{"id":2552,"date":"2015-09-15T03:30:29","date_gmt":"2015-09-15T07:30:29","guid":{"rendered":"http:\/\/localhost:8888\/iridian\/?page_id=2552"},"modified":"2017-12-17T17:31:50","modified_gmt":"2017-12-17T22:31:50","slug":"flow-cytometry","status":"publish","type":"page","link":"https:\/\/iridian.jp\/en\/application-areas\/flow-cytometry\/","title":{"rendered":"Flow Cytometry"},"content":{"rendered":"<p>Flow Cytometry systems rely on sophisticated fluid dynamics along with optical analysis to count and in some cases sort cell populations based on the fluorescence properties of the cells of interest.\u00a0\u00a0 Cells labeled with fluorophores pass individually in a stream of fluid through an excitation beam causing the cells to fluoresce. The fluorescence signal is detected and the population of each fluorophore (and correspond tagged cell) is counted. In some systems the cells can then be sorted into groupings according to their fluorophore labels. The data generated by this technology can be used in diagnosis of health issues, medical research, and other areas of cell study such as micro-biology.<\/p>\n<p>Flow cytometers leverage many of the same filters and principles used in <a href=\"https:\/\/iridian.jp\/en\/application-areas\/fluorescence\/\">fluorescence spectroscopy<\/a>.\u00a0 Excitation filters can be used to ensure that only the desired wavelength is incident upon the sample flow. Emission filters are used in front of the detectors (typically photo-diodes) to clean-up the fluorescence signal, rejecting the excitation\u00a0light and any undesirable light emitted by other fluorophores.\u00a0 A series of long and short pass dichroic filters are used at angles of incidence of 45\u00b0 to direct the emitted signal to the detector corresponding to the colour of the fluorophore.<\/p>\n<p>Iridian\u2019s flow cytometry filters have high transmittance, steep edges, low ripple and deep blocking.\u00a0 We offer custom design and manufacture where required.<\/p>\n<p>Further information on Iridian\u2019s flow cytometry filters:<\/p>\n<p>[nice-button link=&#8221;\/product-category\/spectroscopic\/bandpass\/laser-line\/&#8221;] Excitation (Laser Lines)[\/nice-button]<\/p>\n<p>&nbsp;<\/p>\n<p>[nice-button link=&#8221;\/product-category\/spectroscopic\/bandpass\/emission-cytometry\/&#8221;] Emission[\/nice-button]<\/p>\n<p>&nbsp;<\/p>\n<p>[nice-button link=&#8221;\/product-category\/spectroscopic\/dichroic\/short-pass-cytometry\/&#8221;] Dichroic \u2013 SPF[\/nice-button]<\/p>\n<p>&nbsp;<\/p>\n<p>[nice-button link=&#8221;\/product-category\/spectroscopic\/dichroic\/long-pass-cytometry\/&#8221;] Dichroic \u2013 LPF[\/nice-button]<\/p>\n<p>&nbsp;<\/p>\n<p>For custom flow cytometry filter solutions please <a href=\"https:\/\/iridian.jp\/en\/company-facts\/contact-us\/sales-team\/\">contact us<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Flow Cytometry systems rely on sophisticated fluid dynamics along with optical analysis to count and in some cases sort cell populations based on the fluorescence properties of the cells of interest.\u00a0\u00a0 Cells labeled with fluorophores pass individually in a stream of fluid through an excitation beam causing the cells to fluoresce. The fluorescence signal is [&hellip;]<\/p>\n","protected":false},"author":147,"featured_media":0,"parent":121,"menu_order":184,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-2552","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.7 (Yoast SEO v28.4) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Flow Cytometry - Iridian Spectral Technologies<\/title>\n<meta name=\"description\" content=\"Iridian\u2019s flow cytometry filters have high transmittance, steep edges, low ripple and deep blocking. 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