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GrainGenes Sequence Report: Ta.13966.3.S1_a_at

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Sequence
BE442892
Contig
Ta.13966.1.S1_at
Ta.13966.3.S1_a_at
NSFT03P2_Contig11688
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC307531
wEST map position
BE442892
NCBI UniGene
Ta.13966
DB Remark
Locus Source: Triticum aestivum (bread wheat)
UniGene title 'Transcribed locus, strongly similar to NP_001063096.1 Os09g0394900 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
Chromosome
5AL
5BL
5DL
Clone Library
Wheat etiolated seedling root normalized cDNA library
Tissue
Root
Developmental Stage
Five day old etiolated seedling
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
WHE1107_B01_D01ZS Wheat etiolated seedling root normalized cDNA library Triticum aestivum cDNA clone WHE1107_B01_D01, mRNA sequence.
Other Name
WHE1107_B01_D01ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli DH10B
DNA Library
TA008E3N
Clone
WHE1107_B01_D01
Probe
WHE1107_B01_D01
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 pBluescript SK; 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 in the TJ Close lab (Choi, Close, Fenton) at the University of California, Riverside. The cDNA clones were in vivo excised to give pBluescript phagemids before normalization was carried out. The mass excision of phagemid library and normalization were done in HT Nguyen lab by D. Zhang at Texas Tech Univeristy. Normalization protocol used was that of Soares. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA Homology
Ta.13966.1.S1_at831WHE2AFFY
Ta.13966.1.S1_at620WHE2AFFY
TaAffx.83360.1.S1_at511WHE2AFFY
TaAffx.83360.1.S1_at412WHE2AFFY
Ta.13966.3.S1_a_at174WHE2AFFY
DNA
cttgtaagggttgtggtaacaaggactgagattgatatgcagtatatcaa
ggcagaatattacaagaaatacaaaaagcctttagctgatgctatccatt
ccgaaacatcaggcggttatcggacattcctgctttctctggttggtagc
cattaggctatgtttcctcaccgcacactctgctctgtcgcattacttta
ccctaaaggcctaaacgcagtgactctacctggccaaaatgtatgacgtc
gtcatcactgtgttctggagcttcgctgacaactatttctgctttctctt
ggtttatgcttgcctaaaatgtgtgtatattatttggatccggggactct
agtgcagtggctgctgctggttccatctttcatggcatgtgttatcagtg
cagttggtttgatgattgtatttggctttactgctttcactgaagttcac
actgttatttaactttattgagaaaaaaaaaaaaaaaaaa

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