540nm Bandpass Filter

540nm light, a green wavelength in the visible spectrum, offers high transmission in its narrow bandwidth and minimal interference from adjacent wavelengths.

  • Application 1: In fluorescence microscopy, it isolates emission signals from green fluorescent proteins (GFPs) to enhance imaging clarity in biological samples.
  • Application 2: In environmental spectroscopy, it enables precise measurement of chlorophyll absorption in water bodies for aquatic health monitoring.
  • Application 3: In industrial color sorting, it filters light to identify materials with specific green spectral responses during automated quality control.

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540nm Bandpass Filter
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US5968738A - Two-reporter FACS analysis of mammalian cells using green fluorescent proteins

US5968738A - Two-reporter FACS analysis of mammalian cells using green fluorescent proteins

Context: A Flow Cytometry (FACS) system designed to analyze mammalian cells expressing two different reporter genes simultaneously.

Usage of Filter: The filter is used in the optical detection path to define a specific measurement window, specifically measuring a "first signal" at a wavelength lambda em between 500 nm and 540 nm.

Function: It isolates the green fluorescence emission (typically from GFP or its variants) while blocking excitation light and crosstalk from other fluorophores (like red-emitting reporters).

Result: This achieves the simultaneous, quantitative detection of two distinct transcriptional elements within a single cell, enabling complex gene expression analysis.

US8730601B2 - Fluorescence observation system and set of filters

US8730601B2 - Fluorescence observation system and set of filters

Context: A fluorescence microscope or observation system designed to visualize fluorescent samples with high contrast.

Usage of Filter: The filter is utilized as a threshold wavelength selector, specifically operating within a range from 510 nm to 540 nm (often as a short-pass or bandpass edge) to separate fluorescence from the excitation light.

Function: It acts to discriminate between the excitation light (which is reflected or scattered) and the desired fluorescence signal, ensuring only the "signal" light reaches the observer or camera.

Result: This achieves a high S/N (Signal-to-Noise) ratio, allowing for clear observation of faint fluorescent structures against a dark background.

US5377676A - Method for determining the biodistribution of substances using fluorescence spectroscopy

US5377676A - Method for determining the biodistribution of substances using fluorescence spectroscopy

Context: A medical diagnostic system (often using a fiber-optic probe) to track how a fluorescent substance distributes within biological tissue.

Usage of Filter: The filter is used as a wavelength selection device to isolate the fluorescence emission centered around or including 540 nm (a common emission region for tracers like fluorescein or eosin).

Function: It filters the light returning from the tissue to ensure the detector only measures the intensity of the fluorescent tracer, rejecting reflected tissue light or autofluorescence outside this band.

Result: This achieves the real-time, in vivo determination of drug or substance biodistribution, helping to verify if a therapeutic agent has reached its target tissue.

US20140340680A1 - Apparatus and method for measurement of an analyte

US20140340680A1 - Apparatus and method for measurement of an analyte

Context: An optical detection unit, potentially for a mobile or point-of-care device, used to measure the concentration of a specific analyte (e.g., hemoglobin or a chemical marker).

Usage of Filter: A specific 540 nm bandpass filter with a 10 nm bandwidth is placed in front of the optical sensor.

Function: It restricts the light entering the sensor to a very narrow spectral band (535–545 nm), which corresponds to the peak absorption or emission of the target analyte.

Result: This achieves precise quantification of the analyte by eliminating spectral interference from ambient light or other sample components.

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