Methods in molecular biology (Clifton, N.J.), ISSN 1064-3745, 2008, Volume 418, p. 13
The avidin-biotin bond is the strongest known biological interaction between a ligand and a protein (Kd = 1.3 x 10-15 M at pH 5.0) (1). The affinity is so high...
Biotin - chemistry | Antibodies - chemistry | Binding Sites, Antibody
Biotin - chemistry | Antibodies - chemistry | Binding Sites, Antibody
Journal Article
Methods in molecular biology (Clifton, N.J.), ISSN 1064-3745, 2008, Volume 418, p. 1
The high-affinity avidin-biotin system has found applications in different fields of biotechnology, including immunoassays, histochemistry, affinity...
Enzymes - chemistry | Antibodies - chemistry | Avidin - chemistry | Chromatography, Affinity - methods | Succinimides - chemistry
Enzymes - chemistry | Antibodies - chemistry | Avidin - chemistry | Chromatography, Affinity - methods | Succinimides - chemistry
Journal Article
Methods in molecular biology (Clifton, N.J.), ISSN 1064-3745, 2005, Volume 295, pp. 135 - 154
Antibodies can be conjugated to biotin by a number of chemical means. They can then be used in immunochemical procedures in conjunction with secondary reagents...
Biotin - chemistry | Avidin - chemistry | Animals | Immunochemistry | Immunoglobulin Fab Fragments - chemistry
Biotin - chemistry | Avidin - chemistry | Animals | Immunochemistry | Immunoglobulin Fab Fragments - chemistry
Journal Article
Journal of Histochemistry and Cytochemistry, ISSN 0022-1554, 12/2003, Volume 51, Issue 12, pp. 1699 - 1712
Amine-reactive N-hydroxysuccinimidyl esters of Alexa Fluor fluorescent dyes with principal absorption maxima at about 555 nm, 633 nm, 647 nm, 660 nm, 680 nm,...
Flow cytometry | Cy dyes | Microscopy | Fluorescent Bioconjugates | Photostability | Alexa Fluor dyes | FRET | Immunofluorescence | Long-wavelength dyes | fluorescent bioconjugates | FLUOROCHROMES | LABELING REAGENTS | photostability | PROBES | CELL BIOLOGY | ANTIGEN-DETECTION | flow cytometry | microscopy | long-wavelength dyes | FLOW-CYTOMETRY | SUCCINIMIDYL ESTERS | PROTEINS | AVIDIN | BINDING | immunofluorescence | BRIGHT | Immunohistochemistry | Water | Succinates - chemistry | Carbocyanines - chemistry | Humans | Benzopyrans - chemistry | Flow Cytometry | Cattle | Brain - ultrastructure | Epithelial Cells - cytology | Photobleaching | Fluorescent Dyes - chemistry | Cells, Cultured | Solubility | Epithelial Cells - ultrastructure | Rats | Mitochondrial Proton-Translocating ATPases - metabolism | Pulmonary Artery - enzymology | Pulmonary Artery - cytology | Pulmonary Artery - ultrastructure | Animals | T-Lymphocytes - cytology | Proteins - chemistry | Spectrophotometry | Indoles - chemistry | Microscopy, Fluorescence
Flow cytometry | Cy dyes | Microscopy | Fluorescent Bioconjugates | Photostability | Alexa Fluor dyes | FRET | Immunofluorescence | Long-wavelength dyes | fluorescent bioconjugates | FLUOROCHROMES | LABELING REAGENTS | photostability | PROBES | CELL BIOLOGY | ANTIGEN-DETECTION | flow cytometry | microscopy | long-wavelength dyes | FLOW-CYTOMETRY | SUCCINIMIDYL ESTERS | PROTEINS | AVIDIN | BINDING | immunofluorescence | BRIGHT | Immunohistochemistry | Water | Succinates - chemistry | Carbocyanines - chemistry | Humans | Benzopyrans - chemistry | Flow Cytometry | Cattle | Brain - ultrastructure | Epithelial Cells - cytology | Photobleaching | Fluorescent Dyes - chemistry | Cells, Cultured | Solubility | Epithelial Cells - ultrastructure | Rats | Mitochondrial Proton-Translocating ATPases - metabolism | Pulmonary Artery - enzymology | Pulmonary Artery - cytology | Pulmonary Artery - ultrastructure | Animals | T-Lymphocytes - cytology | Proteins - chemistry | Spectrophotometry | Indoles - chemistry | Microscopy, Fluorescence
Journal Article
Journal of Histochemistry and Cytochemistry, ISSN 0022-1554, 09/1999, Volume 47, Issue 9, pp. 1179 - 1188
Alexa 350, Alexa 430, Alexa 488, Alexa 532, Alexa 546, Alexa 568, and Alexa 594 dyes are a new series of fluorescent dyes with emission/excitation spectra...
