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GrainGenes Sequence Report: Ta.1967.2.A1_x_at

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Sequence
BE490728
Contig
Ta.1967.2.A1_x_at
TaAffx.104812.1.S1_s_at
NSFT03P2_Contig15436
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC318873
wEST map position
BE490728
NCBI UniGene
Ta.64879
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Transcribed locus, moderately similar to NP_001067015.1 Os12g0560200 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
5AS
5BS
5DS
7AS
7DS
Clone Library
Wheat cold-stressed seedling cDNA library
Tissue
Seedling
Developmental Stage
Five-day old seedling
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE0369_B09_D17ZS Wheat cold-stressed seedling cDNA library Triticum aestivum cDNA clone WHE0369_B09_D17, mRNA sequence.
Other Name
WHE0369_B09_D17ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA007E1X
Clone
WHE0369_B09_D17
Probe
WHE0369_B09_D17
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 transferred to 5 C cold room and kept for 48 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 transferred to 5 C cold room and kept for 48 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 Homology
TaAffx.104812.1.S1_s_at793WHE2AFFY
TaAffx.104812.1.S1_s_at577WHE2AFFY
Ta.485.1.A1_at80WHE2AFFY
Ta.485.1.A1_at64WHE2AFFY
TaAffx.109337.1.S1_at62WHE2AFFY
DNA
caccccgtctaccgcctgctgcacccgcacttccgcttcaccatggagat
caacgcgcaggcgcgcgcgatgctcatcaacgccgacgggatcatcgagg
gctccttcgcgcccggggagtactccattgagctcagctccgtggcttac
gaccagcagtggcggttcgacatggaggccctgccggaagacctcatccg
gaggggcatggcggtcaggaaggagaatggcgagctggagctggccatag
aggactacccctacgccaacgacggcctgctcatctgggacgccatcaag
gagtgggcgttgacctacgtggagcactactacccgtgcaccgcggacat
cgtcgatgacgaggagctccaggcttggtggaccgaggtgcgcaccaaag
gccacgccgacaagcaggacgagccgtggtggcccgagctggacagccat
gagaacctggcgcaggccctggcgaccatcatgtgggtcacgtcggcgca
tcacg

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