XB-CLONE-1507418
Sequence:
5' EST: EE313097
[+]
gcactggctctggtttcacatccctgctgatggagcgtctctctgtcgactatggaaagaagtccaagctggagtttgccatctaccccgctcctcaagt
ctccactgctgtggtcgaaccttacaactctatcctaaccacccacaccaccttggagcactctgactgtgctttcatggtggataacgaggccatctac
gatatctgtcgcagaaacctcgacattgagcgaccaagctacaccaacctcaaccgtctcattggtcagatcgtgtcctccattactgcttcactgcgct
tcgatggggccctgaacgtcgatctgactgagttccagaccaatttggtgccctatcccagaatccacttccctctggtcacatactctcccatcatctc
tgctgagaaggcctaccacgagcagctgtctgtgtctgagatcaccagcgcctgctttgagccttccaatcagatggtgaagtgtgatcctcgccatggc
aagtacatggcctgctgtatgctgtatcgtggtgatgtcgtacccaaagatgtgaatgctgccattgccaacattaagaccaaacgctccattcagtttg
tggactggtgtccaactggattcaaggtcggcatcaactaccagccaccaactgtggttcctggtggagacttggccaaaggtacagagagccgtgtgca
tgttgagcaacaccacggctattgctgagcctgggctcgtctggaccacaagttcgatctgatgtatgccagcgcgcctttgtacactgggtatgtgtga
cgtatggagacgagagttctctgagcagagagatctgctgcactggagaggatacgaaggaagtggcgcagacctctacgagatgggaagaggcaaggga
3' EST: EE323034
[+]tgaagaagacaaagacagcttacaaaacaaagtgctttcacagacagaaaatgcctttggcaacagtttctttgaactcagacagaaaagtggtatagaa
aaagaatgaaaccggacacaacagaacatgtataaatcacacacaccagggcattgtttcccattactgggattcataaggcagcttggcaatggagagg
taaacactaattagaagtgctggagttggaccagtttctcttctgactcctggccagggtttaaaactggtctcagatcagctttttgaagcatctttaa
tactcctctccttcctctccatcctccgtagagtctgcgccaacctcctcgtaatctttctccagtgcggcaagatcctctctggcctcagagaactctc
cttcttccataccttcaccaacataccagtgtacaaaggcgcgcttggcatacatcagatcgaacttgtggtccagacgagcccaggcctcagcaatagc
cgtggtgttgctcaacatgcacacggctctctgtaccttggccaagtctccaccaggaaccacagttggtggctggtagttgatgccgaccttgaatcca
gttggacaccagtccacaaactgaatggagcgtttggtcttaatgttggcaatggcagcattcacatctttgggtacgacatcaccacgatacagcatac
agcagccatgtacttgccatgcgaggatcacacttcacatctgattggaagctcaaagcagcgctgtgatcctcagaaccagacagctgctcgtgtagct
tctcagcaagatgatgggagagtatgtgaccgagatggattctggataggcacaaatgtctgaactcatcgatcgacgtcagccatcgacccatgaccgt
atgagacgactgacatgacgtagtagtactgtcgctcacgtccagagct
Library:
Description: cDNA was primed using oligo-dT primer: GACTAGTTCTAGATCGCGAGCGGCCGCC(T)25 and cloned into the SmaI/NotI sites of pCS111. Size-selection >1.25kb resulted in an average insert size of 1.7 kb. This primary library was constructed by Express Genomics (Frederick, MD). Note: this is a Xenopus Gene Collection library.Vector Details | Vector Map |
Name: pCS111
Type: plasmid
5' Restriction Site: SmaI
3' Restriction Site: NotI |  |
Usage:
Suppliers: