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GrainGenes Sequence Report: NSFT03P2_Contig15028

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Sequence	BE425967
Contig	Ta.1357.1.S1_at Ta.1357.3.S1_a_at NSFT03P2_Contig15028
Tracefile	[ Download ] [ View ]
External Databases	Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index	TC307068
wEST map position	BE425967
DB Remark	Locus Source: Triticum aestivum (bread wheat)
Keyword	EST
Germplasm	Chinese Spring
Species	Triticum aestivum
Cultivar	Chinese Spring
Chromosome	6AL 6BL 6DL
Clone Library	Wheat unstressed seedling shoot cDNA library
Tissue	Etiolated shoot
Developmental Stage	Five day old seedling
Data Source	genbank Release 135, Apr 15 2003 genbank Updated Nov 2006
Title	WHE0326_D02_G04ZS Wheat unstressed seedling shoot cDNA library Triticum aestivum cDNA clone WHE0326_D02_G04, mRNA sequence.
Other Name	WHE0326_D02_G04ZS  [ wEST-mySQL (obsolete) ]
Strain	lab_host E. coli SOLR
DNA Library	TA006E1X
Clone	WHE0326_D02_G04
Probe	WHE0326_D02_G04
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; 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. Shoots were harvested. The tissue, 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; 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. Shoots were harvested. The tissue, 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.1357.1.S1_at 1023 WHE2AFFY [ Show all 7 ]
DNA	atttggtcagcttacggcctaggaacctggagcctcgtgtagcagttgga tttgcattggacatcgcccgagccatggaatgtttgcatgcacatgggat cattcatcgtgatcttaaacctgagaatctgctgcttacagcagaccaga gaacagttaagctcgtcgaccttggtttagcaagagaagagacgttaaca gagatgatgaccgcagaaacaggaacataccgttggatggctcctgagtt gtacagcacagtcacattaaggcacggagaaaagaaacattacaaccaca aagtagatgtttacagctttgcgattgtgttatgggaactactacacaat agactaccctttgagggcatgtctaacctgcaagctgcatatgctgccgc tttcaagaacatcagaccaagtgcagataatttgccggaggagctgtcag agatcctaacatcctgctggaaagaagacccaagcgacagaccaaacttc acccagatagttcaaatgcttctccattacctctcaaccctttcaccgcc agaacatatggccccggctcgcacattcagttcggagaatgcaatcttac ctcctgaatcgcctgggacgagctctctaatggcttctc

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