Table 1 |
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|
Oligonucleotide primers |
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| Domain |
PCR primer (5'-3') |
RE |
|
|
||
| 10 kDa |
F: catgggatcctggaagaaaaagagagaaag |
BamH I |
| R: catgctcgagtcagggtgagtgagtggataag |
Xho I |
|
| 16 kDa |
F: catgggatcctttcgatacagtggccggact |
BamH I |
| R: catgctcgagtcatgcttctgtgggctctggct |
Xho I |
|
| 22 kDa |
F: catgggatccttccgaactcttaacatcaatgggcaaa |
BamH I |
| R: catgctcgagtcactcatcagcaatctcggtctcc |
Xho I |
|
| 30 kDa |
F: catggaattcatgcactgcaaggtttctttgt |
EcoR I |
| R: catgctcgagtcatttggatcctagcgcaag |
Xho I |
|
| PfJ |
F: catgcatgcatatgcctgaagtagttccacaagaa |
Nde I |
| R: catgggatccttatgcactttcacctccccc |
BamH I |
|
|
|
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|
Forward (F) and reverse (R) primer sequences were designed for amplifying the different human 4.1R domain sequences and P. falciparum 4.1R binding sequence (PfJ) in EBA-181. Endonuclease recognition sequences are underlined and the corresponding restriction enzyme (RE) indicated. |
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Lanzillotti and Coetzer Malaria Journal 2006 5:100 doi:10.1186/1475-2875-5-100 |
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