| Products/Services Used | Details | Operation |
|---|---|---|
| Gene Synthesis> | The purified PCR product was ligated into the clone vector, pMD-18T (TAKARA), and then transformed into E. coli stain DH5α. After identification, positive clones were sequenced using T7 primers (GENSCRIPT, China). | Get A Quote |
In this paper, we firstly reported a C-type lectin cDNA clone of 1029 bps from the larvae of A. Pernyi (Ap-CTL) using PCR and RACE techniques. The full-length cDNA contains an open reading frame encoding 308 amino acid residues which has two different carbohydrate-recognition domains (CRDs) arranged in tandem. To investigate the biological activities in the innate immunity, recombinant Ap-CTL was expressed in E. coli with a 6-histidine at the amino-terminus (Ap-rCTL). Besides acted as a broad-spectrum recognition protein binding to a wide range of PAMPs and microorganisms, Ap-rCTL also had the ability to recognize and trigger the agglutination of bacteria and fungi. In the proPO activation assay, Ap-rCT... More