Sequences
Forward (5′→3′)
TGGAGTGACGGAATCTGTGGReverse (5′→3′)
ACGTTGGAGTCTGGTTCCCTAmplicon
150 bp
Primer Tm (°C)
| Conditions | Forward | Reverse | Average | Δ F/R |
|---|---|---|---|---|
| qPCR master mix | 63.2 | 64.8 | 64.0 | 1.6 |
| Primer-BLAST default | 59.4 | 60.8 | 60.1 | 1.4 |
qPCR master mix: Owczarzy 2004/2008 · 250 nM primer · 50 mM Na⁺ · 3 mM Mg²⁺ · 0.8 mM dNTP
Primer-BLAST default: SantaLucia 1998 salt corr. · 50 nM primer · 50 mM Na⁺ · 1.5 mM Mg²⁺ · 0.6 mM dNTP
Bold, underlined base = 3′ end (polymerase extension point).
Primer QC
GC% · Forward
55.0%GC% · Reverse
55.0%Self-dimer ΔG · Fwd (any position)
-0.2 kcal/molSelf-dimer ΔG · Fwd (3′ end)
No duplex foundSelf-dimer ΔG · Rev (any position)
-3.0 kcal/molSelf-dimer ΔG · Rev (3′ end)
0.7 kcal/molHeterodimer ΔG (F×R, any position)
-2.2 kcal/molHeterodimer ΔG (F×R, 3′ end)
0.1 kcal/molΔG at 37 °C · SantaLucia 1998 NN parameters · < −6 kcal/mol = significant dimer risk · "3′ end" is restricted to duplexes anchored at a primer's own 3′ terminal base (polymerase-extendable); "any position" is the most stable duplex anywhere in the primer. Estimated screening value. For comprehensive dimer analysis, validate with Primer3.
Source
Citation
Chen et al. 2025Genomic mapping
★ = Ensembl canonical transcript (reference model, not necessarily the most expressed isoform)
Showing: ENSOART00020099538 ★
Off-target specificity
SpecificNo paired forward+reverse off-target amplicon found against nt (whole genome/transcriptome). Screen requires >=2 total mismatches including >=2 within the last 5bp at the 3' end to clear a hit (NCBI Primer-BLAST-style stringency); hits with >=6 total mismatches are dropped as implausible.
Efficiency measurements
Ideal range:Dilution series 1.90–2.10·LinRegPCR 1.70–1.90·unknown method: not scoredAnalyse your qPCR run with LinRegPCR efficiency correction and a MIQE 2.0 report.