0000000000319949

AUTHOR

Helmut Reiländer

showing 3 related works from this author

Probing human beta1- and beta2 -adrenoceptors with domain-specific fusion protein antibodies.

1997

In order to generate antibodies suitable for immunological studies on beta-adrenoceptors constitutively expressed at low levels in cells or tissues we have produced fusion proteins of the amino- and carboxy-terminus, and the second extracellular loop of the human beta 1- or beta 2-adrenoceptors with bacterial glutathione-S-transferase in E. coli. Rabbit antibodies raised against these fusion proteins strongly reacted with intact human beta 1- or beta 2-adrenoceptors in a subtype- and domain-specific manner. Antibodies directed against the second extracellular loop of the beta 1-adrenoceptor reacted stronger with non-denatured receptors and decreased the affinity of the 3H-labelled antagonis…

Recombinant Fusion ProteinsBlotting WesternEnzyme-Linked Immunosorbent AssayBiologyImmunofluorescenceProtein Structure SecondaryAntibodiesRadioligand AssayAntibody SpecificitymedicineExtracellularAnimalsHumansAvidityReceptorFluorescent Antibody Technique IndirectPharmacologymedicine.diagnostic_testMolecular biologyFusion proteinPrimary and secondary antibodiesPrecipitin TestsBlotMicroscopy FluorescenceBiochemistrybiology.proteinRabbitsReceptors Adrenergic beta-2AntibodyReceptors Adrenergic beta-1European journal of pharmacology
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A Rapid Method for Amplification of Plastome DNA-Fragments from Spinacia oleracea by PCR

1993

Summary Polymerase Chain Reaction (PCR) was used as a very powerful technique to amplify DNA-fragments. Isolated chloroplasts and a crude suspension of small leaf pieces of Spinacia oleracea were osmotically shocked and subsequently heated. Aliquots of the resulting homogenate including the organelle DNA were directly added to basic reaction mixtures to carry out PCR without additional isolation- or purification steps. A 180 by DNA-fragment from the psbA-gene was amplified in both cases. In parallel, plasmid-DNA (pHT1) bearing the psbA-gene was subjected to PCR retaining unchanged reaction conditions. Identical DNA-fragments were obtained, as the following sequencing revealed. With the meth…

Reaction conditionsSpinaciabiologyPhysiologyPlant Sciencebiology.organism_classificationMolecular biologylaw.inventionChloroplastchemistry.chemical_compoundchemistryChloroplast DNAlawOrganelleChenopodiaceaeAgronomy and Crop ScienceDNAPolymerase chain reactionJournal of Plant Physiology
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Chlorophyll-protein-complexes of thylakoids of wild type and chlorophyll b mutants of Arabidopsis thaliana

1983

Pigment-protein-complexes of two chlorophyll b deficient mutants of Arabidopsis and from the wild type were separated electrophoretically. Light-harvesting proteins were absent in the chlorophyll b free mutant ch(1) and their amount was reduced in the mutant ch(2) which has a reduced content of chlorophyll b. The ratio of CPa:CP I increased with decreasing chlorophyll b content which indicated that the stoichiometry of photosystem II to photosystem I is not constant.

Chlorophyll bPhotosystem IIMutantWild typeCell BiologyPlant ScienceGeneral MedicineBiologyPhotosystem IBiochemistrychemistry.chemical_compoundBiochemistrychemistryChlorophyllThylakoidBotanyPhotosystemPhotosynthesis Research
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