★ Founders price. 40% off the first two years of an annual plan started by June 30, 2027, then the standard price. See the plans →
← Primer database

Primer database

NSUN2

NOP2/Sun RNA methyltransferase 2

Rattus norvegicus

PublicationTian et al. 2023

Sequences

Forward (5′→3′)

CGCTGCTATCTGCTCGTCCATC

Reverse (5′→3′)

CTGTGAGTCTAGGAATGCTGGATGC

Amplicon

94 bp

estimated from mapping

Primer Tm (°C)

ConditionsForwardReverseAverageΔ F/R
qPCR master mix66.766.366.50.5
Primer-BLAST default63.463.263.30.2

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

59.1%

GC% · Reverse

52.0%

Self-dimer ΔG · Fwd (any position)

-0.3 kcal/mol

Self-dimer ΔG · Fwd (3′ end)

No duplex found

Self-dimer ΔG · Rev (any position)

-1.2 kcal/mol

Self-dimer ΔG · Rev (3′ end)

-0.3 kcal/mol

Heterodimer ΔG (F×R, any position)

-2.5 kcal/mol

Heterodimer ΔG (F×R, 3′ end)

-1.7 kcal/mol

ΔG 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

PMID

36685826(Europe PMC)

Citation

Tian et al. 2023

Genomic mapping

Ensembl gene

ENSRNOG00000017254 ↗

NCBI Gene ID

361191

Assembly

GRCr8

Cross-check

✓ENSRNOT00000023641★
✓ENSRNOT00000090884
✓ENSRNOT00000161739
✓ENSRNOT00000094155
173bp158bp105bp106bp72bp85bp~193bpThis is the outer span across every isoform's exon here. They don't all agree on the exact boundary (alternative splice site), so hover a row's own box below for its real length.75bp~177bpThis is the outer span across every isoform's exon here. They don't all agree on the exact boundary (alternative splice site), so hover a row's own box below for its real length.74bp131bp97bp182bp93bp136bp81bp139bp40bp2.6kb
exon presentprimer binds hereconfirmed amplicongap = exon skipped~bp = boundary varies
How do I read this diagram?

Each row is one transcript, aligned on a shared axis. A gap means that isoform skips this exonic region. Each row's box is drawn at that isoform's own real exon length, which can be narrower than the column (alternative splice site); hover a box for its exact size. A ~amber header bp means isoforms don't all agree on this region's boundary, while a plain header means they do. Navy blocks mark where the primers bind, and green (with a ✓ by the name) means this isoform has a confirmed working amplicon, not just exon overlap. A row with a “‹ exons” / “exons ›” hint instead of any box means that isoform's exons exist but sit outside the current scroll position (a truncated isoform or alternate transcription start site) — click the hint to jump to them. Click a row to load it below.

★ = Ensembl canonical transcript (reference model, not necessarily the most expressed isoform)

Showing: ENSRNOT00000023641 ★

173bp1436bp158bp2790bp105bp33.4kb106bp42.0kb72bp5808bp85bp61.4kb193bp72.1kb75bp81.5kb131bp93.0kb74bp10685bp131bp11643bp97bp122.0kb182bp13539bp93bp14760bp136bp15666bp81bp16453bp139bp171.5kb40bp182.9kb2.6kb19FRPredicted from the amplicon's own GC%+length (von Ahsen et al. 2001, at the same qPCR buffer as the primer Tm above: 50 mM Na⁺ plus 3 mM Mg²⁺ less 0.8 mM dNTP, as a sodium equivalent), not the SantaLucia model used for primer Tm, which isn't valid at this length. A screening estimate for ranking amplicons — that relation was fitted on oligonucleotide duplexes, so applying it at amplicon length carries more error than its published ±1.9 °C, and it is not a melt-peak prediction.94 bp amplicon · predicted amplicon Tm 86.7 °C
NSUN2 · ENSRNOT00000023641 (NM_001108403) · canonical⚠ Single-exon · may amplify genomic DNA

Off-target specificity

Specific

No 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 scored
No measurements yet for this primer pair.

Using these primers?

Analyse your qPCR run with LinRegPCR efficiency correction and a MIQE 2.0 report.

Analyse your data →