U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from Nucleotide

FDR202

Identifiers
BioSample: SAMN00152550; EST: LIBEST_020772
Organism
Danio rerio (zebrafish)
cellular organisms; Eukaryota; Opisthokonta; Metazoa; Eumetazoa; Bilateria; Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi; Euteleostomi; Actinopterygii; Actinopteri; Neopterygii; Teleostei; Osteoglossocephalai; Clupeocephala; Otomorpha; Ostariophysi; Otophysi; Cypriniphysae; Cypriniformes; Cyprinoidei; Danionidae; Danioninae; Danio
Attributes
strainTubingen (TU)
sexFemales only
tissueOvary
development stageAdult fish of 3-4 months old
lab hostEscherichia Top10
tissueOvary
vectorpGIS4b
v_typePlasmid
re_1BseRI
re_2Not I
Description

Priming method: GsuI-d(T) priming ; Priming sequence: 5' -GAGCTAGTTCTGGAG(T)16VN -3' ; Directionally cloned: ; 5' cloning site: NotI site GCGGCCGC ; 5' linker/adaptor sequence: 5' -GGATCCGAC -3' ; 3' cloning site: BseRI ; Insert size range: 2kbp-700bp ; For PCR insert analysis: M13 forward and reverse primers ; Library is not amplified ; Recombinants (inserts): 100% ; Library complexity: 1.6 X 106 cfu ; Full-length construction (method): Ng et al, Nature Method 2005 2(2):105-111 ; The pooled tissue RNA was collected and used to construct full length enriched cDNA library and also served as template to synthesize complex first strand cDNA probe. Two high density colony arrays were made from over 110K cDNA clones and hybridized with the probes. Low abundant clones were selected by the Colony Array Subtractive Hybridization (CASH) analysis as they represented rare expressed clones. The hybridization intensities for all clones span from 0 to 200,000 counts and the low abundant selected clones in this library ranges from 0 to 28,000.

Submission
Genome Institute of Singapore, C. Wei; 2007-01-16
Accession:
SAMN00152550
ID:
152550

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center