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GrainGenes Sequence Report: NSFT03P2_Contig15569

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Sequence	BF292264
Contig	NSFT03P2_Contig15569
Tracefile	[ Download ] [ View ]
External Databases	Data at GenBank Data at EMBL Data at DDBJ
wEST map position	BF292264
DB Remark	Locus Source: Aegilops speltoides
Keyword	EST
Species	Aegilops speltoides
Cultivar	F2 from 2-12-4-8-1-1-1-(1) x PI36909-12-811-(1 ) F2 from 2-12-4-8-1-1-1-(1) x PI36909-12-811-(1)
Chromosome	7AS 7DS
Clone Library	Aegilops speltoides anther cDNA library
Tissue	Anther
Developmental Stage	Premeiotic anthers
Data Source	genbank Release 135, Apr 15 2003 genbank Downloaded 2008-2009
Title	WHE2208_F05_L10ZS Aegilops speltoides anther cDNA library Aegilops speltoides cDNA clone WHE2208_F05_L10, mRNA sequence.
Other Name	WHE2208_F05_L10ZS  [ wEST-mySQL (obsolete) ]
Strain	lab_host E. coli SOLR
DNA Library	AS040E1X
Clone	WHE2208_F05_L10
Probe	WHE2208_F05_L10
Remark	DB_xref: taxon:4573 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 a growth chamber at the University of California, Davis (Akhunov). Premeiotic anthers were harvested, total RNA and poly(A) RNA were prepared, from each tissue and then pooled, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab (Akhunov, Chin, Choi, Close, Fenton, Kianian, Otto, Simons , Zhang) 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 a growth chamber at the University of California, Davis (Akhunov). Premeiotic anthers were harvested, total RNA and poly(A) RNA were prepared, from each tissue and then pooled, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab (Akhunov, Chin, Choi, Close, Fenton, Kianian, Otto, Simons, Zhang) at the University of California, Riverside. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA Homology	TaAffx.53150.1.S1_at 200 WHE2AFFY TaAffx.53150.1.S1_at 194 WHE2AFFY TaAffx.53150.1.S1_at 70 WHE2AFFY TaAffx.117132.1.S1_at 178 WHE2AFFY TaAffx.117132.1.S1_at 135 WHE2AFFY
DNA	ggaatcggcgcccacctccgccgccgccatgtcgccgtctctgctcgggg ggctcaccaagtcgctggccatgaccgtgctctccgaggtcggcgacaag accttcttcgccgccgcgcaggatgttcgacgatatgccgccgccgccgg cggtggctgtgctgtatcagcggactaggggaggagtcaggcggcggcag ctgcagatttcgcccaggcgctgaccaaattcctggatcaatagccggga tcagctcgccagcagcgagatcttagctgagattagcagcagctcggctc atctcacctgctcctttttctaattaaagaaaagcagaggagtactagct cggttctctgctcctctattagtggaaatcggctgttttcttggatgatg aatcaccctgcctgctaattctggccatgcgccatccccggaagctcgtc cttgctggctgtctatcggcgttaacagtgatgacggctttatctgcttc tctaggctgggttgcaccaaacctgatatcacgtaaatggactcatcata tcaccactctgct

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