© Gunnar Wrobel & Felix Kokocinski,
DKFZ
, 2003 - 2009
Basic parameters
eg APOM
eg ENSG00000111964
eg ENSMUST00000025846
Aedes aegypti
Anolis carolinensis
Anopheles gambiae
Bos taurus
Caenorhabditis elegans
Callithrix jacchus
Canis familiaris
Cavia porcellus
Choloepus hoffmanni
Ciona intestinalis
Ciona savignyi
Danio rerio
Dasypus novemcinctus
Dipodomys ordii
Drosophila melanogaster
Echinops telfairi
Equus caballus
Erinaceus europaeus
Felis catus
Gallus gallus
Gasterosteus aculeatus
Gorilla gorilla
Homo sapiens
Loxodonta africana
Macaca mulatta
Macropus eugenii
Meleagris gallopavo
Microcebus murinus
Monodelphis domestica
Mus musculus
Myotis lucifugus
Ochotona princeps
Ornithorhynchus anatinus
Oryctolagus cuniculus
Oryzias latipes
Otolemur garnettii
Pan troglodytes
Pongo pygmaeus
Procavia capensis
Pteropus vampyrus
Rattus norvegicus
Saccharomyces cerevisiae
Sorex araneus
Spermophilus tridecemlineatus
Sus scrofa
Taeniopygia guttata
Takifugu rubripes
Tarsius syrichta
Tetraodon nigroviridis
Tupaia belangeri
Tursiops truncatus
Vicugna pacos
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.