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GrainGenes Sequence Report: CD452377

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Sequence
CD452377
Contig
Ta.22871.1.S1_s_at
NSFT03P2_Contig16225
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC300118
wEST map position
CD452377
NCBI UniGene
Ta.54574
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Gamma-type tonoplast intrinsic protein'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
3DS
4AL
4BL
Clone Library
CS wheat unstressed seedling shoot normalized cDNA library
Tissue
Etiolated shoot
Developmental Stage
Five day old seedling
Data Source
genbankRelease 136, Jun 15 2003
genbankUpdated Nov 2006
Title
WHE1060_E08_I16ZT CS wheat unstressed seedling shoot normalized cDNA library Triticum aestivum cDNA clone WHE1060_E08_I16, mRNA sequence.
Strain
lab_host E. coli DH10B
Clone
WHE1060_E08_I16
Probe
WHE1060_E08_I16
Remark
DB_xref: taxon:4565
Feature: source: mol_type = 'mRNA';
Locus Comment: Contact: Olin Anderson; US Department of Agriculture, Agriculture Research Service, Pacific; West Area, Western Regional Research Center; 800 Buchanan Street, Albany, CA 94710, USA; Tel: 5105595773; Fax: 5105595818; Email: oandersn@pw.usda.gov; This EST was generated by sequencing from the 3' end of the clone.; Sequences have been trimmed to remove vector sequence and low; quality sequence with phred score less than 20.; Seq primer: T7 primer.
Note: Vector: Lambda Uni-ZAP XR, excised phagemid pBluescript SK; Site_1: EcoRI; Site_2: XhoI; Seeds were surface-sterilized, germinated and grown aseptically in the dark at room temperature on filter paper with water, nystatin and cefotaxime in covered crystallization dishes. Roots were harvested. The tissue, total RNA, and poly(A) RNA were prepared, a cDNA library was made in the TJ Close lab (Choi, Close, Fenton) at the University of California, Riverside. The cDNA clones were in vivo excised to give pBluescript phagemids before normalization was carried out. The mass excision of phagemid library and normalization were done in HT Nguyen lab by D. Zhang at Texas Tech Univeristy. Normalization protocol used was that of Soares'. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA
tttttttttttttttttttttttttttttttcaacccaactcaacttgaa
attactcgggcgggacgggcgaattcacagttttacagaagcaaattgag
agtgtcgtccagggttttacagctccacgaactcaccacaaactgatcga
cccaggaagcaaacttaaacgactcatggtgatggcaaggaaggagacga
cgcgatcatagatcacacggacggacgggcaggcaggcggcgggcttgca
cgcaagcaagcaggctggctgcgctgagctcgctgctcagtagtcggtgg
tggggagctgctcgtgggtgcgggagatgaagagcagctcgtaaatgacg
ccggcgaggccgccgccgatgagggggccgacccagtacacccactggta
cccccactcccagctgacgagggcggggccgaaggagacggcggggttca
tggacgcgccggaaaagct

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