PRIMERCAT · qPCR

qPCR Primer Design

Generate qPCR primer candidates from a gene or DNA sequence, with paired genome and transcript evidence when versioned local references are available

1
Enter Gene Name
Human · Mouse
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2
Design & Screen
Primer3 · Paired screen · Candidate ranking
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3
Compare Candidates
CSV Export · HTML Report
OUTPUTPrimer candidates
Awaiting input
5′Exon structure3′
Candidate 01Exon-spanning preferred
Tm
— °C
GC
— %
Product
— bp
Specificity
Pending

Enter a target to see candidate sequences, quality metrics, and screening evidence.

TXSelect reference transcript by rule
EXExon-spanning design
SPPaired genome / transcript screen
RKComponent status and candidate ranking
qPCR PRIMER DESIGN

Online qPCR primer design: inputs, outputs, and evidence boundaries

PrimerCat accepts standard human or mouse gene symbols as well as custom DNA sequences. Forward and reverse primers are always reported 5′→3′, ready for ordering as shown.

Reference sequence

Gene mode selects an NCBI RefSeq transcript using stated rules and retains its accession, species, and selection basis in the result.

Generation and screening

Primer3 generates candidates under length, Tm, GC%, amplicon, and thermodynamic constraints, followed where available by paired screening against fixed genome and transcriptome references.

How to interpret results

The candidate rank score compares pairs returned in the same run; it is not an experimental success probability. Validate efficiency, melt curves, product identity, and negative controls before use.