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GrainGenes Sequence Report: BF625246

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Sequence
BF625246
External Databases
Data at GenBank
Data at EMBL
Data at DDBJ
TIGR Gene Index
TC188588
NCBI UniGene
Hv.30238
DB Remark
Locus Source: Hordeum vulgare subsp. vulgare
UniGene title 'Transcribed locus, moderately similar to NP_850986.1 ANAC034/ANAC035 (Arabidopsis NAC domain containing protein 34, Arabidopsis NAC domain containing protein 35); transcription factor [Arabidopsis thaliana]'
Keyword
EST
Species
Hordeum vulgare subsp. vulgare
Cultivar
Morex
Clone Library
Hordeum vulgare seedling shoot EST library HVcDNA0001 (Cold stress)
Tissue
Seedling shoot
Data Source
genbankRelease 135, Apr 15 2003
genbankUpdated Nov 2006
Title
HVSMEa0008A15f Hordeum vulgare seedling shoot EST library HVcDNA0001 (Cold stress) Hordeum vulgare subsp. vulgare cDNA clone HVSMEa0008A15f, mRNA sequence.
Strain
lab_host TJC121
vulgare
Clone
HVSMEa0008A15f
Probe
BF625246
Remark
DB_xref: taxon:112509
Feature: source: mol_type = 'mRNA';
Locus Comment: On Dec 18, 2000 this sequence version replaced gi:13082400.; 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 = 583; Seq primer: AATTAACCCTCACTAAAGGG; High quality sequence stop: 691.
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 5oC for 2 days. Shoots were then harvested, total RNA was prepared, poly(A) RNA was purified, one primary unamplified cDNA library was made, and 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:
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 5oC for 2 days. Shoots were then harvested, total RNA was prepared, poly(A) RNA was purified, one primary unamplified cDNA library was made, and 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
ctagctagctagctagctaacacccagctgccctagctcgctagccagca
acctatgcgaattggggaggcggcatgagcagcagatacgagggcggcgc
cgctgcggtggcggcggcgggagctggcgcgggtggcgttaaggagggcg
gcggccgtgacgcgcacgaggacgacctggtgatgccggggttccggttc
cacccgacggaggaggagctcatcgagttctacctccgccgcaaggtgga
gggcaagcgcttcaatgtcgagctcatcaccttcctcgacctctaccgct
acgacccctgggagctcccagcgctggcagcgattggggagaaggagtgg
ttcttctacgtgccgagggaccgcaagtaccggaacggggaccggcccaa
ccgggtgacggcgtcggggtactggaaggcgacgggggcggacaggatga
tccgggcggagagcagccgccccatcgggctcaagaagacgctcgtcttc
tactccggcaaggcgcccaagggcgtccgcagcagctggatcatgaacga
gtaccgnctccccaccgccgacaccgaccgataccacaagacagaaatct
ctctctgccgcgtctacaagcgcaccggcatcgacgacggccgcggccac
ccctcctncgggcggtcgaagatgccctcccgccgcggcgctga

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