Flow cytometry | Dyes | Fluorescent conjugates | Microscopy | Immunofluorescence | Photostability | ANTIBODIES | IMMUNOFLUORESCENCE MICROSCOPY | dyes | photostability | FLUOROPHORE | CELL BIOLOGY | LISSAMINE RHODAMINE | flow cytometry | microscopy | TEXAS RED | fluorescent conjugates | DERIVATIVES | immunofluorescence | Xanthenes | Propidium | Animals | Fluorescein-5-isothiocyanate | Microscopy, Fluorescence - methods | Photochemistry - methods | Humans | Cells, Cultured | Streptavidin | Fluorescent Dyes
Flow cytometry | Dyes | Fluorescent conjugates | Microscopy | Immunofluorescence | Photostability | ANTIBODIES | IMMUNOFLUORESCENCE MICROSCOPY | dyes | photostability | FLUOROPHORE | CELL BIOLOGY | LISSAMINE RHODAMINE | flow cytometry | microscopy | TEXAS RED | fluorescent conjugates | DERIVATIVES | immunofluorescence | Xanthenes | Propidium | Animals | Fluorescein-5-isothiocyanate | Microscopy, Fluorescence - methods | Photochemistry - methods | Humans | Cells, Cultured | Streptavidin | Fluorescent Dyes
Journal Article
Analytical Biochemistry, ISSN 0003-2697, 2002, Volume 308, Issue 2, pp. 343 - 357
The high-affinity binding of biotin to avidin, streptavidin, and related proteins has been exploited for decades. However, a disadvantage of the...
Succinimidyl ester | Bioconjugates | Amine-reactive | Affinity chromatography | Desthiobiotin | Streptavidin | Reversible binding | Biotin | Avidin | BIOTINYLATION | affinity chromatography | CHEMISTRY, ANALYTICAL | streptavidin | avidin | RECOGNITION | reversible binding | ANALOGS | desthiobiotin | BIOCHEMISTRY & MOLECULAR BIOLOGY | biotin | BIOCHEMICAL RESEARCH METHODS | SELECTIVE RETRIEVAL | SUBUNITS | MULTILAYERS | amine-reactive | bioconjugates | LIGANDS | succinimidyl ester | AFFINITY COLUMNS | TECHNOLOGY | RESIDUES | Recombinant Proteins - metabolism | Rabbits | Humans | Avidin - metabolism | Tubulin - metabolism | Animals | Carrier Proteins - metabolism | Streptavidin - metabolism | Immunoglobulin G - immunology | Sepharose - chemistry | Protein Binding | Biotin - metabolism | Indicators and Reagents | Ligands | Chromatography, Affinity - methods | Biotin - analogs & derivatives | Immunoglobulin G - metabolism
Succinimidyl ester | Bioconjugates | Amine-reactive | Affinity chromatography | Desthiobiotin | Streptavidin | Reversible binding | Biotin | Avidin | BIOTINYLATION | affinity chromatography | CHEMISTRY, ANALYTICAL | streptavidin | avidin | RECOGNITION | reversible binding | ANALOGS | desthiobiotin | BIOCHEMISTRY & MOLECULAR BIOLOGY | biotin | BIOCHEMICAL RESEARCH METHODS | SELECTIVE RETRIEVAL | SUBUNITS | MULTILAYERS | amine-reactive | bioconjugates | LIGANDS | succinimidyl ester | AFFINITY COLUMNS | TECHNOLOGY | RESIDUES | Recombinant Proteins - metabolism | Rabbits | Humans | Avidin - metabolism | Tubulin - metabolism | Animals | Carrier Proteins - metabolism | Streptavidin - metabolism | Immunoglobulin G - immunology | Sepharose - chemistry | Protein Binding | Biotin - metabolism | Indicators and Reagents | Ligands | Chromatography, Affinity - methods | Biotin - analogs & derivatives | Immunoglobulin G - metabolism
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 12/1999, Volume 274, Issue 53, pp. 37611 - 37619
Vitronectin (VN) is a high affinity heparin-binding protein. The physiological role of this binding has hitherto received little attention, and its molecular...
