Primer Design

Primers can be designed directly against the sequences annotated in CnidoSite, or against a sequence you paste in. Design is performed by primer3 (version 2.6.1) running on this server — your sequence is not sent to any third-party website. For reference, the primers released with this database were designed with an optimal melting temperature of 60°C (58–62 °C), an optimal primer length of 20 bp (18–24 bp), and a GC content between 40% and 60%, with self-complementarity restricted to limit primer-dimer formation; that parameter set is the CnidoSite published protocol preset below.

Template taken from CnidoSite: g3739.t1 (g3739.t1), 399 bp.
Template

Two ways to supply a template: pick a species and a gene / transcript ID, or paste your own sequence. If the gene ID is found it is used; the pasted sequence is used otherwise. A template must be at least 30 bp.

Load example sequence
Primer parameters
Advanced parameters (any field left empty keeps the preset value)

A value that is not a number is ignored. The product size range is applied only when both of its fields are filled in and the maximum is at least the minimum.

Melting temperature
Primer length and GC content
Product and output
Self-complementarity and probe
Download TSV
Design results sorted by primer3 penalty, lowest first

Template 399 bp · parameter preset CnidoSite published protocol (Tm 60 [58-62] °C, 20 [18-24] bp, GC 40-60%) · 5 primer pairs returned.

Pair Left primer (5'→3') Position Len Tm (°C) GC (%) Right primer (5'→3') Position Len Tm (°C) GC (%) Product (bp) Penalty
1 TTGAAGTACGACGCAACGGA 214–233 20 59.969 50.000 TGCTGTGACATTGCAGTTGC 349–368 20 59.969 50.000 155 0.062
2 TGTTTCGCGTCGGAGAAGAA 180–199 20 59.969 50.000 TGCTGTGACATTGCAGTTGC 349–368 20 59.969 50.000 189 0.062
3 TGGGCATGGGTATTTCGCTT 152–171 20 60.034 50.000 TGCTGTGACATTGCAGTTGC 349–368 20 59.969 50.000 217 0.065
4 TTGGGCATGGGTATTTCGCT 151–170 20 60.034 50.000 TGCTGTGACATTGCAGTTGC 349–368 20 59.969 50.000 218 0.065
5 CCTCCTCCTCCAAGCGTTTT 268–287 20 59.963 55.000 TGCTGTGACATTGCAGTTGC 349–368 20 59.969 50.000 101 0.068
Primer map pair 1 (lowest penalty) · product 155 bp at template position 214–368 · the two tracks are drawn at different scales

Left primer — binds the template strand as listed (5′→3′)Right primer — its reverse complement binds hereProduct

Template399 bpproduct 155 bp · template 214–368product 155 bpleft primer, template 214–233right primer anneals here, template 349–3681101200300399Amplicon155 bpleft primer TTGAAGTACGACGCAACGGA · 5′→3′right primer TGCTGTGACATTGCAGTTGC · its reverse complement binds the template strandTTGAAGTACGACGCAACGGATGCTGTGACATTGCAGTTGCinterior 115 bp214253291330368
Left primer
TTGAAGTACGACGCAACGGA
template 214–233 · 20 bp · Tm 59.969 °C · GC 50.000 %
Right primer
TGCTGTGACATTGCAGTTGC
template 349–368 · 20 bp · Tm 59.969 °C · GC 50.000 %

Amplicon sequence (5′→3′ on the template strand, 155 bp) — blue is the left primer, red is where the right primer anneals. Copy from here to order or to check a base by eye.

TTGAAGTACGACGCAACGGACAACATACCGTATGCAGGGGCCAAATTCAGCAGTCCTCCTCCTCCAAGCGTTTTGCCAAAGCCGCCATCGCATTGGATAACTTCTCCCATCATCCATCATTTCGACGTGGACGTCGCAACTGCAATGTCACAGCA

The right primer is listed as its own 5'→3' sequence; what anneals to the template strand shown here is its reverse complement, so the highlighted stretch is complementary to the listed sequence. That is expected.

How to read this table. Position is a 1-based interval on the template, and both primers use the same convention: it is the stretch the primer occupies on the template strand (for the left primer, starting at its 5’ end; for the right primer, the region it anneals to, i.e. where the reverse complement of the listed sequence sits on the template). The two coordinates in a row can therefore be subtracted directly, and the amplicon view above marks both of them so you can check them by eye. Penalty is primer3’s weighted sum of the deviations from your constraints — lower is better, and the pairs are returned in that order. Tm is computed by primer3 from the SantaLucia thermodynamic parameters at the salt and primer concentrations in effect. The primer sequences themselves are 5’→3′ and can be ordered as they stand; the right primer anneals to the template as its reverse complement.

Specificity has not been assessed. This page only designs primers; it does not check whether they also anneal elsewhere in the genome or transcriptome. Once you have candidates, confirm each primer sequence with this site’s BLAST. The Tm and GC settings above are the design targets, and the annealing temperature still has to be optimised at the bench.

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