mRNA amplification

US7229760B2 · kind B2 · utility

Assignee

• Micromet AG · DE

Inventors

• Dietlind Zohlnhöfer · Birkenfeld, DE
• Christoph Klein · Darmstadt, DE

Key dates

• Filing date: Mar 23, 2001
• Grant date: Jun 12, 2007
• Expiry date: Aug 28, 2022

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C12Q2600/158
• WIPO field: Biotechnology
• WIPO sector: Chemistry

Abstract

The present invention relates to a method for the amplification of mRNA of a sample, comprising the steps of i.) generating cDNA from polyadenylated RNA employing at least one primer hybridizing to said polyadenylated RNA and comprising a 5′ poly(C) or a 5′ poly(G) flank; ii.)(aa) if present, removing non-hybridized, surplus primer(s) and/or surplus dNTPs; ii.)(ab) 3′ tailing of said generated cDNA with a poly(G) tail when in step i.(a) primer(s) comprising a 5′ poly(C) flank was employed or a poly(C) tail when in step i.(a) primer(s) comprising a 5′ poly(G) flank was employed; or ii.)(b) 3′ tailing of said generated cDNA with a poly(G) tail when in step i.(a) primer(s) comprising a 5′ poly(C) flank was employed or a poly(C) tail when in step i.(a) primer(s) comprising a 5′ poly(G) flank was employed using an RNA-ligase, irrespective of the presence or absence of surplus primer(s) and/or surplus dNTPs; and iii.) amplifying the tailed cDNA with a primer hybridizing to the tail(s) generated in step ii(ab) or ii(b). Furthermore, the present invention relates to methods for the preparation of in vitro surrogate(s), for identifying expressed genes in a test sample, for identifying a dru…