Set Up Targets
#next line also in messages_en_US.properties
ProbesSetupPage.INFO_TEXT.StandardCurveMethod = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>For each target <A HREF=Help.assay>assay</A> in the reaction plate, select whether to set up <A HREF=Help.standard>standards</A>, enter a target name, select the <A HREF=Help.reporter>reporter</A> and <A HREF=Help.quencher>quencher</A> to use to detect the target, and select a <A HREF=Help.targetColor>target colour</A>. (Optional) Enter a gene name, find Applied Biosystems gene expression assays, then select an assay to fill in the <A HREF=assayID>Assay ID</A>.</TD></TR></TABLE></BODY></HTML>
ProbesSetupPage.INFO_TEXT.RelativeStandardCurveMethod = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>For each target <A HREF=Help.assay>assay</A> in the reaction plate, select whether to set up <A HREF=Help.standard>standards</A>, enter a target name, select the <A HREF=Help.reporter>reporter</A> and <A HREF=Help.quencher>quencher</A> to use to detect the target, and select a <A HREF=Help.targetColor>target colour</A>. (Optional) Enter a gene name, find Applied Biosystems gene expression assays, then select an assay to fill in the <A HREF=assayID>Assay ID</A>.</TD></TR></TABLE></BODY></HTML>
ProbesSetupPage.INFO_TEXT.RelativeQuantificationMethodImpl = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>For each target <A HREF=Help.assay>assay</A> in the reaction plate, enter a target name, select the <A HREF=Help.reporter>reporter</A> and <A HREF=Help.quencher>quencher</A> to use to detect the target, and select a <A HREF=Help.targetColor>target colour</A>. (Optional) Enter a gene name, find Applied Biosystems gene expression assays, then select an assay to fill in the <A HREF=assayID>Assay ID</A>.</TD></TR></TABLE></BODY></HTML>
ProbesSetupPage.ENTER_TARGET_NAME = Enter Target Name
ProbesSetupPage.SELECT_REPORTER = Reporter
ProbesSetupPage.SELECT_QUENCHER = Quencher
#next line also in messages_en_US.properties
ProbesSetupPage.SELECT_COLOR = Colour
ProbesSetupPage.FIND_ASSAY = (Optional) Enter Gene Name and Click "Find"
PreviewPanel.EXCESS_WELLS2=Excess Well Requirements:
ProbesSetupPage.ASSAY_ID = Assay ID
ProbesSetupPage.FIND = Find
ProbePage.QUESTION=Obsolete? What are the probes you want to use for each sample and what are they labeled with?
ProbePage.PROBE_NAME=Probe Name
ProbePage.PRODUCTS=Products
ProbePage.NO_COLUMN=No column with index 
PreviewPanel.UNKNOWN=Unknown Wells:
ProbesSetupPage.TARGETS = Targets
PreviewPanel.WELLS_USED=Wells Used: 
ProbesSetupPage.PROBE_NAME_ERROR = A target name is required.
ProbesSetupPage.ASSAY_FOR = Assay for
ProbesSetupPage.NO_COLUMN=No column with index 
PreviewPanel.EXCESS_WELLS=Excess Well Requirements: 

FindAssayCellEditor.ENTER_SEARCH_TERM = Enter Gene Name
FindAssayCellEditor.ENTER_SEARCH_TERM_MESSAGE = Enter a gene name to search for an assay.
FindAssayCellEditor.SEARCH_IN_PROGRESS = Search in Progress
FindAssayCellEditor.SEARCH_WAIT = Searching for an assay...
FindAssayCellEditor.FIND = Find
FindAssayCellEditor.NOT_FIND = No results match your search in the Applied Biosystems Store.

DDCtSettingsPage.ASK_CALIBRATOR = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>Which sample do you want to use as the <A HREF=Help.referenceSample>reference sample</A>?</TD></TR></TABLE></BODY></HTML>
DDCtSettingsPage.ASK_ENDOGENOUS_CONTROL = <HTML><BODY><TABLE CELLSPACING=0 CELLPADDING=0 ><TR><TD>Which target do you want to use as the <A HREF=Help.housekeepingControl>endogenous control</A>?</TD></TR></TABLE></BODY></HTML>

GEAssaySelectionTableModel.AVAILABILITY = Availability
GEAssaySelectionTableModel.COLUMN_INDEX=Column index out of range: 
GEAssaySelectionDialogMouseListener.NOT_AVAILABLE=This action is not available at this time.
GEAssaySelectionDialogMouseListener.WEB_LINK=Web Link:
GEAssaySelectionTableModel.ASSAY_ID = Assay ID
GEAssaySelectionTableModel.GENE_SYMBOL = Gene Symbol
GEAssaySelectionTableModel.GENE_NAME = Gene Name
GEAssaySelectionTableModel.REF_SEQ  = RefSeq
GEAssaySelectionDialog.FIND=Find Assay Results
GEAssaySelectionDialog.APPLY=Apply Assay Selection
GEAssaySelectionDialog.CANCEL=Cancel
GEAssaySelectionDialog.FIRST=First
GEAssaySelectionDialog.LAST=Last
GEAssaySelectionDialog.NEXT=Next >
GEAssaySelectionDialog.PREVIOUS=< Previous
GEAssaySelectionDialog.CURRENT=Current Page
GEAssaySelectionDialog.DESCRIPTION = {0} Assays Found. Click the Assay ID to view the assay in the Applied Biosystems Store. Select an assay to detect and quantify the target sequence. {2}
GEAssaySelectionDialog.FOUND=\ Assays Found 
GEAssaySelectionDialog.SELECT=\ Click the Assay ID to view the assay in the Applied Biosystems Store. Select a row in the table, then click "Apply Assay Selection."
GEAssaySelectionDialog.OF=\ of 
GEAssaySelectionDialog.NO_PAGE1=There is no page numbered '
GEAssaySelectionDialog.NO_PAGE2=' in the search results.
GEAssaySelectionDialog.NO_PAGE3=Find Assay Results
GEAssaySelectionDialog.ABC=abc
GEAssaySelectionDialog.TARGET=Target 123

