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GrainGenes Sequence Report: BE405835

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Sequence
BE405835
Contig
Ta.4240.1.S1_at
NSFT03P2_Contig16001
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC296405
wEST map position
BE405835
NCBI UniGene
Ta.4240
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Transcribed locus, moderately similar to NP_001057476.1 Os06g0308800 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
7AS
7BS
7DS
Clone Library
Wheat etiolated seedling root cDNA library
Tissue
Root
Developmental Stage
Five day old etiolated seedling
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE0437_B04_C07ZS Wheat etiolated seedling root cDNA library Triticum aestivum cDNA clone WHE0437_B04_C07, mRNA sequence.
Other Name
WHE0437_B04_C07ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA008E1X
Clone
WHE0437_B04_C07
Probe
WHE0437_B04_C07
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: Strategene 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. 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 Homology
Ta.4240.1.S1_at952WHE2AFFY
Ta.4240.1.S1_at172WHE2AFFY
DNA
accaccaaccaccctacacaattgaaccccagcacacctctcaaaactac
tacgctacagaaaccccacctgctccatacaactaccctaatttccagtc
ttacccgagcttccaggacagcacactaccttctgtcacaacccatcaac
ctgcattccatcctgctagtgatggtggtgtgccaactgctccatcatac
actcctccggcatcaaatcatcctgcaccgacgcagtaccatccgagtgt
tgatgctacacaccaggttacccctcccgctgcgccaccagctagccaat
acgcgtatgacagcaattaccagccggcggtcgagaagatcgctgaggct
cacaaggcagcaagatttgccgtcggcgctcttgcattcgacgacgtgtc
aattgccgtggagcacctgaagcgtgcgctggatctcctgacgaaccctt
ctgcagaaactcactagctgcctggtcctgggagaacacatcttgtgtaa
atacactatactgtaattacgaccaacatggaga

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