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GrainGenes Sequence Report: BE587227

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Sequence
BE587227
Tracefile
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External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
DB Remark
Locus Source: Secale cereale (rye)
Keyword
EST
Germplasm
Blanco
Species
Secale cereale
Cultivar
Blanco
Clone Library
Secale cereale aluminum-stressed root tip cDNA library
Tissue
Root tip
Developmental Stage
Seedling
Data Source
genbankRelease 135, Apr 15 2003
genbankDownloaded 2008-2009
Title
WHE0510_F03_K06ZR Secale cereale aluminum-stressed root tip cDNA library Secale cereale cDNA clone WHE0510_F03_K06, mRNA sequence.
Other Name
WHE0510_F03_K06ZR  [ wEST-mySQL (obsolete) ]
Strain
lab_host E. coli DH12S
DNA Library
SC010XXX
Clone
WHE0510_F03_K06
Probe
SCM46
Remark
DB_xref: taxon:4550
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: M13 reversed primer.
Note: Vector: pSPORT1; Site_1: SalI; Site_2: NotI; Seeds were germinated aseptically on filter paper and transferred to a hydroponic growth system in a growth chamber when the primary root was 1 cm in length. After a 2-day establishment period, seedlings were subjected to a 5 ppm aluminum stress prior to tissue harvest. Plants were grown in an environmental chamber. The tissue, total RNA, and poly(A) RNA were prepared, and a cDNA library was made (Butler and Gustafson) at University of Missouri , Columbia. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors ).
Note: Vector: pSPORT1; Site_1: SalI; Site_2: NotI; Seeds were germinated aseptically on filter paper and transferred to a hydroponic growth system in a growth chamber when the primary root was 1 cm in length. After a 2-day establishment period, seedlings were subjected to a 5 ppm aluminum stress prior to tissue harvest. Plants were grown in an environmental chamber. The tissue, total RNA, and poly(A) RNA were prepared, and a cDNA library was made (Butler and Gustafson) at University of Missouri, Columbia. Plasmid DNA preparations and DNA sequencing were performed in the OD Anderson lab (all other authors).
DNA
ccacgcgtcccccggcgcggcccctgcgccggacggacgagaagatgacg
acgccgatggcaccgcagcagcagcggacatcgatgaaatcgaggagcag
gatgctgaaatcactgacgacgtcgacgatgaggaggaggaggaggagga
cgacgggttctgcatggtgcagggcatcaccatcgcgctcgagttctccg
acggggaggaggactggatcgtggtctgatcggatctcattcatttgcaa
ataaaccattcaagagaggtcagccgttcacatcaccctgcctctgctgc
tgcgcaattccctgttaattgaaggtcgtgcccccgtgtgtatactgctc
tgttcctcatcctgttaattggtcgtgtccctgtgtatatatatccggtc
accgtctgtctaattgtgtccaattcatggattatcatggcctgaattta
tcaatcgtgtgtgaataaaattaatgaagaagggactcattcctcttcaa
accctgtttctttctaattgattgattgaatggatact

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