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GrainGenes Sequence Report: CD373526

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Sequence
CD373526
Contig
NSFT03P2_Contig10743
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC290445
wEST map position
CD373526
NCBI UniGene
Ta.54383
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Vacuolar proton-inorganic pyrophosphatase'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1BS
[ Show all 6 ]
Clone Library
CS wheat cold-stressed seedling cDNA library
Tissue
Seedling
Developmental Stage
Five-day old seedling
Data Source
genbankRelease 136, Jun 15 2003
genbankUpdated Nov 2006
Title
WHE0370_B03_D06ZT CS wheat cold-stressed seedling cDNA library Triticum aestivum cDNA clone WHE0370_B03_D06, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE0370_B03_D06
Probe
WHE0370_B03_D06
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; This EST was generated by sequencing from the 3' end of the clone.; Sequences have been trimmed to remove vector sequence and low; quality sequence with phred score less than 20.; Seq primer: T7 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
tttttttttttttttttgaggcaacaatcgtcatgatatcatcgttcaag
ggttcaaacattatcgtcgtcatcatgggacgaggaaaatttgccagaca
cataccaataatgaccgaggacatccggtctctctcttctactacataga
gctacaagccggtaatggtgagactaacgtaacacacccaagaggccaaa
gggaaagtggggggtaaactgcggcaatcctggaataatgacacgagaac
caaaaataacagcagcgcacaacatacgaacggcgggcgggcggggcaaa
gttattcgtgatggtgatggtgtccgtaaattccaagtccgctcaacgag
tcttctagatgtacttgaacagcacacctccatacgtggcgaaaaagggc
gcgaacacgagggactcgacggccatgagcttgatgaggatgttgagcga
cgggcctgaggtgtccttgagggggtctccgatggtgtcgccgatcacgg
cgg

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