VCT-1&2 (ctx gene encoding Vibrio cholerae enterotoxin)
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SEE-1&2 (see (entE) gene encoding staphylococcal enterotoxin E)
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SED-1&2 (sed (entD) gene encoding staphylococcal enterotoxin D)
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SEZ-1&2 (sec (entC) gene encoding staphylococcal enterotoxin C)
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SEA-1&2 (sea (entA) gene encoding staphylococcal enterotoxin A)
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EVC-1&2 (Genes of the Verocytotoxin type 1 and 2 (VT1, VT2, VT2vha, VT2vhb, VT2vpl; Shiga-like toxin type I and II) of EHEC, or VTEC
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EVS-1&2 (Genes of the Verocytotoxin type 2 (VT2, VT2vha, VT2vhb, VT2vpl; Shiga-like toxin type II) of EHEC, or VTEC
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EVT-1&2 (Genes of the Verocytotoxin type 1 (VT1:Shiga-like toxin type I) of enterohemorrhagic E. coli (EHEC), or Verocytotoxin-producing E. coli (VTEC)
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ESP-1&2 (Gene of the heat-stable enterotoxin for human (STp) of ETEC
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ESH-1&2 (Gene of the heat-stable enterotoxin for human (STh) of ETEC
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ELT-1&2 (Gene of the heat-labile enterotoxin (LT) of enterotoxigenic E. coli (ETEC)
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VPS-1&2 (Thermostable direct hemolysin-related hemolysis (Trh1) gene of Vibrio parahaemolyticus)
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VPD-1&2 (Thermostable direct hemolysin (tdh) gene of Vibrio parahaemolyticus)
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Frequently asked questions
What are M13 primers and why are they still the default?
M13 forward and reverse primers anneal to fixed sites flanking the polylinker in M13mp and pUC-derived vectors, so one pair sequences almost any insert cloned into them. That is why they remain the standard for clone verification — no primer design per construct, and no synthesis wait, since they are stocked as catalog oligos.
What is the difference between a primer, a linker and an adaptor?
A primer is a short single-stranded oligo that anneals to a template so a polymerase can extend from it. A linker is a short double-stranded oligo carrying a restriction site, ligated onto blunt ends to create a cloning handle. An adaptor is similar but arrives with a compatible overhang already formed, so it ligates directionally — the basis of directional cDNA cloning and library construction.
What does the solid support do in oligonucleotide synthesis?
Phosphoramidite synthesis builds the oligo base by base on a solid particle, and the support's loading capacity determines how much product a given column delivers. Cytiva's Primer Support 5G is a cross-linked polystyrene support loaded at 350 µmol/g for DNA and 300 µmol/g for RNA, supporting oligos of around 70 bases and scale-up from 1 µmol to 750 mmol.
Can I order custom-synthesised oligos from this category?
Not from these listings. This category holds catalog primers, linkers and cloning vectors, plus the consumables used to manufacture oligos — it is not a custom synthesis service. For custom primers, probes or modified oligos, contact Danyel Biotech directly and we will route the request to the right supplier and come back with a quote.

