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GrainGenes Sequence Report: CD373674

Sequence	CD373674
Contig	Ta.10.1.S1_a_at Ta.10.2.S1_x_at NSFT03P2_Contig18622
External Databases	Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index	TC308823
wEST map position	CD373674
NCBI UniGene	Ta.10
DB Remark	Locus Source: Triticum aestivum (bread wheat) UniGene title 'Beta glucanase'
Keyword	EST
Species	Triticum aestivum
Cultivar	Chinese Spring
Chromosome	1BL 1DL 7BS
Clone Library	CS wheat etiolated seedling root cDNA library
Tissue	Root
Developmental Stage	Five day old etiolated seedling
Data Source	genbank Release 136, Jun 15 2003 genbank Updated Nov 2006
Title	WHE1209_D05_G09ZT CS wheat etiolated seedling root cDNA library Triticum aestivum cDNA clone WHE1209_D05_G09, mRNA sequence.
Strain	lab_host E. coli SOLR
Clone	WHE1209_D05_G09
Probe	WHE1209_D05_G09
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	tttttttttttttttttttagttctacttacgcacacatgtctgtgcgta tcaaatgcatgatgaatcgacgaagggagagcgtttacatctgctcccct tccatcgtaaatcatacacatacactactacagcaaaccactgctatcgc gtacgcgtctgagctgcctcagcggtcgcaccccaacccgagccctgtac aatacataatgtgcacatacgtacggcatacacgctcttatacgcgtgta cgcgcgcgtacgtacggacatacggacactagctagctacgtacgcagct agctcattcagaagctaatggggtagacgtgctgcatgttggggtagaag agtccccagttctgctccacgccgctgtccttctggttctcgttgaacat ggagaagacgtaggtctcgatggcgccagggtggcggggggtgccgcgcc cgacgtggttgatgaggtactggttgtagatcctggcgttcgccggggtc gccgccgtgccgccgcccgacggccacccgctctccgacaccaccagctt cacgttggagccgccgtgcttggccatggccgtgtagaaggcgtccacgg tggtgtcgaacaggttctggtacccgtaggagccgtcctggaccacggtg ccggacgcggtgaagagcgcgtagctcatgtccatggcgctcgggttgt

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