Table 2.
Primer sequences used for fusion constructions in this study.
| Primer | Order | Sequence (5’→3’) | Gene BankAccession No. |
|---|---|---|---|
| huIL-15 | Forward | CACCGGTACCAACTGGGTGAATGTAATAAGTGATTTG | NM_172175 |
| Reverse | CGGGATCCAGAAGTGTTGATGAACATTTGGAC | ||
| huIgHg2 | Forward | CACCGGATCCGCCTCCACCAAGGGCCCAT | AJ250170 |
| Reverse | GCTCTAGATCATTTACCCGGAGACAGGGAGAGGCTCTTCTGT | ||
| mIL-15 | Forward | TAGGTACCGGCATTCATGTCTTCATTTTGG | NM_008357 |
| Reverse | TAGGATCCGGACGTGTTGATGAACATTTGG | ||
| mIgHg2a | Forward | AGGATCCGCCAAAACAACAG | KC295246.1 |
| Reverse | TCTAGAATCATTTACCCGGAGTCC |
The nucleotide sequence for each gene was procured from the Gene Bank (NCBI). The Accession numbers were given for each sequence. The primers having restriction enzyme recognition sequences were designed by using PrimerQuest Tool (Integrated DNA Technologies) and OligoPerfect Designer (Thermo Fisher Scientific). The HPLC purified primers (Sigma Aldrich) were used.