IE51894B1 - A method of cleaving double stranded dna - Google Patents

A method of cleaving double stranded dna

Info

Publication number
IE51894B1
IE51894B1 IE657/86A IE65786A IE51894B1 IE 51894 B1 IE51894 B1 IE 51894B1 IE 657/86 A IE657/86 A IE 657/86A IE 65786 A IE65786 A IE 65786A IE 51894 B1 IE51894 B1 IE 51894B1
Authority
IE
Ireland
Prior art keywords
dna
stranded dna
primer
double stranded
stranded
Prior art date
Application number
IE657/86A
Other languages
English (en)
Other versions
IE860657L (en
Original Assignee
Genentech Inc
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 Genentech Inc filed Critical Genentech Inc
Publication of IE860657L publication Critical patent/IE860657L/xx
Publication of IE51894B1 publication Critical patent/IE51894B1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575—Hormones
    • C07K14/61—Growth hormone [GH], i.e. somatotropin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575—Hormones
    • C07K14/655—Somatostatins
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/62—DNA sequences coding for fusion proteins
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/70—Vectors or expression systems specially adapted for E. coli
    • C12N15/71—Expression systems using regulatory sequences derived from the trp-operon
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/26—Preparation of nitrogen-containing carbohydrates
    • C12P19/28—N-glycosides
    • C12P19/30—Nucleotides
    • C12P19/34—Polynucleotides, e.g. nucleic acids, oligoribonucleotides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/02—Fusion polypeptide containing a localisation/targetting motif containing a signal sequence
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/70—Fusion polypeptide containing domain for protein-protein interaction
    • C07K2319/74—Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor
    • C07K2319/75—Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor containing a fusion for activation of a cell surface receptor, e.g. thrombopoeitin, NPY and other peptide hormones

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Microbiology (AREA)
  • Plant Pathology (AREA)
  • Physics & Mathematics (AREA)
  • Endocrinology (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Toxicology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Saccharide Compounds (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Peptides Or Proteins (AREA)
IE657/86A 1980-03-24 1981-03-23 A method of cleaving double stranded dna IE51894B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13329680A 1980-03-24 1980-03-24
IE636/81A IE51892B1 (en) 1980-03-24 1981-03-23 A method of producing a polypeptide product and a plasmidic expression vehicle therefor,a method of creating an expression plasmid,a method of cleaving double stranded dna,and specific plasmids

Publications (2)

Publication Number Publication Date
IE860657L IE860657L (en) 1981-09-24
IE51894B1 true IE51894B1 (en) 1987-04-29

Family

ID=22457906

Family Applications (3)

Application Number Title Priority Date Filing Date
IE636/81A IE51892B1 (en) 1980-03-24 1981-03-23 A method of producing a polypeptide product and a plasmidic expression vehicle therefor,a method of creating an expression plasmid,a method of cleaving double stranded dna,and specific plasmids
IE657/86A IE51894B1 (en) 1980-03-24 1981-03-23 A method of cleaving double stranded dna
IE656/86A IE51893B1 (en) 1980-03-24 1981-03-23 A method of creating an expression plasmid for the expression of a heterologous gene

Family Applications Before (1)

Application Number Title Priority Date Filing Date
IE636/81A IE51892B1 (en) 1980-03-24 1981-03-23 A method of producing a polypeptide product and a plasmidic expression vehicle therefor,a method of creating an expression plasmid,a method of cleaving double stranded dna,and specific plasmids

Family Applications After (1)

Application Number Title Priority Date Filing Date
IE656/86A IE51893B1 (en) 1980-03-24 1981-03-23 A method of creating an expression plasmid for the expression of a heterologous gene

Country Status (35)

Country Link
US (2) US5888808A (OSRAM)
EP (3) EP0086548B1 (OSRAM)
JP (3) JPH0724582B2 (OSRAM)
KR (2) KR830005351A (OSRAM)
AR (1) AR248050A1 (OSRAM)
AT (3) ATE52802T1 (OSRAM)
AU (3) AU542640B2 (OSRAM)
BG (3) BG46005A3 (OSRAM)
BR (1) BR8101712A (OSRAM)
CA (2) CA1198068A (OSRAM)
CS (3) CS238612B2 (OSRAM)
DD (3) DD203746A5 (OSRAM)
DE (5) DE3176205D1 (OSRAM)
DK (1) DK173085B1 (OSRAM)
DZ (1) DZ278A1 (OSRAM)
ES (3) ES500617A0 (OSRAM)
FI (3) FI810876A7 (OSRAM)
FR (2) FR2480781B1 (OSRAM)
GB (1) GB2073203B (OSRAM)
GR (1) GR74818B (OSRAM)
HU (1) HU195534B (OSRAM)
IE (3) IE51892B1 (OSRAM)
IL (3) IL62460A (OSRAM)
IT (1) IT1144324B (OSRAM)
MX (1) MX7689E (OSRAM)
MY (1) MY8500896A (OSRAM)
NO (3) NO810986L (OSRAM)
NZ (3) NZ207659A (OSRAM)
OA (1) OA06774A (OSRAM)
PH (4) PH17537A (OSRAM)
PL (2) PL147727B1 (OSRAM)
PT (1) PT72716B (OSRAM)
YU (2) YU45534B (OSRAM)
ZA (1) ZA811368B (OSRAM)
ZW (1) ZW5481A1 (OSRAM)

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