GrainGenes Sequence Report: BE471257
Sequence
BE471257
Contig
Ta.27564.1.S1_at Ta.27609.1.S1_s_at NSFT03P2_Contig12787
Tracefile
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External Databases
Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index
TC344828
NCBI UniGene
Ta.48698
DB Remark
Locus Source: Triticum aestivum (bread wheat) UniGene title 'Clone wdk2c.pk013.l7:fis, full insert mRNA sequence'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Clone Library
Wheat drought-stressed seedling cDNA library
Tissue
Seedling without endosperm
Developmental Stage
Five day old seedling
Data Source
genbank Release 135, Apr 15 2003 genbank Updated Nov 2006
Title
WHE0286_A11_B22ZS Wheat drought-stressed seedling cDNA library Triticum aestivum cDNA clone WHE0286_A11_B22, mRNA sequence.
Other Name
WHE0286_A11_B22ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA005E1X
Clone
WHE0286_A11_B22
Probe
MAG1597
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; Seeds were surface-sterilized , germinated and grown aseptically in the dark at room temperature on filter paper with water, nystatin and cefotaxime in covered crystallization dishes. Five-day old seedlings were incubated for one day at 90% RH. After removing endosperm, seedlings were transferred to desiccator jar containing saturated MgSO4 at room temperature for 24 hr. The tissue, 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; Seeds were surface-sterilized, germinated and grown aseptically in the dark at room temperature on filter paper with water, nystatin and cefotaxime in covered crystallization dishes. Five-day old seedlings were incubated for one day at 90% RH. After removing endosperm, seedlings were transferred to desiccator jar containing saturated MgSO4 at room temperature for 24 hr. The tissue, 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
tgtacagcggtccaccatcggcatgtgcctcaccgagacgctcgacgaga
tggtctccagcggcaccctcagccccgagctcgccatccaagtgctagtc
cagttcgataagtctatgacggaggcactggaaaaccaagtgaagagcaa
ggttactgtcaagggccatctgcacacctacaggttctgcgacaacgtgt
ggacattcatattaaccgacgcgcagttcaagaacgaggagacgaccgag
caggtgggcaaggtgaagatcgtggcctgcgactccaagctactcagcca
ataagcagctctcgcgcgagctgccgac

GrainGenes is a product of the Agricultural Research Service of the US Department of Agriculture.
GrainGenes Sequence Report: BE471257
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