DE20210018U1 - Chemical composition for the production of nucleic acid chips - Google Patents

Chemical composition for the production of nucleic acid chips

Info

Publication number
DE20210018U1
DE20210018U1 DE20210018U DE20210018U DE20210018U1 DE 20210018 U1 DE20210018 U1 DE 20210018U1 DE 20210018 U DE20210018 U DE 20210018U DE 20210018 U DE20210018 U DE 20210018U DE 20210018 U1 DE20210018 U1 DE 20210018U1
Authority
DE
Germany
Prior art keywords
chemical composition
composition according
substituted
unsubstituted
condensed
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
DE20210018U
Other languages
German (de)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Universitaet Konstanz
Original Assignee
Universitaet Konstanz
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Universitaet Konstanz filed Critical Universitaet Konstanz
Priority to DE20210018U priority Critical patent/DE20210018U1/en
Priority claimed from DE10209203A external-priority patent/DE10209203A1/en
Publication of DE20210018U1 publication Critical patent/DE20210018U1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/00497Features relating to the solid phase supports
    • B01J2219/00527Sheets
    • B01J2219/00529DNA chips
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583Features relative to the processes being carried out
    • B01J2219/00603Making arrays on substantially continuous surfaces
    • B01J2219/00605Making arrays on substantially continuous surfaces the compounds being directly bound or immobilised to solid supports
    • B01J2219/00608DNA chips
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583Features relative to the processes being carried out
    • B01J2219/00603Making arrays on substantially continuous surfaces
    • B01J2219/00605Making arrays on substantially continuous surfaces the compounds being directly bound or immobilised to solid supports
    • B01J2219/00614Delimitation of the attachment areas
    • B01J2219/00617Delimitation of the attachment areas by chemical means
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583Features relative to the processes being carried out
    • B01J2219/00603Making arrays on substantially continuous surfaces
    • B01J2219/00605Making arrays on substantially continuous surfaces the compounds being directly bound or immobilised to solid supports
    • B01J2219/00623Immobilisation or binding
    • B01J2219/00626Covalent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583Features relative to the processes being carried out
    • B01J2219/00603Making arrays on substantially continuous surfaces
    • B01J2219/00659Two-dimensional arrays
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583Features relative to the processes being carried out
    • B01J2219/00603Making arrays on substantially continuous surfaces
    • B01J2219/00677Ex-situ synthesis followed by deposition on the substrate
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00709Type of synthesis
    • B01J2219/00711Light-directed synthesis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/11Compounds covalently bound to a solid support
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B40/00Libraries per se, e.g. arrays, mixtures

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Nanotechnology (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Composite Materials (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biotechnology (AREA)
  • Electroluminescent Light Sources (AREA)

Description

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically  

Der Beschreibungstext wurde nicht elektronisch erfaßtThe description text was not recorded electronically

Claims (9)

