Table 1. Ectonucleotidases primer sequences for PCR experiments.
Primer sequence | (T°C) | Fragment size (bp) | |
NPP1 F | 5′- TGG GTT GAA ACC AAG CTG TGC CA -3′ | 69 | 94 |
NPP1 R | 5′- ACA GGC AGC ATC ACA GCG ACA -3′ | ||
NPP2 F | 5′- AGG AGG AGC TCG TTC CAG T -3′ | 59 | 116 |
NPP2 R | 5′- TCC CAT CCT TCT GCT CTC TT -3′ | ||
NPP3 F | 5′- GCA GGT GGA CCA GTC AGT GCC -3′ | 69 | 90 |
NPP3 R | 5′- CCG CTG CTT CAG GCC TTC CA -3′ | ||
NTPDase1 F | 5′- AGT ATG GGA TTG TGC TGG ATG -3′ | 54 | 147 |
NTPDase1 R | 5′- TCT GAA CAA ATT TTG AGA TTC CAG -3′ | ||
NTPDase2 F | 5′- CAG GAT GTG CCC AAA GAG A -3′ | 61 | 685 |
NTPDase2 R | 5′- CCC CAT TGA AAG AGC ATC G -3′ | ||
NTPDase3 F | 5′- TTT CCC TGG ACA CCT TCA AC -3′ | 55 | 184 |
NTPDase3 R | 5′- TGT ATT TGG GGC CAA GTC TC -3′ | ||
NTPDase5 F | 5′- GCA TTT GCC AAC ACC TTT TT -3′ | 55 | 179 |
NTPDase5 R | 5′- ACA GGG CTC TCT GTG ATG CT -3′ | ||
Ecto-5′NT/CD73 F | 5′- AGG GGT GTG GAC GTC GTG GT -3′ | 65 | 84 |
Ecto-5′NT/CD73 R | 5′- CCC AGC AGG CAC CTC TTT GGA -3′ | ||
ADA F | 5′- GGG GAG CGA GAC TTC CGG GGT -3′ | 69 | 83 |
ADA R | 5′- TCC ACC ACC TTG GGG GAC CA -3′ | ||
ALP F | 5′- CAT TGG CAC CTG CCT TAC TA -3′ | 59 | 104 |
ALP R | 5′- GCT CCA GGG CAT ATT TCA GT -3′ | ||
GAPDH F | 5′- TTC TTT TGC GTC GCC AGC CG -3′ | 64 | 93 |
GAPDH R | 5′- ACC AGG CGC CCA ATA CGA CC -3′ |
Primer sequences for PCR experiments. These primers listed here were used for both RT-PCR and real time PCR reactions with exception of primers for amplification of NTPDase2 coding sequences. Melting curve analysis was performed to determine the specificity for each real-time PCR reaction.