© Gunnar Wrobel & Felix Kokocinski,
DKFZ
, 2003 - 2007
Basic parameters
eg APOM
eg ENSG00000111964
eg ENSMUST00000025846
Aedes aegypti
Anopheles gambiae
Apis mellifera
Bos taurus
Caenorhabditis briggsae
Caenorhabditis elegans
Canis familiaris
Cavia porcellus
Ciona intestinalis
Ciona savignyi
Danio rerio
Dasypus novemcinctus
Drosophila melanogaster
Echinops telfairi
Erinaceus europaeus
Felis catus
Fugu rubripes
Gallus gallus
Gasterosteus aculeatus
Homo sapiens
Loxodonta africana
Macaca mulatta
Monodelphis domestica
Mus musculus
Myotis lucifugus
Ornithorhynchus anatinus
Oryctolagus cuniculus
Oryzias latipes
Otolemur garnettii
Pan troglodytes
Rattus norvegicus
Saccharomyces cerevisiae
Sorex araneus
Spermophilus tridecemlineatus
Takifugu rubripes
Tetraodon nigroviridis
Tupaia belangeri
Xenopus tropicalis
mM
nM
°C
nucleotides
HTML
XML
TEXT
Specific AutoPrime parameters
nucleotides
Extended Primer3 settings
nucleotides
nucleotides
°C
°C
°C
%
%
nucleotides
nucleotides
nucl.
°C
°C
°C
Internal oligo options
nM
nucleotides
nucleotides
nucleotides
°C
°C
°C
%
%
nucleotides
AutoPrime
allows to rapidly design primers for real-time PCR measurement of eukaryotic expression. Such primers are usually selected so that they will amplify cDNA generated from mRNA but will not yield a product on the genomic DNA. This is achieved by taking advantage of the eucaryotic splicing system for mRNA. Either primer pairs are selected so that one of the primers matches the exon-exon border sequence that is not present in the genomic sequence or the pair is designed by placing each primer in a different exon so that a genomic product would include a long intronic sequence.
AutoPrime
provides these capabilities on top of the primer3 primer-design software.