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: ANN11103-RA (ANN11103-RA), 870 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 870 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 GGCGTCACTGAGAACAAGGA 262–281 20 59.966 55.000 TGTTGGCATCAGCTTGTTGC 375–394 20 59.968 50.000 133 0.066
2 GGAGGCGTCACTGAGAACAA 259–278 20 59.966 55.000 TGTTGGCATCAGCTTGTTGC 375–394 20 59.968 50.000 136 0.066
3 AGGCGTCACTGAGAACAAGG 261–280 20 59.966 55.000 TGTTGGCATCAGCTTGTTGC 375–394 20 59.968 50.000 134 0.066
4 GCAACAAGCTGATGCCAACA 375–394 20 59.968 50.000 AGCCCACCATAACTGAACCG 563–582 20 60.035 55.000 208 0.068
5 CGGTTCAGTTATGGTGGGCT 563–582 20 60.035 55.000 CTGGTGGTCCTTGTCCCTTC 666–685 20 59.963 60.000 123 0.072
Primer map pair 1 (lowest penalty) · product 133 bp at template position 262–394 · 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

Template870 bpproduct 133 bp · template 262–394product 133 bpleft primer, template 262–281right primer anneals here, template 375–3941218436653870Amplicon133 bpleft primer GGCGTCACTGAGAACAAGGA · 5′→3′right primer TGTTGGCATCAGCTTGTTGC · its reverse complement binds the template strandGGCGTCACTGAGAACAAGGATGTTGGCATCAGCTTGTTGCinterior 93 bp262295328361394
Left primer
GGCGTCACTGAGAACAAGGA
template 262–281 · 20 bp · Tm 59.966 °C · GC 55.000 %
Right primer
TGTTGGCATCAGCTTGTTGC
template 375–394 · 20 bp · Tm 59.968 °C · GC 50.000 %

Amplicon sequence (5′→3′ on the template strand, 133 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.

GGCGTCACTGAGAACAAGGACCCTCTTGGAAAAAGAAATGGAAAAGCACCTGGTGAGAAAATGGCAGAAGTCTTAAACAGAACTCGAACAGAAGCAAAGGCTAAAGTTTCCAAGCAACAAGCTGATGCCAACA

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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