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GrainGenes Sequence Report: BG301284

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Sequence
BG301284
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC166450
NCBI UniGene
Hv.3354
DB Remark
Locus Source: Hordeum vulgare subsp. vulgare
UniGene title 'Transcribed locus, strongly similar to NP_001066312.1 Os12g0180400 [Oryza sativa (japonica cultivar-group)]'
Keyword
EST
Species
Hordeum vulgare subsp. vulgare
Cultivar
Morex
Clone Library
Hordeum vulgare seedling shoot EST library HVcDNA0002 (Dehydration stress)
Tissue
Seedling shoot
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
HVSMEb0020H09f Hordeum vulgare seedling shoot EST library HVcDNA0002 (Dehydration stress) Hordeum vulgare subsp. vulgare cDNA clone HVSMEb0020H09f, mRNA sequence.
Strain
lab_host TJC121
vulgare
Clone
HVSMEb0020H09f
Probe
[Bcl298ct652cn2647]
{SpCl-324}
Remark
DB_xref: taxon:112509
Feature: source: mol_type = 'mRNA';
Locus Comment: On Feb 22, 2001 this sequence version replaced gi:13098811.; Contact: Wing RA; Clemson University Genomics Institute; Clemson University; 100 Jordan Hall, Clemson, SC 29634, USA; Tel: 864 656 7288; Fax: 864 656 4293; Email: rwing@clemson.edu; Total hq bases = 426; Seq primer: AATTAACCCTCACTAAAGGG; High quality sequence stop: 574.
Locus Comment: On Feb 22, 2001 this sequence version replaced gi:13098811.; Contact: Wing RA; Clemson University Genomics Institute; Clemson University; 100 Jordan Hall, Clemson, SC 29634, USA; Tel: 864 656 7288; Fax: 864 656 4293; Email: rwing@clemson.edu; Total hq bases = 426; Seq primer: AATTAACCCTCACTAAAGGG; High quality sequence stop: 573.
Note: Vector: lambdaZAP; Site_1: EcoR1; Site_2: Xho1; Seeds were surface sterilized then germinated under axenic conditions in the dark at room temperature on filter paper with water, nystatin and cefotaxime in covered crystallization dishes. Five-day old seedlings were incubated at 90% RH for 24 hr. Shoots were then harvested, total RNA was prepared, poly(A) RNA was purified, one primary unamplified cDNA library was made, 600000 pfu were in vivo excised to give pBluescript SK(-) cDNA phagemids. These steps were performed in the TJ Close laboratory at the University of California, Riverside (Choi, Close, Fenton). Phagemids were plated and picked at the Clemson University Genomics Institute (CUGI) (Begum, Palmer, Frisch, Atkins and Wing). Plasmid DNA preparations, DNA sequencing and sequence analysis were performed at CUGI (Wing, Yu, Frisch, Henry, Simmons, Oates, Rambo, Main). The sequence has been trimmed to remove vector sequence and contains a minimum of 100 bases of phred value 20 or above. For more details on library preparation and sequence analysis see http:
DNA
accatcgacccttcttcttccccagcggcggctacggcggcggatggaag
atgatcatcccggttcgctgcttcacctgcggcaaggtgatcgggaacaa
gtgggaccactacctcgatcttctccaggctgattacaccgagggggatg
ctctggatgccttgggcttggttcgctactgctgccgccgtatgctcatg
acccatgttgaccttatcgagaagttgctcaactacaacaccctggagaa
gacggagacaagttgaagttaattgaacccatgctgcctggaaacccttg
ttcctttgtactacttttcaagatggatggtatgctgtttcttatgtcag
tgcttatgaggtgcaaagtgtcaggtagtcctgatatgatatgaagttgg
tttgtccatgaatctccaaggactattagtgtgaccatgcgtttctacta
tgtaatcttcacggctattagttaaccaacaaatctaatgcattgtccag
tttcaaacttattatgctccaagtgttgaacatgttatccctgtgtttaa
aaagaaaaagaaaaaagaaaaaa

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