GrainGenes Sequence Report: NSFT03P2_Contig15420
Sequence
BE425500
Contig
NSFT03P2_Contig15420
Tracefile
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External Databases
Data at GenBank Data at EMBL Data at DDBJ
TIGR Gene Index
TC331304
NCBI UniGene
Ta.39253
DB Remark
Locus Source: Triticum aestivum (bread wheat) UniGene title 'Ribosomal protein S29'
Keyword
EST
Germplasm
Chinese Spring
Species
Triticum aestivum
Cultivar
Chinese Spring
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
WHE0317_A12_A12ZS Wheat unstressed seedling shoot cDNA library Triticum aestivum cDNA clone WHE0317_A12_A12, mRNA sequence.
Other Name
WHE0317_A12_A12ZS  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli SOLR
DNA Library
TA006E1X
Clone
WHE0317_A12_A12
Probe
[Wcl200ct815cn1238] {SpCl-18} BE425500
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; 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
aaaagtagggtttccagttgcaagccgcgccgccgccgccgccgccatgg
gacactcgaacgtctggaactcgcaccccaagaactacggccccggatcg
agggtttgccgtgtctgcggcaactcgcatggcctgatccgcaagtacgg
gctgatgtgctgcaggcagtgcttccgcagcaacgccaaggacattggct
tcatcaagtaccgttaagaatggaaacctcaaaggaagcaaggactagga
aattatcaacgaactgtggtgcttcatcgaggctgatctttatcctataa
gctatgtaatgaactgctattatgtttgaatcctggtgacaaaaccgtga
aacaaagttagtgactgctgtttgagcatgtgaaaccgataattctgtta
ctcttgtgccattctggttagaaagttgctctgcatccttatattttt

GrainGenes is a product of the Agricultural Research Service of the US Department of Agriculture.
GrainGenes Sequence Report: NSFT03P2_Contig15420
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