Clone Dmel\RE35852

General Information
Symbol	Dmel\RE35852	Species	D. melanogaster
Name	RE35852	FlyBase ID	FBcl0194692
Feature type	cDNA_clone	Created / Updated	2005-11-01/2006-08-19
Computed gene(s)	Dmel\Fmr1

Collection Status	BDGP
Known Problems	none
Library	RE
Strain	y; cn bw sp
Tissue Source	embryonic stage whole organism
Vector	pFLC-I
Sequence Data of the Insert
5' Sequence
Total bases	602
GenBank	BI239377
5' sequence data	AGAACGTTGCCGAGCTGCGAAAGTGTGCAAAAGCAAAACGAAGAGAACGC AGCGCAGCCGAAAAAAATTGAAGCAGCACTGCACGCGATATATTTTGTAT TTTCAAAGGTTAAAGCCGCATTCACAGGCATCCGCCGAGGGCAAACGAAG TGCAAAAGTGCCGGCCAGCAGCAACATTTGAAGCAGCAGCCGCCAAGCAA AAGACTGATTTGAGTACAAGGAACTAGAAGCAGGAACGCGAGGTTTCTGC CACTGCACACTGAATTGAGCCCCAGATAACGCGGCAAACTGCAGTCGACG GGGAAAAGTCGGGAGTTGAAGGCTGGGCAGCATCAGCATCAGCAGCAGGA GGGACAGGGACGGACGGCGAAGAACCACCAGAACCAGAACCAAAACAAAG CGGATAAACCAGGAGGCACTACGTCTGGCGATATGGAAGATCTCCTCGTG GAAGTTCGGCTCGACAATGGCGCCTACTACAAGGGCCAGGTGACAGCTGT CGCCGATGATGGCATCTTTGTGGATGTGGACGGTGTGCCCGAAAGTATGA AATATCCATTTGTGAACGTTCGCCTGCCGCCCGAGAAACCGTTGAGGTGG CC
Library Information
Comments	The RE (Riken embryo) library was made from RNA extracted from Drosophila 0-22hr mixed stage isogenic y; cn bw sp strain embryos, polyA+ selected twice, RNA made by Ling Hong. cDNA was synthesized by priming with the oligo(dT) primed adapter (5'-GAGAGAGAGAGGATCCAATACTGGAGAGTTTTTTTTTTTTTTTTVN-3'). The first strand was synthesized in presence of trehalose, which increases the full-length cDNA synthesis (Carninci, P. et. al., PNAS 95: 520-524; Carninci, P. et al., Methods Enzymol. 303: 19-44). Subsequently, full-length cDNA was selected with the biotinylated cap-trapper (Carninci, P. et al., Genomics 37: 327-336). A linker was then ligated to the single-strand cDNA following the published protocol (Shibata, Y., et al., Biotechniques, in press). Subsequently, the cDNA was normalized by using RoT=1.0 as published (Carninci, P., et al., Genome Res. 10: 1617-1630). Second strand cDNA was primed with the (5'-AGAGAGAGAGCTCGAGCTCTAATAAGGTGACACTATAGAACCA-3') primer. After restriction digestion of the hemimethylated cDNA with BamHI and XhoI, the cDNA was cloned in the lambda FLC-I vector. Subsequently, the library was bulk-excised into pFLC-I plasmid as described (Carninci, P., et al., Genomics, 2001, 77:79-90). cDNAs were transformed into DH5-alpha TonA strain.
Library Synonyms
Reported As
Symbol Synonym	RE (Stapleton et al., 2002, )
Library References
Research paper	Stapleton et al., 2002, Genome Res. 12(8): 1294--1300 The Drosophila Gene Collection: identification of putative full-length cDNAs for 70% of D. melanogaster genes. [FBrf0152058]
External Crossreferences & Linkouts
Linkouts
	DGRC - Stock center for Drosophila cDNAs, vectors, and cell lines • FBcl0194692
Synonyms & Secondary IDs ( 0 )
Reported As
Symbol Synonym
Secondary FlyBase IDs

References ( 1 )
Research paper	Stapleton et al., 2002, Genome Res. 12(8): 1294--1300 The Drosophila Gene Collection: identification of putative full-length cDNAs for 70% of D. melanogaster genes. [FBrf0152058]