Nucleic acid encoding melanoma differentiation associated gene-9
AssigneeThe Trustees of Columbia University in the City of New York
InventorPaul B. Fisher
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AssigneeThe Trustees of Columbia University in the City of New York
InventorPaul B. Fisher
Estimating the term…
This invention provides a method for producing a temporally paced subtracted cDNA library comprising: a) isolating temporally spaced RNAs from cells; b) generating cDNA inserts from the RNAs isolated from step (a); c) producing a temporally spaced cDNA library having clones containing the cDNA inserts generated from step (b); d) producing double stranded cDNA inserts from the temporally spaced cDNA library; e) denaturing the double stranded cDNA inserts; f)contacting the denatured double stranded cDNA inserts produced in step (e) with single-stranded DNAs from another cDNA library under conditions permitting hybridization of the single-stranded DNAs and the double-stranded cDNA inserts; g) separating the hybridized cDNA inserts from the unhybridized inserts; h) generating a cDNA library of the unhybridized inserts, thereby generating a temporally spaced subtracted cDNA library.
An isolated mda-9 gene having the nucleotide sequence shown in SEQ ID NO:1.
An antisense oligonucleotide that specifically hybridizes to an mRNA encoded by the protein-coding region of a gene encoding SEQ ID NO:2.
An isolated nucleic acid molecule comprising a nucleotide sequence beginning with the Adenine at position 76 and ending with Adenine at position 972 of SEQ ID NO:1.
Dependencies are inferred from the claim text.