cDNA Library, Planaria
Cat. No. 02-709
Store at -20°C
Size 500 ng
500 ng (40 ng/ul, 13ul) in 10 mM Tris-HCl-1mM EDTA (pH 7.5)
- Number of independent clones: 14 x 106
- Average insert size : longer than 1 kb
This cDNA library (plasmid DNA) is constructed from Planaria-derived poly(A)+ RNA by the Linker-Primer method (Ref.1) by Professor Hiroshi Nojima of the Research Institute for Microbial Diseases, Osaka University. This library is unidirectionally cloned using the oligo (dT)18 linker primer which contains the restriction enzyme site of Not I, and BamHI (Bgl II)-Sma I adaptor. The pAP3neo vector used in this library can express genes in mammalian cells as it contains the SV40 promoter. It also contains Ori for plasmid replication and f1 ori which is necessary for ssDNA synthesis in E. coli, and bacteriophage T7 and T3 promoter for RNA synthesis (see Figure). GenBank Accession No. AB003468.
PCR screening of known or unknown gene: Prepare the primers for the known or unknown gene (cDNA) and amplify the gene by PCR from this library followed by cloning to an appropriate vector. It is useful for large-scale protein productions, and preparation of probes, etc.
Standard amplifying conditions: 35 cycles of PCR reactions using 10-100 ng of cDNA as a template. (Change the quantity of template and the number of cycles depending on the expression levelof mRNA
of the particular gene.)
* This library is to be used only by the purchaser. It is not allowed to amplify and transfer the library to a third person.
* Related products: human tissue specific cDNA libraries and cDNA libraries of model organisms (See HP).
- Kobori M et al ” Large scale isolation of osteoclast-specific genes by an improved method involving the preparation of a subtracted cDNA library.” Genes Cells 3: 459-475 (1998) PMID: 9753427
- Sambrook J and Russell DW Molecular Cloning Chapter 11 ”Preparation of cDNA libraries and gene identification.” CSHL Press (2001)