GrainGenes Sequence Report: Ta.13546.1.A1_at
Sequence
BQ162396
Contig
Ta.13546.1.A1_at
External Databases
Data at GenBank Data at EMBL Data at DDBJ
wEST map position
BQ162396
NCBI UniGene
Ta.38869
DB Remark
Locus Source: Triticum aestivum (bread wheat) UniGene title 'Transcribed locus, strongly similar to NP_001064791.1 Os10g0464000 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
1DL
Clone Library
Wheat etiolated seedling root cDNA library
Tissue
Root
Developmental Stage
Five day old etiolated seedling
Data Source
genbank Release 135, Apr 15 2003 genbank Updated Nov 2006
Title
WHE1210_H11_O22ZT Wheat etiolated seedling root cDNA library Triticum aestivum cDNA clone WHE1210_H11_O22, mRNA sequence.
Strain
lab_host E. coli SOLR
Clone
WHE1210_H11_O22
Probe
WHE1210_H11_O22
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. Roots 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. Roots 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
ttttttttttttttttttattaaatttaaagaagatgtggaaacattatt
ttctcagaagctcaagtatagccacacaacaaccattcaatacatccatc
ttaagtccccatgctccattttgtatatatttaggcacttatctacggat
atctaaggactagctgatacattataaaatacaaaccattttacaagctt
ctgtagatatctcacaagtcacaaactcacacaatattatcacgcgccta
aaggaccattttcttatgtcaaaccaggagcctgtaggactgacctcacc
aattcaaattcttgtacacatgggttcagttcaggcattatgtgtggacg
cctgaagaatccattgcgaatctgactggcaatgtctgcaacagcacctg
ggccatgcgggatgaaaactgc
GrainGenes is a product of the Agricultural Research Service of the US Department of Agriculture.
GrainGenes Sequence Report: Ta.13546.1.A1_at
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GrainGenes is a product of the Agricultural Research Service of the US Department of Agriculture. | |||