Table 1.
Primer | Sequence (5′ to 3′) |
---|---|
cDNA library development | |
Template switch (TS) | AAGCAGTGGTATCAACGCAGAGTACGCrGrGrG |
TRsa(T)30 | CGCAGTCGGTACT30 |
CapPCR | AAG CAG TGG TAT CAA CGC AGA GTA |
Cloning primers | |
Lu4Cap | CGACGTGGACTATCCATGAACGCAAAGCAGTGGTATCAACGCAGAGTA |
Lu4TRsa | CGACGTGGACTATCCATGAACGCACGCAGTCGGTACT30 |
NsLu4 | TCGAGCGGCCGCCCGGGCAGGTCGACGTGGACTATCCATGAACGCA |
CbCCAPr.5.F | CCTACGTCTTGGTGGCTCTC |
CbCCAPr.8.R | TAATCTTGGCCTTTGGGATG |
CbCCAPr.4.R | AAGGGGAAGGTGATGACGGTCACT |
CbCCAPr.7.F | ATCGATTTCCCGAAGTTGTG |
Tissue distribution PCR primers | |
CbCCAPr.5.F | CCTACGTCTTGGTGGCTCTC |
CbCCAPr.8.R | TAATCTTGGCCTTTGGGATG |
Cbβtub.1.F | TCTGTGCTGGATGTAGTCCG |
Cbβtub.3.R | AGAGTGGCGTTGTATGGCTC |
qRT-PCR primers | |
CbCCAPr.3.F | GGTGGCTCTGACTGTCTTCCTCTT |
CbCCAPr.4.R | AAGGGGAAGGTGATGACGGTCACT |
aPrimers used for development of cDNA libraries suitable for RACE, cloning of CbCCAPr, tissue distribution, and qRT-PCR measurements. βtub, Beta-tubulin; F, forward; R, reverse.