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Extract from the Register of European Patents

EP About this file: EP1432797

EP1432797 - METHODS FOR DNA MANIPULATION [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  21.09.2007
Database last updated on 24.01.2025
Most recent event   Tooltip21.09.2007Application deemed to be withdrawnpublished on 24.10.2007  [2007/43]
Applicant(s)For all designated states
Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.
Hofgartenstrasse 8
80539 München / DE
[N/P]
Former [2004/27]For all designated states
Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.
Hofgartenstrasse 8
80539 München / DE
Inventor(s)01 / RUDEL, Thomas
Breddiner Weg 5
13591 Berlin / DE
02 / MACHUY, Nikolaus
Paul-Robeson-Str. 12
10439 Berlin / DE
 [2006/16]
Former [2004/27]01 / RUDEL, Thomas
Breddiner Weg 5
13591 Berlin / DE
02 / MACHUY, Nikolaus
Otto-Suhr-Allee 104
10585 Berlin / DE
Representative(s)Weiss, Wolfgang, et al
Weickmann & Weickmann
Patent- und Rechtsanwälte PartmbB
Postfach 860 820
81635 München / DE
[N/P]
Former [2004/27]Weiss, Wolfgang, Dipl.-Chem. Dr., et al
Weickmann & Weickmann Patentanwälte Postfach 86 08 20
81635 München / DE
Application number, filing date02779456.902.10.2002
[2004/27]
WO2002EP11086
Priority number, dateDE200114860702.10.2001         Original published format: DE 10148607
[2004/27]
Filing languageDE
Procedural languageDE
PublicationType: A2 Application without search report
No.:WO03031616
Date:17.04.2003
Language:DE
[2003/16]
Type: A2 Application without search report 
No.:EP1432797
Date:30.06.2004
Language:DE
The application published by WIPO in one of the EPO official languages on 17.04.2003 takes the place of the publication of the European patent application.
[2004/27]
Search report(s)International search report - published on:EP11.12.2003
ClassificationIPC:C12N15/10, C12N15/66
[2005/20]
CPC:
C12N15/66 (EP,US); C12N15/102 (EP,US)
Former IPC [2004/27]C12N15/10
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   IE,   IT,   LI,   LU,   MC,   NL,   PT,   SE,   SK,   TR [2004/27]
Extension statesALNot yet paid
LTNot yet paid
LVNot yet paid
MKNot yet paid
RONot yet paid
SINot yet paid
TitleGerman:METHODEN ZUR DNA-MUTAGENESE UND DNA-KLONIERUNG[2004/27]
English:METHODS FOR DNA MANIPULATION[2004/27]
French:PROCEDES DE MANIPULATION D'ADN[2004/27]
Entry into regional phase26.04.2004National basic fee paid 
26.04.2004Designation fee(s) paid 
26.04.2004Examination fee paid 
Examination procedure02.05.2003Request for preliminary examination filed
International Preliminary Examining Authority: EP
26.04.2004Amendment by applicant (claims and/or description)
26.04.2004Examination requested  [2004/27]
25.04.2005Despatch of a communication from the examining division (Time limit: M04)
11.08.2005Reply to a communication from the examining division
28.11.2005Despatch of a communication from the examining division (Time limit: M04)
31.03.2006Reply to a communication from the examining division
03.05.2007Application deemed to be withdrawn, date of legal effect  [2007/43]
06.06.2007Despatch of communication that the application is deemed to be withdrawn, reason: renewal fee not paid in time  [2007/43]
Fees paidRenewal fee
30.09.2004Renewal fee patent year 03
31.10.2005Renewal fee patent year 04
Penalty fee
Additional fee for renewal fee
31.10.200605   M06   Not yet paid
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Patent Court		 See the Register of the Unified Patent Court for opt-out data
Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Cited inInternational search[XY]  - COONEY AUSTIN J, "Use of T4 DNA polymerase to create cohesive termini in PCR products for subcloning and site-directed mutagenesis.", BIOTECHNIQUES, (199801), vol. 24, no. 1, ISSN 0736-6205, pages 30 - 34, XP001109627 [X] 7 * figure 1 * [Y] 1-6
 [Y]  - FISHER CONSTANCE L ET AL, "Modification of a PCR-based site-directed mutagenesis method", BIOTECHNIQUES, EATON PUBLISHING, NATICK, US, (1997), vol. 23, no. 4, ISSN 0736-6205, pages 570 - 571,574, XP002145359 [Y] 1-6 * figure 1 *
 [A]  - PARIKH ASIT ET AL, "Random mutagenesis by whole-plasmid PCR amplification.", BIOTECHNIQUES, (199803), vol. 24, no. 3, ISSN 0736-6205, pages 428 - 431, XP001109654 [A] 1-7 * figure 1 *
 [A]  - KUIJPER J L ET AL, "FUNCTIONAL CLONING VECTORS FOR USE IN DIRECTIONAL CDNA CLONING USING COHESIVE ENDS PRODUCED WITH T4 DNA POLYMERASE", GENE, ELSEVIER BIOMEDICAL PRESS. AMSTERDAM, NL, (1992), vol. 112, no. 2, ISSN 0378-1119, pages 147 - 155, XP001015913 [A] 1-7 * figures 1,5,6 *

DOI:   http://dx.doi.org/10.1016/0378-1119(92)90370-5
 [A]  - DIETMAIER WOLFGANG ET AL, "DISEC-TRISEC: di- and trinucleotide-sticky-end cloning of PCR-amplified DNA.", NUCLEIC ACIDS RESEARCH, (1993), vol. 21, no. 15, ISSN 0305-1048, pages 3603 - 3604, XP001109679 [A] 1-7 * the whole document *
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.