XB-CLONE-2454628
Sequence:
5' EST: EL863915 [+]
caagaaaccagggtgttattcttcataagactgaagcagaacacacctttactttccttctgcagctctaattaaaccacaattgccatggatctggtct
ctgtacttctgtctgttgtcatttgcatattcctatataaagtcttctatggaggggaaaaagaatctcagaacttccctcctgggcccaaaccattacc
gatcatcggaaattttcatatgataaatatgaagaaaccccatctaacatttatggagctggctaagaagtacggctcagtattcagcattcagctcggc
ccagagaaactcgttgtggtttgtggcgctgacgcagtgaaagacgctcttgtcaaccatgccgatgagttttcagcgaggcccaccattccggtattcg
ataagacttcaaagggacacggtgtttttttttgctaatggtgagaactggaaagtgatgagaagattcactctttctacactaagagactttgggatgg
gcaagaaaaccatagaagacaggatctgtgaagaaagtgactttttaatggaaacgttcaagtcctataaagggaagccgtttgataacaccatgataat
gaatgcggctgtagccaacatcattgtgcacatactgctcaaccaccgctttgactatcaggatccaacgctgctcaagcttataaacatagtcagtgag
aatatcagcattgctgcaaaaccaatcgttctgctatataatgcctatccgtctattatggaatgggttcccggaactcacaaaagtgtcgctgagaaca
tgttgaaa
3' EST: EL863916 [+]tttttttttttttttgaataaagagttttatttgtgatgtgatttgctctagctgcgaggcaaagcacagatctgatgctccagcggtttggatgtaatt
gcatcggcacaagttagatcgacctcaactccaggagggggttggaatgtgaagttctgcagtaactttgtgaagaacaagaagagttccatcttggcca
atgtctctccgacgcaaattcttcgacctgcagagaagggaaggaaggcctcatttttcacaaaatttccttccgagtcaaggaaatgttccgggtaaaa
ttcttctggctttttgaaataatctttatcttggagaacagatgtcagcagtattatcacttgggttccctttggaataaaataacccctgaatgtgacg
tccgtagttgtttcatggccaacattaggtgcaaggtttcctaatctctgaatctcatggataacggcatcagtatagggcatttttttccgatgttcga
gccgaggttgcgccgatccaatcactttgtcaatttcatcttggacttttttttgaatgtctggatatttcattatgaacaagaggccccagcgaagagt
ggtagaagtcgtctccattccggcaccaaataaatcggctaaaagtactgtcagattttggtcattaaagaactttgtagaagaaggtttctcctcttgt
tgcttgaccagaaatacatcgatgagatccctctggtcatttacgtccagttgatccctgtgttgggtaaatgtctctctgagaaagttgtatagtttca
acatgttct
Library:
Description: The library was made from dT primed cDNA and cloned into vector pCS107. PolyA RNA were primed with an oligo dT primer (5'-GACTAGTTCTAGATCGCGAGCGGCCGCCCTTTTTTTTTTTTTTT -3'), ligated to a SalI adapter (5'-TCGACCCACGCGTCCG-3' and 5'-CGGACGCGTGGG-3') and digested with NotI. cDNA was size selected using 1.1% agarose gel electrophoresis (>0.6kb) then ligated into NotI and SalI digested pCS107 vector. Primary library, non-amplified. Library constructed at the DOE Joint Genome Institute (Walnut Creek, CA) as part of the Xenopus Gene Collection project.Vector Details | Vector Map |
Name: pCS107
Type: plasmid
5' Restriction Site: SalI
3' Restriction Site: NotI | |
Usage:
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