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GrainGenes Sequence Report: CD453739

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Sequence
CD453739
Contig
Ta.9592.1.S1_at
Ta.9592.1.S1_x_at
NSFT03P2_Contig16006
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC297943
wEST map position
CD453739
NCBI UniGene
Ta.54800
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Transcribed locus, moderately similar to NP_001056204.1 Os05g0543400 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1AL
1BL
Clone Library
CS wheat 20-45 DAP spike cDNA library
Tissue
Spike and seed
Developmental Stage
Adult plant
Data Source
genbankRelease 136, Jun 15 2003
genbankUpdated Nov 2006
Title
WHE0858_A03_B06ZT CS wheat 20-45 DAP spike cDNA library Triticum aestivum cDNA clone WHE0858_A03_B06, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE0858_A03_B06
Probe
WHE0858_A03_B06
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. Spikes at 20 DAP and seeds at 30 to 45 DAP were harvested, 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. Spikes at 20 DAP and seeds at 30 to 45 DAP were harvested, 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
ttttttttttttttttttttaaagggcagggtgcaaattacagaaccatc
agtcgtctacaccaaagcggtccatcaaacccgaaatagcaccttgcatc
attattactgggagcagcaaggcacaacatacaacatgaagcactaaacc
ataaaatcaacaccgctagtcatctatcaaacatgcaacaaggaacagat
ttcctgcccaagagacaccccctacttctgcctcatgtagatcttgtgca
agaaggacttcagaaccttctgaacaggaacgctcggctgggcttcgata
tcagcaatcagcttcttgtagctctcgctctcgtactcatgaaataccgc
ctcaaggttaagttctttgtagagatccttcacttttgccacacatgctg
gatctttctttccatagttttcaaatagaatgctcttttggctctcatca
gcatgctcaagagcttggacaactagccaggagcacttgtaatcttcaat
gtcggtgccgatcttgccaataaattcaggatcaccataacagtccagat
aatcatcctgaacttggaagtaagttcccatctcaacaagtatgttctct
acagcaccgtagttctccaaactctcaccagagagtagtagcgcacatgc
aaccggcagataaaatgaatagtaggctgtcttgaattgaacaattcggc
ggtggaccccaatgttatatttcgtt

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