SELF-ASSOCIATION | ADHESION | COAGULASE-NEGATIVE STAPHYLOCOCCI | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | ANTITHROMBIN | AUREUS | HEPARAN-SULFATE PROTEOGLYCANS | MULTIMERIC VITRONECTIN | IDENTIFICATION | S-PROTEIN VITRONECTIN | Endothelium, Vascular - cytology | Heparin - metabolism | Endothelium, Vascular - metabolism | Humans | Cells, Cultured | Vitronectin - chemistry | Protein Binding | Spectrometry, Fluorescence | Protein Conformation | Kinetics | Vitronectin - metabolism
SELF-ASSOCIATION | ADHESION | COAGULASE-NEGATIVE STAPHYLOCOCCI | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | ANTITHROMBIN | AUREUS | HEPARAN-SULFATE PROTEOGLYCANS | MULTIMERIC VITRONECTIN | IDENTIFICATION | S-PROTEIN VITRONECTIN | Endothelium, Vascular - cytology | Heparin - metabolism | Endothelium, Vascular - metabolism | Humans | Cells, Cultured | Vitronectin - chemistry | Protein Binding | Spectrometry, Fluorescence | Protein Conformation | Kinetics | Vitronectin - metabolism
Journal Article
ELECTROPHORESIS, ISSN 0173-0835, 04/2001, Volume 22, Issue 5, pp. 896 - 905
A two‐color fluorescence detection method is described based upon covalently coupling the succinimidyl ester of BODIPY FL‐X to proteins immobilized on...
Fluorescence | Electroblot | Protein stain | Dichromatic | Immunodetection | BLOTS | CHEMISTRY, ANALYTICAL | protein stain | BIOCHEMICAL RESEARCH METHODS | electroblot | 2-DIMENSIONAL GEL-ELECTROPHORESIS | WHEAT-GERM-AGGLUTININ | CONCANAVALIN-A | COLLOIDAL GOLD | immunodetection | EGG-WHITE | fluorescence | dichromatic | PROTEOMICS | OVALBUMIN | Acridines - chemistry | Boron Compounds - chemistry | Phosphates | Blotting, Western - methods | Egg Proteins - analysis | Rats | Spectrometry, Fluorescence | Proteins - analysis | Alkaline Phosphatase | Tubulin - analysis | Animals | Carboxylic Acids | Cattle | Polyvinyls | Indicators and Reagents | Brain Chemistry | Electrophoresis - methods | Glycoproteins - analysis | Fluorescent Dyes | Fibroblasts - chemistry
Fluorescence | Electroblot | Protein stain | Dichromatic | Immunodetection | BLOTS | CHEMISTRY, ANALYTICAL | protein stain | BIOCHEMICAL RESEARCH METHODS | electroblot | 2-DIMENSIONAL GEL-ELECTROPHORESIS | WHEAT-GERM-AGGLUTININ | CONCANAVALIN-A | COLLOIDAL GOLD | immunodetection | EGG-WHITE | fluorescence | dichromatic | PROTEOMICS | OVALBUMIN | Acridines - chemistry | Boron Compounds - chemistry | Phosphates | Blotting, Western - methods | Egg Proteins - analysis | Rats | Spectrometry, Fluorescence | Proteins - analysis | Alkaline Phosphatase | Tubulin - analysis | Animals | Carboxylic Acids | Cattle | Polyvinyls | Indicators and Reagents | Brain Chemistry | Electrophoresis - methods | Glycoproteins - analysis | Fluorescent Dyes | Fibroblasts - chemistry
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 12/2007, Volume 418, pp. 1 - 12
Conference Proceeding
Methods in Molecular Biology, ISSN 1064-3745, 12/2007, Volume 418, pp. 13 - 23
Conference Proceeding
Analytical Biochemistry, ISSN 0003-2697, 05/1999, Volume 269, Issue 2, pp. 410 - 417
5-(Pentafluorobenzoylamino)fluorescein (PFB-F), a new thiol-reactive molecule was synthesized to improve the detection limits and specificity of the assays for...
