fluorescence confocal microscopy Search Results


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Evident Corporation laser confocal scanning fluorescence microscopy
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confocal microscope  (Evident Corporation)
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Evident Corporation confocal microscope
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ti2 e confocal laser fluorescence microscopy  (Nikon)
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confocal fluorescence microscopy  (Medizinische Hochschule Hannover)
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Medizinische Hochschule Hannover confocal fluorescence microscopy
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
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fibered confocal fluorescence microscopy  (Mauna Kea Technologies)
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Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
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Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
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epi-fluorescence confocal microscopy  (Molecular Dynamics Inc)
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Molecular Dynamics Inc epi-fluorescence confocal microscopy
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
Epi Fluorescence Confocal Microscopy, supplied by Molecular Dynamics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescence or confocal microscopy zeiss lsm pascal  (Carl Zeiss)
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Carl Zeiss fluorescence or confocal microscopy zeiss lsm pascal
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
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intravital fiberoptic confocal fluorescence microscopy cellvizioh system  (Mauna Kea Technologies)
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Mauna Kea Technologies intravital fiberoptic confocal fluorescence microscopy cellvizioh system
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
Intravital Fiberoptic Confocal Fluorescence Microscopy Cellvizioh System, supplied by Mauna Kea Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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thioflavin t (tht) confocal fluorescence microscopy gel  (ibidi GmbH)
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ibidi GmbH thioflavin t (tht) confocal fluorescence microscopy gel
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
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fluorescence confocal microscopy zeiss axio imager with a yokogawa spinning-disc confocal scanner  (Carl Zeiss)
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Carl Zeiss fluorescence confocal microscopy zeiss axio imager with a yokogawa spinning-disc confocal scanner
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
Fluorescence Confocal Microscopy Zeiss Axio Imager With A Yokogawa Spinning Disc Confocal Scanner, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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confocal laser scanning microscopy zeiss lsm pascalexciter fluorescence system  (Carl Zeiss)
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Carl Zeiss confocal laser scanning microscopy zeiss lsm pascalexciter fluorescence system
Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser <t>fluorescence</t> <t>microscopy.</t> BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .
Confocal Laser Scanning Microscopy Zeiss Lsm Pascalexciter Fluorescence System, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser fluorescence microscopy. BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .

Journal: European Journal of Biochemistry

Article Title: Analysis of the thyrotropin‐releasing hormone‐degrading ectoenzyme by site‐directed mutagenesis of cysteine residues

doi: 10.1046/j.1432-1327.2000.01277.x

Figure Lengend Snippet: Subcellular distribution of the truncated GFP‐fusion proteins with either cysteine or serine at position 68, as analyzed by confocal laser fluorescence microscopy. BHK cells were transfected either with the empty pEGFP‐N1 vector (A), the EGFP‐tagged, truncated wild‐type cDNA of TRH‐DE (B) or the corresponding C68S mutant (C) and processed as described in .

Article Snippet: We thank André Wolfstein and Beate Sodeik (Institut für physiologische Chemie, Medizinische Hochschule, Hannover) for experienced support with confocal fluorescence microscopy, Lutz Schomburg for advice and helpful discussions, Uwe Grunenberg for excellent technical assistance, Valerie Ashe for linguistic help and the Deutsche Forschungsgemeinschaft for financial support.

Techniques: Fluorescence, Microscopy, Transfection, Plasmid Preparation, Mutagenesis