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GrainGenes Sequence Report: BE637585

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Sequence
BE637585
Contig
NSFT03P2_Contig18875
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC316115
NCBI UniGene
Ta.28610
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Low-molecular-weight glutenin storage protein'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
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
WHE0860_B05_C10ZS Wheat 20-45 DAP spike cDNA library Triticum aestivum cDNA clone WHE0860_B05_C10, mRNA sequence.
Other Name
WHE0860_B05_C10ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA017E1X
Clone
WHE0860_B05_C10
Probe
BE637585
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
ttcctcgtctttgccctcctcgccgttgcggcgacaagtgcaattgcgca
gatggagactagatgcatccctggtttggagagaccatggcagcagcaac
cattaccaccacaacagacatttccacaacaaccactattttcacaacaa
caacaacaacaactatttcctcaacaaccatcattttcgcagcaacaacc
accattttggcagcaacaaccaccattttctcagcaacaaccaattctac
cacagcaaccaccattttcgcagcaacaacaactagttctaccgcaacaa
ccaccattttcacagcaacaacaaccagttttacctccacaacaatcacc
ttttccacaacaacaacaacaacaccaacagctggtgcaacaacaaatcc
ctgttgttcagccatccattttgcagcagctaaacccatgcaaggtattc
ctccagcagcaatgcaaccctgtggcaatgccac

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