CELLS | HOMOCYSTEINE | CHEMISTRY, ANALYTICAL | ASSAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | PERFORMANCE LIQUID-CHROMATOGRAPHY | THIOLS | ELECTROCHEMICAL DETECTION | MONOCHLOROBIMANE | RESISTANCE | NITROGEN MUSTARDS | EXPRESSION | Fluorescent Dyes - chemical synthesis | Chromatography, High Pressure Liquid - methods | Chromatography, Thin Layer - methods | Humans | Recombinant Fusion Proteins - analysis | Substrate Specificity | Fluoresceins - chemical synthesis | Endothelium, Vascular - enzymology | Endothelium, Vascular - chemistry | Glutathione Transferase - analysis | Animals | Cattle | Glutathione - analysis
CELLS | HOMOCYSTEINE | CHEMISTRY, ANALYTICAL | ASSAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | PERFORMANCE LIQUID-CHROMATOGRAPHY | THIOLS | ELECTROCHEMICAL DETECTION | MONOCHLOROBIMANE | RESISTANCE | NITROGEN MUSTARDS | EXPRESSION | Fluorescent Dyes - chemical synthesis | Chromatography, High Pressure Liquid - methods | Chromatography, Thin Layer - methods | Humans | Recombinant Fusion Proteins - analysis | Substrate Specificity | Fluoresceins - chemical synthesis | Endothelium, Vascular - enzymology | Endothelium, Vascular - chemistry | Glutathione Transferase - analysis | Animals | Cattle | Glutathione - analysis
Journal Article
Analytical Biochemistry, ISSN 0003-2697, 09/1997, Volume 251, Issue 2, pp. 144 - 152
We have prepared casein conjugates of two BODIPY dyes for use as fluorogenic protease substrates in homogeneous assays. Both conjugates are labeled to such an...
K CO BIOCHEMICAL RESEARCH METHODS | K EA CHEMISTRY, ANALYTICAL | CHEMISTRY, ANALYTICAL | K CQ BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | ENERGY-TRANSFER | PROTEINS | Hydrolysis | Xanthenes | Animals | Protease Inhibitors - analysis | Caseins - chemistry | Fluorescein-5-isothiocyanate | Fluorescent Antibody Technique, Direct | Humans | Spectrometry, Fluorescence | Endopeptidases - analysis | Boron Compounds | Fluorescent Dyes | Measurement | Biological products | Casein | Protease inhibitors | Proteases | Proteolysis | Analysis | Fluorescein | Fluorescence
K CO BIOCHEMICAL RESEARCH METHODS | K EA CHEMISTRY, ANALYTICAL | CHEMISTRY, ANALYTICAL | K CQ BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | ENERGY-TRANSFER | PROTEINS | Hydrolysis | Xanthenes | Animals | Protease Inhibitors - analysis | Caseins - chemistry | Fluorescein-5-isothiocyanate | Fluorescent Antibody Technique, Direct | Humans | Spectrometry, Fluorescence | Endopeptidases - analysis | Boron Compounds | Fluorescent Dyes | Measurement | Biological products | Casein | Protease inhibitors | Proteases | Proteolysis | Analysis | Fluorescein | Fluorescence
Journal Article
Brain Research, ISSN 0006-8993, 2001, Volume 920, Issue 1, pp. 226 - 238
We have developed and tested the biological activity and specificity of a novel fluorescent dextran-Texas Red-nerve growth factor (DTR-NGF) conjugate. DTR-NGF...
