GrainGenes Sequence Report: BQ160767
Sequence
BQ160767
Contig
NSFT03P2_Contig12017
External Databases
Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index
TC309882
wEST map position
BQ160767
NCBI UniGene
Ta.1358
DB Remark
Locus Source: Triticum aestivum (bread wheat) UniGene title 'Clone wlm1.pk0015.c4:fis, full insert mRNA sequence'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1DS
Clone Library
Wheat unstressed seedling shoot cDNA library
Tissue
Etiolated shoot
Developmental Stage
Five day old seedling
Data Source
genbank Release 135, Apr 15 2003 genbank Updated Nov 2006
Title
WHE0326_C03_E06ZT Wheat unstressed seedling shoot cDNA library Triticum aestivum cDNA clone WHE0326_C03_E06, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE0326_C03_E06
Probe
WHE0326_C03_E06
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. Shoots were harvested. 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. Shoots were harvested. 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
ttttttttttttttttttttttggagtcttcaacctgcaaattcttttca
gacatcatcctgctgaactgagcagtcttaaaatacatcgcggcgacaac
gccgattatttgaagaaccctggctagacttacaactcaataggtgaaac
aacaaagaaatgaaggcaacaagaaccaaatcaccaagaatttctcccgt
gtcaggtctgtagatcatcttagcaattccatcgccttcattttctgcca
aagcttttgtgttggccttaaaactggtcttaacaacacttacctcaaat
ccttcgttgtcagccttttctctggcttgtggctctgtcagcccaaccat
actgatttctggatgagtgaaacaagcggctgggatgcttaaatggttta
gaatgtggtccctcccagagatttgctcaacgactgagattccctgtgca
ctggcagcatgggcaagcatgagtttaccattcgcatctccaatgcaaaa
taaattcggcaccacattgccatcagcatccgtgacttgcatccgctcat
caacaggaataaaaccacgctgtgtaacaacattaatattttccaagcca
agtccgttggtgct

GrainGenes is a product of the Agricultural Research Service of the US Department of Agriculture.
GrainGenes Sequence Report: BQ160767
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