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GrainGenes Sequence Report: BE590634

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Sequence
BE590634
Contig
Ta.9592.1.S1_at
Ta.9592.1.S1_x_at
NSFT03P2_Contig16006
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC303504
wEST map position
BE590634
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
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1AL
1BL
Clone Library
Wheat 20-45 DAP spike cDNA library
Tissue
Spike and seed
Developmental Stage
Adult plant
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE0858_A03_B06ZS Wheat 20-45 DAP spike cDNA library Triticum aestivum cDNA clone WHE0858_A03_B06, mRNA sequence.
Other Name
WHE0858_A03_B06ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA017E1X
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; Sequence have been trimmed to remove vector sequence and low; quality sequence with phred score less than 20; Seq primer: Stratagene SK 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 Homology
Ta.9592.1.S1_at979WHE2AFFY
Ta.9592.1.S1_x_at979WHE2AFFY
Ta.341.1.S1_at309WHE2AFFY
Ta.341.1.S1_at70WHE2AFFY
TaAffx.30658.1.S1_at54WHE2AFFY
DNA
caatggcggcggcggcgaacggcgggggcggggagaccaagcggcgttcg
cgcggatctacgacgcgctcaaggcggagctgctccgggaccccgccttc
gagtacacggagtcgtcgcaccagtggatcgaccgcatgctggactacaa
tgtactgggaggaaagtgcaaccgtgggctctctgtggtcgatagctata
agctgttgaaaggcgtcgatgttcttaccgaggaggagatgtttcttgcc
tccactctcggttggtgcattgaatggcttcaagccttctttcttgtgct
cgatgatatcatggacgactcccacactcgacgtgggcagccttgttggt
ttagggtgcctcaggttggcttcattgctgtaaatgatgggattctcctt
cgcaaccatatttcgagaatgcttcggctccactttaagaagaagcctta
ctatgccgatctccttgatttattcaacgaggttgagttcaagacagctt
ctggtcaaatgctggaccttattacaacccacgagggagaaaaagatcta
acgaaatataacattggg

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