Confocal microscopy | Rat | NGF transport | Antibody receptor blockade | Superior cervical ganglion | RETROGRADE AXONAL-TRANSPORT | rat | TYROSINE KINASE | AFFINITY NEUROTROPHIN RECEPTOR | superior cervical ganglion | CROSS-LINKING | COMPARTMENTED CULTURES | NEUROSCIENCES | antibody receptor blockade | NERVE GROWTH-FACTOR | SIGNAL-TRANSDUCTION | FACTOR BINDING | confocal microscopy | BIOLOGICAL-ACTIVITY | PC12 CELLS | Iris - metabolism | Sympathetic Nervous System - cytology | Antibodies, Blocking | Rats | Axonal Transport - physiology | Male | Nerve Growth Factors - metabolism | Rats, Sprague-Dawley | Sympathetic Nervous System - metabolism | Dose-Response Relationship, Drug | Xanthenes | Microscopy, Confocal | Animals | Dextrans | Image Processing, Computer-Assisted | Receptor, trkA - metabolism | Iris - innervation | Neurons - metabolism | Receptor, Nerve Growth Factor - metabolism | Fluorescent Dyes
Confocal microscopy | Rat | NGF transport | Antibody receptor blockade | Superior cervical ganglion | RETROGRADE AXONAL-TRANSPORT | rat | TYROSINE KINASE | AFFINITY NEUROTROPHIN RECEPTOR | superior cervical ganglion | CROSS-LINKING | COMPARTMENTED CULTURES | NEUROSCIENCES | antibody receptor blockade | NERVE GROWTH-FACTOR | SIGNAL-TRANSDUCTION | FACTOR BINDING | confocal microscopy | BIOLOGICAL-ACTIVITY | PC12 CELLS | Iris - metabolism | Sympathetic Nervous System - cytology | Antibodies, Blocking | Rats | Axonal Transport - physiology | Male | Nerve Growth Factors - metabolism | Rats, Sprague-Dawley | Sympathetic Nervous System - metabolism | Dose-Response Relationship, Drug | Xanthenes | Microscopy, Confocal | Animals | Dextrans | Image Processing, Computer-Assisted | Receptor, trkA - metabolism | Iris - innervation | Neurons - metabolism | Receptor, Nerve Growth Factor - metabolism | Fluorescent Dyes
Journal Article
Analytical Biochemistry, ISSN 0003-2697, 01/1997, Volume 244, Issue 2, pp. 277 - 282
This paper describes the application of 3-(4-carboxybenzoyl)quinoline-2-carboxaldehyde (CBQCA), a sensitive fluorogenic reagent for detection of amines, to the...
K CO BIOCHEMICAL RESEARCH METHODS | K EA CHEMISTRY, ANALYTICAL | CHEMISTRY, ANALYTICAL | MICROGRAM QUANTITIES | K CQ BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | PRIMARY AMINES | FLUORESCAMINE | Quinolines | Benzoates | Molecular Weight | Solutions | Spectrometry, Fluorescence | Sulfhydryl Compounds - chemistry | Lipoproteins - chemistry | Proteins - chemistry | Fluorescent Dyes | Dithiothreitol - pharmacology | Proteins | Quinoline | Alkaloids | Biological products | Blood lipids | Chemical tests and reagents
K CO BIOCHEMICAL RESEARCH METHODS | K EA CHEMISTRY, ANALYTICAL | CHEMISTRY, ANALYTICAL | MICROGRAM QUANTITIES | K CQ BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | PRIMARY AMINES | FLUORESCAMINE | Quinolines | Benzoates | Molecular Weight | Solutions | Spectrometry, Fluorescence | Sulfhydryl Compounds - chemistry | Lipoproteins - chemistry | Proteins - chemistry | Fluorescent Dyes | Dithiothreitol - pharmacology | Proteins | Quinoline | Alkaloids | Biological products | Blood lipids | Chemical tests and reagents
Journal Article
Analytical Biochemistry, ISSN 0003-2697, 12/1996, Volume 243, Issue 1, pp. 41 - 45
This paper describes a spectrophotometric assay that can measure the inorganic pyrophosphate produced from various enzymatic reactions. This is a coupled assay...
BIOCHEMISTRY & MOLECULAR BIOLOGY | ASSAY | Guanosine - analogs & derivatives | Spectrophotometry, Atomic | Luciferases - metabolism | Acetate-CoA Ligase - metabolism | Thionucleosides | Luminescent Measurements | Diphosphates - analysis | Measurement | Phosphates | Biological products | Ligases | Methods
BIOCHEMISTRY & MOLECULAR BIOLOGY | ASSAY | Guanosine - analogs & derivatives | Spectrophotometry, Atomic | Luciferases - metabolism | Acetate-CoA Ligase - metabolism | Thionucleosides | Luminescent Measurements | Diphosphates - analysis | Measurement | Phosphates | Biological products | Ligases | Methods
Journal Article
Bioconjugate Chemistry, ISSN 1043-1802, 07/1996, Volume 7, Issue 4, pp. 482 - 489
Texas Red sulfonyl chloride (TR-SC) and Lissamine rhodamine B sulfonyl chloride (LRB-SC) are popular dyes often used to prepare red fluorescent conjugates that...
