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GrainGenes Sequence Report: NSFT03P2_Contig13724

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Sequence	BE606654
Contig	NSFT03P2_Contig13724
Tracefile	[ Download ] [ View ]
External Databases	Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index	TC291711
wEST map position	BE606654
NCBI UniGene	Ta.49781
DB Remark	Locus Source: Triticum aestivum (bread wheat) UniGene title 'Clone wlm96.pk032.n8:fis, full insert mRNA sequence'
Keyword	EST
Germplasm	Chinese Spring
Species	Triticum aestivum
Cultivar	Chinese Spring
Chromosome	5AS 5BS 5DS
Clone Library	Wheat 5-15 DAP spike cDNA library
Tissue	Spike
Developmental Stage	Adult plant
Data Source	genbank Release 135, Apr 15 2003 genbank Updated Nov 2006
Title	WHE0901_E06_I11ZS Wheat 5-15 DAP spike cDNA library Triticum aestivum cDNA clone WHE0901_E06_I11, mRNA sequence.
Other Name	WHE0901_E06_I11ZS  [ wEST-mySQL (obsolete) ]
Strain	lab_host E. coli SOLR
DNA Library	TA018E1X
Clone	WHE0901_E06_I11
Probe	MAG1727 WHE0901_E06_I11
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 5, 10 and 15 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 5, 10 and 15 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.878.1.S1_at 658 WHE2AFFY Ta.1705.1.S1_x_at 84 WHE2AFFY Ta.1705.1.S1_x_at 64 WHE2AFFY
DNA	ttgacaaggagcttaagcaaataacgaaagataaaaatgaagctgtccgt ggccaggattttgagaaggctggagagttgcgagatcgtgaaatggaatt gaaggcccagataacagccttgattgacaagagcaaggagatgaacaaag cagagactgagtcgggagagactgggccgatggtgcatgaatcagatatc cagcacattgtgtcatcatggactggtattccagtggagaaagtctcgac tgacgaatctgataaacttcttaagatggaagagacattgcataagcgtg tcatcggccaagacgaggctgtgaaagcaataagtcggtctgttcgccgt gctcgtgtgggcctcaagagccccaacagaccaattgcgagcttcatttt tgcaggtcccactggtgttgggaaatcagagcttgcaaagactc

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