1. Chemische Zusammensetzung umfassend ein Molekül mit einer labilen funktionellen Gruppe sowie eine chemische Verbindung, deren Triplettzustand energetisch höher oder sehr ähnlich liegt wie der Triplettzustand der labilen funktionellen Gruppe.1. Chemical composition comprising a molecule with an unstable functional Group as well as a chemical compound, the triplet state of which is energetically higher or is very similar to the triplet state of the labile functional group. 2. Chemische Zusammensetzung nach Anspruch 1, dadurch gekennzeichnet, dass die labile funktionelle Gruppe eine photolabile Gruppe ist.2. Chemical composition according to claim 1, characterized in that the labile functional group is a photolabile group. 3. Chemische Zusammensetzung nach Anspruch 2, dadurch gekennzeichnet, dass der Singulettzustand der chemischen Verbindung energetisch gleich hoch oder tiefer liegt als der Singulettzustand der photolabilen Gruppe.3. Chemical composition according to claim 2, characterized in that the The singlet state of the chemical compound is energetically equal to or lower than the singlet state of the photolabile group. 4. Chemische Zusammensetzung nach Anspruch 3, dadurch gekennzeichnet, dass die Triplett-Singulett Energielücke der chemischen Verbindung kleiner ist als die Triplett- Singulett Energielücke der photolabilen Gruppe.4. Chemical composition according to claim 3, characterized in that the Triplet singlet energy gap of the chemical compound is smaller than the triplet Singlet energy gap of the photolabile group. 5. Chemische Zusammensetzung nach Anspruch 1 oder 4, dadurch gekennzeichnet, dass die photolabile Gruppe ausgewählt ist aus der Gruppe bestehend aus NPPOC, MeNPOC, NPES, NPPS, MeNPPOC, DMBOC und deren substituierten Derivaten, substituierten und unsubstituierten, kondensierten und nichtkondensierten 2- (Nitroaryl)ethoxycarbonyl oder -thiocarbonyl-Verbindungen, substituierten und unsubstituierten, kondensierten und nichtkondensierten 2-Nitrobenzyl-, 2- Nitrobenzyloxycarbonyl bzw. thiocarbonyl Verbindungen, substituierten und unsubstituierten, kondensierten und nichtkondensierten 2- (Nitroheterocycloaryl)ethoxycarbonyl, oder -thiocarbonyl Verbindungen, sowie substituierten und unsubstituierten, kondensierten und nichtkondensierten 2- (Nitroheterocycloalkyl)ethoxy-carbonyl/thiocarbonyl Verbindungen, substituierten und unsubstituierten 2-Nitro-N-Methylanilincarbonyl- bzw. thiocarbonylderivaten. 5. Chemical composition according to claim 1 or 4, characterized in that the photolabile group is selected from the group consisting of NPPOC, MeNPOC, NPES, NPPS, MeNPPOC, DMBOC and their substituted derivatives, substituted and unsubstituted, condensed and uncondensed 2- (Nitroaryl) ethoxycarbonyl or thiocarbonyl compounds, substituted and unsubstituted, condensed and uncondensed 2-nitrobenzyl, 2- Nitrobenzyloxycarbonyl or thiocarbonyl compounds, substituted and unsubstituted, condensed and uncondensed 2- (Nitroheterocycloaryl) ethoxycarbonyl, or -thiocarbonyl compounds, as well substituted and unsubstituted, condensed and uncondensed 2- (Nitroheterocycloalkyl) ethoxy-carbonyl / thiocarbonyl compounds, substituted and unsubstituted 2-nitro-N-methylaniline carbonyl or thiocarbonyl derivatives.   6. Chemische Zusammensetzung nach Anspruch 1 oder 4, dadurch gekennzeichnet, dass die chemische Verbindung das Strukturmotiv
aufweist, wobei Y = O, S, N, Se oder Te ist, n = 1 oder 2 bedeutet, C Bestandteil eines aromatischen, heteroaromatischen oder kondensierten aromatischen oder heteroaromatischen Systems ist und wobei im Falle, dass n = 2 ist, das aromatische, heteroaromatische oder kondensierte aromatische oder heteroaromatische System gleich oder verschieden sein kann.
6. Chemical composition according to claim 1 or 4, characterized in that the chemical compound has the structural motif
, where Y = O, S, N, Se or Te, n = 1 or 2, C is part of an aromatic, heteroaromatic or condensed aromatic or heteroaromatic system and where, if n = 2, the aromatic, heteroaromatic or fused aromatic or heteroaromatic system may be the same or different.
7. Verwendung einer chemischen Zusammensetzung nach einem der vorhergehenden Ansprüche 1 bis 6 zur Herstellung von DNA-Chips.7. Use of a chemical composition according to one of the preceding Claims 1 to 6 for the production of DNA chips. 8. Kit umfassend eine chemische Zusammensetzung nach einem der Ansprüche 1 bis 6.8. Kit comprising a chemical composition according to any one of claims 1 to 6. 9. Kit, der einen Teil oder alle Reagenzien und/oder Hilfsstoffe und/oder Lösungsmittel und/oder eine Arbeitsanweisung zur Durchführung eines Verfahrens zur Abspaltung labiler funktioneller Gruppen aus Molekülen durch Einwirkung elektromagnetischer Strahlung und/oder zur Herstellung von DNA-Chips enthält.9. Kit containing some or all of the reagents and / or excipients and / or solvents and / or work instructions for performing a spin-off process labile functional groups of molecules by the action of electromagnetic Contains radiation and / or for the production of DNA chips.
DE20210018U 2002-03-04 2002-03-04 Chemical composition for the production of nucleic acid chips Expired - Lifetime DE20210018U1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE20210018U DE20210018U1 (en) 2002-03-04 2002-03-04 Chemical composition for the production of nucleic acid chips