CHEMISTRY | FLUOROPHORES | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS
CHEMISTRY | FLUOROPHORES | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS
Journal Article
Journal of Immunological Methods, ISSN 0022-1759, 10/1998, Volume 219, Issue 1-2, pp. 57 - 68
Fluorescent probes serve as sensitive tools for obtaining structural and functional information in cellular systems. In spite of the high sensitivity provided...
Microspheres | CD4 | Phycobiliproteins | CD3 | Beads | Epidermal growth factor receptor | Latex | microspheres | epidermal growth factor receptor | BIOCHEMICAL RESEARCH METHODS | beads | IMMUNOLOGY | EPIDERMAL GROWTH-FACTOR | latex | phycobiliproteins | Flow Cytometry - methods | Jurkat Cells | Humans | Receptors, Cell Surface - analysis | Fluorescent Dyes - metabolism | Spectrometry, Fluorescence | CD3 Complex - analysis | Animals | CD4 Antigens - analysis | Polystyrenes | Fluorescein | Phycoerythrin | Streptavidin | Mice | Tumor Cells, Cultured | 3T3 Cells | ErbB Receptors - analysis
Microspheres | CD4 | Phycobiliproteins | CD3 | Beads | Epidermal growth factor receptor | Latex | microspheres | epidermal growth factor receptor | BIOCHEMICAL RESEARCH METHODS | beads | IMMUNOLOGY | EPIDERMAL GROWTH-FACTOR | latex | phycobiliproteins | Flow Cytometry - methods | Jurkat Cells | Humans | Receptors, Cell Surface - analysis | Fluorescent Dyes - metabolism | Spectrometry, Fluorescence | CD3 Complex - analysis | Animals | CD4 Antigens - analysis | Polystyrenes | Fluorescein | Phycoerythrin | Streptavidin | Mice | Tumor Cells, Cultured | 3T3 Cells | ErbB Receptors - analysis
Journal Article
Analytical Biochemistry, ISSN 0003-2697, 1992, Volume 207, Issue 2, pp. 267 - 279
A series of chemically reactive, fluorescent rhodol derivatives was prepared and evaluated. Reactive functional groups included activated esters, amines,...
LASER-DYES | RED | CHARGE SEPARATION | BLUE | BIOCHEMISTRY & MOLECULAR BIOLOGY | Fluorescent Dyes - chemical synthesis | Xanthenes - chemical synthesis | Fluorescent Dyes - chemistry | Affinity Labels - chemistry | Xanthenes - chemistry | Drug Stability | Spectrometry, Fluorescence | Structure-Activity Relationship | Flow Cytometry | Indicators and Reagents | Molecular Structure | Spectrophotometry | Microscopy, Fluorescence | Affinity Labels - chemical synthesis | Hydrogen-Ion Concentration
LASER-DYES | RED | CHARGE SEPARATION | BLUE | BIOCHEMISTRY & MOLECULAR BIOLOGY | Fluorescent Dyes - chemical synthesis | Xanthenes - chemical synthesis | Fluorescent Dyes - chemistry | Affinity Labels - chemistry | Xanthenes - chemistry | Drug Stability | Spectrometry, Fluorescence | Structure-Activity Relationship | Flow Cytometry | Indicators and Reagents | Molecular Structure | Spectrophotometry | Microscopy, Fluorescence | Affinity Labels - chemical synthesis | Hydrogen-Ion Concentration
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 12/1999, Volume 274, Issue 53, p. 37611
Vitronectin (VN) is a high affinity heparin-binding protein. The physiological role of this binding has hitherto received little attention, and its molecular...
Journal Article
Analytical Biochemistry, ISSN 0003-2697, 05/1999, Volume 269, Issue 2, pp. 410 - 417
Journal Article
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