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GrainGenes Sequence Report: NSFT03P2_Contig17475

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Sequence
BE490592
Contig
Ta.1048.1.S1_at
NSFT03P2_Contig17475
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC278151
wEST map position
BE490592
NCBI UniGene
Ta.1048
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Clone wle1n.pk0057.g6:fis, full insert mRNA sequence'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1AL
1BL
1DL
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
WHE0370_G03_N06ZS Wheat cold-stressed seedling cDNA library Triticum aestivum cDNA clone WHE0370_G03_N06, mRNA sequence.
Other Name
WHE0370_G03_N06ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA007E1X
Clone
WHE0370_G03_N06
Probe
WHE0370_G03_N06
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
Ta.1048.1.S1_at954WHE2AFFY
[ Show all 9 ]
DNA
ggcctctgcaccgccatcgccaggcactgccccaacgctctcgtcaatat
gatcagcaaccctgtcaactcgactgtcccaattgcagctgaggtgttca
agaaggctggtacctatgatgagaagaagctgtttggtgtgaccactctt
gatgttgttcgtgctaaaacattctatgctggaaaggcgaacgtgccagt
tactggggtgaatgttcctgttgttggtggccatgctggaatcactatcc
tgccactgttctcgcaggctactcctgcaagtaatgcattgtcccatgag
gaccttgtcgccctcacgaagaggacacaagatggtgggacggaagttgt
tgaagcgaaggctggaaagggctcancaacattgtcgatggcatatgctg
gtgcagtttttggagatgcatgcttgaaggggctcaacggtgttcctgac
attgtagagtgctcttttgtccaatcaaccgtaacagagctgccattctt
tgcctc

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