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GrainGenes Sequence Report: CD454287

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Sequence
CD454287
Contig
Ta.21357.1.S1_at
NSFT03P2_Contig16230
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC278679
wEST map position
CD454287
NCBI UniGene
Ta.48370
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Clone wlmk1.pk0037.b8:fis, full insert mRNA sequence'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1AL
1BL
1DL
Clone Library
CS wheat pre-anthesis spike cDNA library
Tissue
Spike before anthesis
Developmental Stage
Adult plant
Data Source
genbankRelease 136, Jun 15 2003
genbankUpdated Nov 2006
Title
WHE1777_G07_N13ZT CS wheat pre-anthesis spike cDNA library Triticum aestivum cDNA clone WHE1777_G07_N13, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE1777_G07_N13
Probe
WHE1777_G07_N13
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; Site_1: EcoRI; Site_2: XhoI; Plants were grown in the greenhouse. Whole spike with awns trimmed, white, green and yellow anther were collected and total RNA, and poly(A ) RNA were prepared, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab (Choi, Close, Fenton) at the University of California, Riverside. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
Note: Vector: Lambda Uni-ZAP XR, excised phagemid; Site_1: EcoRI; Site_2: XhoI; Plants were grown in the greenhouse. Whole spike with awns trimmed, white, green and yellow anther were collected and total RNA, and poly(A) RNA were prepared, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab (Choi, Close, Fenton) at the University of California, Riverside. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA
ttttttttttttttttttgcaaaaatgcatacaagacagacatgaatact
caagaattcatatcattagttgtgagttttgcatggcaaaatgtagcata
tacaacttaggtcacagcccatcacatgcagcacgagttgcaaacttatt
gcaagtctggaccaccaacaaatagaacagggggggagaactacaagtca
atactttttatgtccacacatgtttcaccgttggtgacagcagatggtta
accctggctacgcggcattacattacatttcaagacaagcaaatttcttg
cgtccaccgtaagcacatatttcctgtgaccaagtgaaattagaatcagc
cttgctatcttctgctttgtcctccaactgctggtgttttggctacacat
gcagctacaatcatatcttgggacccaaaaactttggtgcgattagaatt
tgtgtttcacatttactaaagaatcacaaggaaatagtctgctatgcttg
gagttgatctcgtgggtgccaaccgccct

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