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GrainGenes Sequence Report: Ta.681.1.S1_x_at

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Sequence
BG313919
Contig
Ta.681.1.S1_at
Ta.681.1.S1_x_at
Ta.681.2.S1_a_at
NSFT03P2_Contig17434
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC283801
NCBI UniGene
Ta.54292
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Ferritin 1A'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Clone Library
Wheat salt-stressed sheath cDNA library
Tissue
Sheath
Developmental Stage
Adult plant
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE2066_G05_N10ZS Wheat salt-stressed sheath cDNA library Triticum aestivum cDNA clone WHE2066_G05_N10, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE2066_G05_N10
Probe
[Wcl12ct69cn118]
{SpCl-555}
BG313919
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 under hydroponic conditions at UC Davis, salt stressed for 12 hours, and for 7 days, then dissected and frozen (Akhunov in J Dvorak Lab). Total RNA was prepared from sheath tissue, equal quantities of RNA were pooled from the two samples, polyA was purified from the pooled RNA, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab at the University of California, Riverside (Akhunov, Chin , Choi, Close, Fenton, Kianian, Otto, Simons, Zhang). 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 under hydroponic conditions at UC Davis, salt stressed for 12 hours, and for 7 days, then dissected and frozen (Akhunov in J Dvorak Lab). Total RNA was prepared from sheath tissue, equal quantities of RNA were pooled from the two samples, polyA was purified from the pooled RNA, a cDNA library was made, and the cDNA clones were in vivo excised to give pBluescript phagemids in the TJ Close lab at the University of California, Riverside (Akhunov, Chin, Choi, Close, Fenton, Kianian, Otto, Simons, Zhang). Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA
gcaagcgcgccgccgccgttcgggttcgagatgttgcctagggttgcgcc
gtctccggccaccgccgccgccgccgccgcagcggttggccagctctccg
gggcggggctcaccgccggttcggtgaggctgccgggggccctgccgtct
gcggcagggtcggcggtctgctgcagggccgcggcgaaggggaaggaggt
gctcagcggcgtgatgttccagccgttcgaggagctcaagggggagctgt
ccctcgtgccgcagggcaaggaccagtcgctcgccaggcacaagttcgtc
gacgagtgcgaggccgccctcaacgagcagatcaatgtggagtataatgc
ctcgtacgcgtatcactccctcttcgcctacttcgaccgcgacaacgttg
ctctcaagggatttgccaagttcttcaaggaatca

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