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GrainGenes Sequence Report: BG301232

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Sequence
BG301232
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC154429
NCBI UniGene
Hv.23299
DB Remark
Locus Source: Hordeum vulgare subsp. vulgare
UniGene title 'CDNA clone: FLbaf86n19, mRNA sequence'
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
HVSMEb0020B07f Hordeum vulgare seedling shoot EST library HVcDNA0002 (Dehydration stress) Hordeum vulgare subsp. vulgare cDNA clone HVSMEb0020B07f, mRNA sequence.
Strain
lab_host TJC121
vulgare
Clone
HVSMEb0020B07f
Probe
[Bcl698ct1201cn4503]
{SpCl-96}
Remark
DB_xref: taxon:112509
Feature: source: mol_type = 'mRNA';
Locus Comment: 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 = 523; Seq primer: AATTAACCCTCACTAAAGGG; High quality sequence stop: 664.
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
cagcggacggaagcacgcaggcgagcagctctccagcgactcggcgaggg
tggaaatgctcttcagcagcctgttctgtgactcagcgtcatcggagaac
ttttctggccatcccggtgttgagagatgcccattcctgaggaacatcaa
tggagccacaaccttttcattttcttctgctttgcctgtagctgcccggg
gaggcaagggtccgatctttgaggatggaccaggctttgagtcggcattc
aagcttttccatggacaggatgggatagtccccctttcaggaagatcata
tgtgcctgatgagaaccgcagtgagagcactgatgtcaagcctgaacctg
ctctgccctttaatccattggctgctagagccgctaccataagtctatca
tcatttggaccatttgggttcaacttctttaatggcaagggcaaaaagca
gaacaagaagcccaacaatctagaccagtcacacaagaagcccaacaagc
caaatcagaattccatgaaacaaaaaggaggcaacccaccgtcccacgag
gcaatgagcgatgaatggctagaaaatggacagtgcccactcgctcgggc
ttaccgggcaatgagtggtgttctgccccttgtcgcgaaggcactacagc
caccagctggtatgaagctgaagtgccggcctgccattgttgctgcacga
gcagncctcgcacgcccaaccctcgtgaagtccgtccgtgcacagcccct
acctgcaaagatggtagccattgcaatgcttcggatggcaacaaacagtc
ctctcgggtgtggcggagcaccccaaaaaatcttcccccaggggtcgcaa
cgttcaggccgccgttccgtcatcgggagctggggagtcctcaacttccc

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