GexExperimentWizard.EXPERIMENT_DESC = Design a gene quantitation experiment to determine the amount of target nucleic acid sequence in a sample.
GexExperimentWizard.DISPLAY_NAME = Quantitation

GEXAssaySearchPanel.ENTER_KEY = Enter Gene Name
GEXAssaySearchPanel.FOLLOWER = Enter a gene name, then click "Find Assay" to search the Applied Biosystems Store for a gene expression assay.
GEXAssaySearchPanel.ENTER_SEARCH_TERM = Enter Search Term
GEXAssaySearchPanel.ENTER_SEARCH_TERM_MESSAGE = Enter a search term
GEXAssaySearchPanel.FIND = Find
GEXAssaySearchPanel.NOT_FIND = No results match your search in the Applied Biosystems Store.
GEXAssaySearchPanel.SEARCH_IN_PROGRESS = Search in Progress
GEXAssaySearchPanel.SEARCH_WAIT = Searching for an assay...
GEXAssaySearchPanel.ASSAY_FOR = Assay for
GEXAssaySearchPanel.MI_RNA_MSG=<HTML><BODY>If you are looking for miRNA assays, click <A HREF=http://www.appliedbiosystems.com/products/miRNA.html>here</A></BODY></HTML>"

WellPage.PREVIEW1=Make sure you leave space for your\nunknowns\!\n\n
WellPage.PREVIEW2=The number of unknown wells required\nwill be determined when you map\nprobes to samples on step 6.
ReviewAnalysisSettingsPage.DEFAULT=* Default Settings *
ReviewAnalysisSettingsPage.PROTOCOL=Analysis Protocol
ReviewAnalysisSettingsPage.PROTOCOL_TITLE=Absolute Standard Curve Analysis
ReviewAnalysisSettingsPage.AUTOMATIC=Automatic Baseline
ReviewAnalysisSettingsPage.MANUAL=Manual Baseline
ReviewAnalysisSettingsPage.BROWSE=Browse...
ReviewAnalysisSettingsPage.CANCEL=Cancel
ReviewAnalysisSettingsPage.AUTOMATIC_CT=Automatic C\u0442
ReviewAnalysisSettingsPage.MANUAL_CT=Manual C\u0442
ReviewAnalysisSettingsPage.END=End
ReviewAnalysisSettingsPage.USE_STANDARD=Use standard curve in plate
ReviewAnalysisSettingsPage.USE_SAVED=Use saved standard curve
ReviewAnalysisSettingsPage.START=Start
ReviewAnalysisSettingsPage.THRESHOLD=Threshold
ReviewAnalysisSettingsPage.PROBES=Targets
PreviewPanel.STANDARD=Standard Wells:
PreviewPanel.NTC=Negative Control Wells:
PreviewPanel.ENDO=Endogenous Control Wells:
PreviewPanel.EMPTY=Empty Wells:
QuantitationPage.DDCT=\u0394\u0394C\u0442
QuantitationPage.STANDARD=Standard Curve
QuantitationPage.DISSOCIATON=Include Melt Curve Analysis
QuantitationPage.METHOD=3. Select Quantitation Method
QuantitationPage.STANDARD_DESCRIPTION=Determines the absolute quantity of a nucleic acid target sequence within an unknown sample by reference to a standard curve
QuantitationPage.MELT_DESCRIPTION=Dissociation curve analysis of nucleic acids using SYBR Green I dye.
QuantitationPage.DDCT_DESCRIPTION=Determines the change in expression level of a target gene sequence in a test sample relative to a calibrator sample
QuantitationPage.QUESTION=Which quantitation method do you want to use?
ProbePage.INFO=7. Probe Information
ProbePage.TYPE=Type
# the following line also in messages_en_US.properties for U.S. English
ProbePage.COLOR=Colour
ProbePage.DYES=Dyes
ProbePage.GENE=Gene (Optional)
ProbePage.FAM=FAM-MGB
ProbePage.VIC=VIC-MGB
ProbePage.VIEW=View Inventoried/Made to Order Assays
RunPlateNowOrEditSetupPage.LABEL=<html><table width=150><tr><td>Open the experiment for advanced editing</td></tr></table></html>
RunPlateNowOrEditSetupPage.RUN_PLATE=<html><table width=150><tr><td>Run plate on instrument</td></tr></table></html>
