LOCUS BM202328 491 bp mRNA linear EST 16-DEC-2010
DEFINITION C0237F08-3 NIA Mouse 7.5-dpc Whole Embryo cDNA Library (Long) Mus
musculus cDNA clone NIA:C0237F08 IMAGE:30014179 3', mRNA sequence.
ACCESSION BM202328
VERSION BM202328.2
DBLINK BioSample: SAMN00169965
KEYWORDS EST.
SOURCE Mus musculus (house mouse)
ORGANISM Mus musculus
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha;
Muroidea; Muridae; Murinae; Mus; Mus.
REFERENCE 1 (bases 1 to 491)
AUTHORS Piao,Y., Ko,N.T., Lim,M.K. and Ko,M.S.H.
TITLE Construction of long-transcript enriched cDNA libraries from
submicrogram amounts of total RNAs by a universal PCR amplification
method
JOURNAL Genome Res. 11 (9), 1553-1558 (2001)
PUBMED 11544199
COMMENT On Dec 14, 2001 this sequence version replaced BM202328.1.
Other_ESTs: C0237F08-5N
Contact: Dawood B. Dudekula
Laboratory of Genetics
National Institute on Aging/National Institutes of Health
333 Cassell Drive, Suite 4000, Baltimore, MD 21224-6820, USA
Email: cdna@lgsun.grc.nia.nih.gov
Plate: C0237 row: F column: 08
Seq primer: -21M13 Forward
POLYA=Yes.
FEATURES Location/Qualifiers
source 1..491
/organism="Mus musculus"
/mol_type="mRNA"
/strain="C57BL/6J"
/db_xref="niaEST:C0237F08-3"
/db_xref="taxon:10090"
/clone="NIA:C0237F08 IMAGE:30014179"
/tissue_type="whole embryo including extraembryonic
tissues at 7.5-days postcoitum"
/clone_lib="SAMN00169965 NIA Mouse 7.5-dpc Whole Embryo
cDNA Library (Long)"
/dev_stage="7.5-days postcoitum"
/lab_host="DH10B"
/note="Vector: pSPORT1 (Invitrogen); Site_1: SalI; Site_2:
NotI; Mouse cDNA project by the Laboratory of Genetics,
National Institute on Aging (NIA), Intramural Research
Program, NIH (http://lgsun.grc.nia.nih.gov/cDNA). This is
a long-transcript enriched cDNA library (Ref. Genome Res.
11: 1553-1558 (2001). [PMID: 11544199]). Total RNAs were
extracted from a pool of four embryos at 7.5-days
postcoitum. Double-stranded cDNAs were synthesized with an
Oligo(dT) primer [Invitrogen:
5'-pGACTAGTTCTAGATCGCGAGCGGCCGCCCTTTTTTTTTTTTTTT-3'] from
7 ug of total RNA, treated with T4 DNA polymerase, and
purified by ethanol-precipitation. The cDNAs were ligated
to Lone-linker LL-Sal4, purified by phenol/chloroform, and
separated from free linkers by Centricon 100. Then, the
cDNAs were amplified by long-range high fidelity PCR using
Ex Taq polymerase (Takara) with a primer Sal4-S. The
products were purified by phenol/chloroform and Centricon
100. The cDNAs were digested with SalI and NotI enzymes
and cloned into SalI/NotI site of pSPORT1 plasmid vector.
The DH10B E. coli host was transformed with the ligation
mixture by the standard chemical method. The average
insert size is about 2.2 kb. The library was constructed
by Yulan Piao (NIA)."
BASE COUNT 191 a 81 c 71 g 148 t
ORIGIN
1 agaaaaagga aagctgattt ttattttatc aacagccatt cttaaacatg aacatgcata
61 cgtaatattc tacgcacaca tcacagtttt taacgttagt taataatgtt aaacacacaa
121 catacaacct taaaaaaaaa gtcaacctgc aaacttaaaa ctttaaacaa agtcttacta
181 atttaaaaaa ggttttgtgt tgggtaccat ttgtacaaca cagttaattt aaacatttcc
241 attttggctg cacatgaaaa agcggcagta gaaaataaat ttatgagggt tttaaatagc
301 agaataggca gtttcgccat gcaggagaag caatattaaa tattagtttt caaaaaaaat
361 ccacatttaa aaatatttag ttcaagtcac agaacttttc tcagtagaga cctcaatgca
421 atgcgtaatt agctgcctta gatggcctgt tttgaaagga caaaatccct ttcaaagtat
481 aactttactg a
//