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10209203A DE10209203A1 (en) 2002-03-04 2002-03-04 Composition useful for preparing DNA chips comprises compound with labile functional group and a sensitizer that acts by triplet-triplet energy transfer
DE20210018U DE20210018U1 (en) 2002-03-04 2002-03-04 Chemical composition for the production of nucleic acid chips

Publications (1)

Publication Number Publication Date
DE20210018U1 true DE20210018U1 (en) 2002-11-28

Family

ID=26011046

Family Applications (1)

Application Number Title Priority Date Filing Date
DE20210018U Expired - Lifetime DE20210018U1 (en) 2002-03-04 2002-03-04 Chemical composition for the production of nucleic acid chips

Country Status (1)

Country Link
DE (1) DE20210018U1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10237704A1 (en) * 2002-08-09 2004-03-11 Chemogenix Gmbh Method and device for the intermolecular transfer of activation energy for bond cleavage through space
DE102004019098A1 (en) * 2004-04-20 2005-11-10 Chemogenix Gmbh Photolabile protecting groups

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10237704A1 (en) * 2002-08-09 2004-03-11 Chemogenix Gmbh Method and device for the intermolecular transfer of activation energy for bond cleavage through space
DE102004019098A1 (en) * 2004-04-20 2005-11-10 Chemogenix Gmbh Photolabile protecting groups
US7432368B2 (en) 2004-04-20 2008-10-07 Roche Nimblegen, Inc. Photolabile protecting groups

Similar Documents

Publication Publication Date Title
DE112012006712B4 (en) Process and system for extracting carbon fibers from a resin composite by solvent cracking
DE69008625T2 (en) Device and method for encrypted security marking for the protection of valuables.
DE3301833A1 (en) METHOD FOR SIMULTANEOUS SYNTHESIS OF SEVERAL OLIGONOCLEOTIDES IN A SOLID PHASE
DE102014101069B4 (en) Metal release additive, composition including the same and method of metal release using the composition
EP0383117A3 (en) Pyridine-substituted esters of acrylic acid
DE2202271A1 (en) Process for joining metals with organic compounds
EP0115038B1 (en) Process for the production of coloured decorative paper with a three-dimensional surface structure
DE20210018U1 (en) Chemical composition for the production of nucleic acid chips
DE2430501A1 (en) PICKLING PROCESS FOR METALLIC OBJECTS
DD247689A5 (en) METHOD FOR PRODUCING COATING POLYMERS WITH INCREASED ELASTICITY
EP0315018A3 (en) Fluoromethoxyphenyl-dihydropyridines, process for their preparation and their use in drugs
DE3330031C2 (en)
DE3726108A1 (en) Process for producing hard fibreboards
DE60218568T2 (en) Thin polymer layer, manufacturing process, binder for bio-chip, bio-chip and process for its production
Gradl Sustainable Research based on Recovered Active Pharmaceutical Ingredients
DE1032209B (en) Breathable synthetic leather on a polyvinyl chloride basis with a dirt-repellent surface
EP0356796A3 (en) Aminomethyl peptides, production process and their use as medicaments
DE602004005300T2 (en) Polynucleotides microarray including two or more groups of polynucleotide probes immobilized on a substrate
DE2031234C3 (en) Process for the production of water-repellent, air-permeable synthetic leather
DE2833586C2 (en) Process for deacidification and maintenance of acid-free freedom from certain chlorinated hydrocarbons
DD238395A1 (en) METHOD FOR SELECTIVELY FIXING BIOLOGICAL ACTIVE SUBSTANCES
DE1795828A1 (en) ADENOSINE DERIVATIVES
DE679341C (en) Process for the production of resinous condensation products from nitrogen-containing heterocyclic compounds and low molecular weight aldehydes of the fatty series
DE659594C (en) Process for making soap bars
DE1097669B (en) Process for the production of hardened foams with enlarged surface from aminoplasts

Legal Events

Date Code Title Description
R207 Utility model specification

Effective date: 20030109

R150 Term of protection extended to 6 years

Effective date: 20050615

R151 Term of protection extended to 8 years

Effective date: 20080611

R152 Term of protection extended to 10 years

Effective date: 20100609

R071 Expiry of right
R071 Expiry of right