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GrainGenes Sequence Report: BG262826

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Sequence
BG262826
Contig
Ta.5046.1.S1_at
NSFT03P2_Contig14223
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC325027
wEST map position
BG262826
NCBI UniGene
Ta.45774
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Expansin EXPA9'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
5AL
5BL
5DL
Clone Library
Wheat 5-15 DAP spike cDNA library
Tissue
Spike
Developmental Stage
Adult plant
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE0945_G01_M01ZS Wheat 5-15 DAP spike cDNA library Triticum aestivum cDNA clone WHE0945_G01_M01, mRNA sequence.
Other Name
WHE0945_G01_M01ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA018E1X
Clone
WHE0945_G01_M01
Probe
WHE0945_G01_M01
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.5046.1.S1_at505WHE2AFFY
[ Show all 15 ]
DNA
gggtacggggtgaacaacgcggcgctgagcacggcgctgttcaacgaggg
gcagaggtgcggcgcctgcttcgagatccggtgcgagaaccagcctgggt
gggcgtggtgcctcccggggaggccgtccatcgtcgtcaccgccaccaac
ttctgcccgcccaactacgcgctcccctccgacgacggcggctggtgcaa
cccgccccgcccccacttcgacctcgccatgcccatgttcctccacatgg
cgcagtaccgcgccggcatcgtccccgtctcctaccgccgggtggcgtgc
cgga

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