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GrainGenes Sequence Report: BG274294

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Sequence
BG274294
Contig
NSFT03P2_Contig17415
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
wEST map position
BG274294
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
1AL
Clone Library
Aegilops speltoides anther cDNA library
Tissue
Anther
Developmental Stage
Premeiotic anthers
Data Source
genbankRelease 135, Apr 15 2003
genbankDownloaded 2008-2009
Title
WHE2226_H03_O06ZS Aegilops speltoides anther cDNA library Aegilops speltoides cDNA clone WHE2226_H03_O06, mRNA sequence.
Other Name
WHE2226_H03_O06ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
AS040E1X
Clone
WHE2226_H03_O06
Probe
WHE2226_H03_O06
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
Ta.3225.1.S1_at807WHE2AFFY
Ta.3225.1.S1_x_at807WHE2AFFY
Ta.23108.3.S1_x_at48WHE2AFFY
DNA
tcaacgaggacttctacaagcgcacgctctccggcggcgtcgtcacgctc
atctccgccctcgtcatgctgctcctctttgtctccgagaccaggtcgta
ttattattcagcaaccgagactaagttagtggtagacacatcaagaggag
aaaggctaagagtaaattttgatattactttcccgagtattccttgcacc
cttctcagtgttgatacaagggatattantggcgagcagcggcaggacat
taggcatgacattgaaaagaaaagattggactcacatggtaatgtcattg
aatcaagaaaagagggcattggtggaacaaagatcgagaaaccattgcaa
aaacatggtggaaggcttggcaaaggcgaggaatattgtggcacctgtta
tggtgcagaggagtcagatgaacaatgctgtaattcatgtgaagaagtta
gggaggcctacaagaagaaagggtgggctcttacaaaccctgacctaatc
gac

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