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# Copyright:    (c) 2006 Applied Biosystems. All Rights Reserved.
# $Revision: 9630 $
# $Date: 2006-09-20 09:27:29 -0700 (Wed, 20 Sep 2006) $
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# U.S. English version of strings in messages.properties.
#
# There are few differences between en_AU, en_CA, en_GB, en_SG, en_ZA, etc., but many differences
# between those and en_US. It is therefore more efficient to put international English spellings in
# messages.properties, and put U.S-specific spellings here in messages_en_US.properties

SamplesSetupPage.SELECT_COLOR = Color
SamplesSetupPage.SETUP_SAMPLE_DETAILS_INSTRUCTION = For each sample in the reaction plate, enter a sample name and select a sample color.

MarkersSetupPage.AIF_NO_TABLE_HEADER = For each SNP assay in the reaction plate, enter a SNP assay name, enter a gene name or refSNP ID (optional), and select a SNP assay color. For each allele, enter an allele name or the base(s) to detect, select the reporter and quencher to detect the allele, and select an allele color.


ChemistryAndSampleTypePage.TAQMAN_DESC = The PCR reactions contain two primers and two TaqMan\u00AE probes. The primers are designed to amplify the sequence containing the SNP. Each TaqMan probe is designed to hybridize to one allele sequence and generate fluorescence signal when the allele sequence is amplified.
ChemistryAndSampleTypePage.DNA_DESC = You are adding the purified, resuspended DNA to the final reaction mix. Use an optimized protocol to extract the DNA. Then, make sure the A260/280 ratio is greater than 1.7, the DNA does not contain PCR inhibitors, agarose gel electrophoresis shows the DNA is intact, and the DNA has not been heated above 60 \u00B0C.

ChemistryAndSampleTypePage.DRY_DNA_DESC = You are drying down the purified, resuspended DNA in wells of an optical reaction plate. Use an optimized protocol to extract the DNA. Then, make sure the A260/280 ratio is greater than 1.7, the DNA does not contain PCR inhibitors, agarose gel electrophoresis shows the DNA is intact, and the DNA has not been heated above 60 \u00B0C.

