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Fluorescence Polarization FP

FP (fluorescence polarization) Several Interdependent change in molecular size and rotational diffusion of labeled moiety changes FP signal... [Pg.88]

FIGURE 4.1 Assays commonly used in GPCR research. SPA = scintillation proximity assay FP = fluorescence polarization TR-FRET = time-resolved fluorescence resonance energy transfer FCS = fluorescence correlation spectroscopy SeAP = secreted alkaline phosphate TF = transcription factor EFC = enzyme fragment complementation DMR = dynamic mass redistribution CDS = cellular dielectric spectroscopy. [Pg.61]

FI = fluorescence intensity FP = fluorescent polarization TRF = time-resolved, fluorescence Lum = luminance Abs = absorbance. [Pg.188]

A = agar plate-based assay S = solution-based assay FRET = fluorescence resonance energy transfer FP = fluorescence polarization FCS = fluorescence correlation spectroscopy... [Pg.160]

FP - fluorescence polarization FI - fluorescence intensity CNG2 - cAMP gated ion channel 2 CRE - cAMP response element SRE - serum response element SEAP - secreted alkaline phosphatase. For further details see Refs. [111-113]... [Pg.964]

Fig. 7. Fluorescence polarization (FP). (a) The formation of the large FITC—protein A—IgG complex which leads to a net increase in plane polarized light transmitted from the solution. Molecular weights of the protein A-FITC, IgG, and complex are ca 43,000, 150,000, and 343,000, respectively, (b) Detection of IgG by fluorescence polarization immunoassay using A, a laboratory fluorimeter where (O) represents AP = change in polarization, and B, a portable detection unit where (D) is —fiV = change in voltage (27). The field detector proved to be more sensitive than the fluorimeter. Fig. 7. Fluorescence polarization (FP). (a) The formation of the large FITC—protein A—IgG complex which leads to a net increase in plane polarized light transmitted from the solution. Molecular weights of the protein A-FITC, IgG, and complex are ca 43,000, 150,000, and 343,000, respectively, (b) Detection of IgG by fluorescence polarization immunoassay using A, a laboratory fluorimeter where (O) represents AP = change in polarization, and B, a portable detection unit where (D) is —fiV = change in voltage (27). The field detector proved to be more sensitive than the fluorimeter.
Parameters Radiometric proximity assays (SPA, Flashplate) Fluorescence polarization (FP) Time- resolved fluorescence (HTRF) Amplified luminescence (ALPHAScreen) Enzyme (p-galactosidase) complementation Electrochemilumines cence... [Pg.378]

Product and services of interest include genomics, proteomics, custom research and services, and instruments, accessories, consumables and software. PerkinElmer proprietary technologies include time-resolved fluorescence which is employed in the sensitive Wallac DELFIA system and Wallac LANCE homogeneous assay system, and fluorescence polarization, [FP]2 , a robust fluorescence-based technique for receptor binding assays that is both fast and easy-to-use. [Pg.274]

Fluorescence microscopy, 16 483 Fluorescence polarization (FP), 14 149-150 Fluorescence polarization immunoassay (FPIA), 12 97... [Pg.370]

IMAP (immobilized metal ion affinity-based fluorescence polarization) Molecular Devices Trivalent metal ion containing beads bind to phosphorylated peptide producing FP signal change... [Pg.88]

The availability of anti-phosphotyrosine antibodies, anti-phosphopeptide antibodies, and antibodies to fluorescent ADP analogs enabled the performance of several homogeneous methods using fluorophores including TR-FRET and fluorescence polarization (FP). [Pg.8]

Anisotropy can be measured when a fluorescent molecule is excited with polarized light. The ratio of emission intensity in each polarization plane, parallel and perpendicular relative to the excitation polarization plane, gives a measure of anisotropy, more commonly and incorrectly referred to in HTS as fluorescence polarization (FP). This anisotropy is proportional to the Brownian rotational motion of the fluorophore. [Pg.9]

In addition to biosensor experiments, the interaction YTXs-PDEs was also confirmed by eheek-ing the variations in the fluorescence polarization (FP) of PDEs labeled with eatboxy-fluoreseein. FP units change when the molecule is bound to the toxin. With this technique, a good relationship of toxin concentration to FP units can be observed (Alfonso et al. 2005), whieh again eonfirms PDEs-YTXs binding. [Pg.204]

Because of the very stringent reliability requirements for diagnostic applications, the only homogeneous techniques that have survived in this field are the fluorescence polarization (FP) methods originally developed by AbbotE and the homogeneous time resolved fluorescence (HTRF) and TRACE approaches developed later by CIS bio international. [Pg.234]

Fluorescence Polarization FP Specific antibody recognizes fluorescence labelled peptides or substrates High... [Pg.330]


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See also in sourсe #XX -- [ Pg.361 , Pg.409 ]




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