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Sutter Instrument Company
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Sutter Instrument Company
lambda ls with smart shutter ![]() Lambda Ls With Smart Shutter, supplied by Sutter Instrument Company, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/lambda+ls+with+smart+shutter/lambda+ls+with+smart+shutter/pmc04727948-69-34-40 Average 90 stars, based on 1 article reviews
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Sutter Instrument Company
lambda ls illumination and a lambda 10-b smart shutter ![]() Lambda Ls Illumination And A Lambda 10 B Smart Shutter, supplied by Sutter Instrument Company, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/lambda+ls+with+smart+shutter/lambda+ls+illumination+and+a+lambda+10+b+smart+shutter/pmc02924298-203-5-9 Average 90 stars, based on 1 article reviews
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Journal: The Journal of General Physiology
Article Title: Transition metal ion FRET to measure short-range distances at the intracellular surface of the plasma membrane
doi: 10.1085/jgp.201511530
Figure Lengend Snippet: Cell unroofing is useful for a variety of adherent cell types. (A) Cartoon of unroofing approach in which cells are stained with R18 (red) after sonication. (B) Unroofed and stained ND7/23, PC-12, F-11, and HEK293T/17 cells imaged with epifluorescence microscopy. Scale bar applies to all images and is 50 µm.
Article Snippet: To label, patches were perfused with 100–250 nM R18 in recording solution (130 mM NaCl, 3 mM HEPES, and 0.2 mM EDTA, pH 7.2) for 1–2 min. To monitor labeling, patches were excited with
Techniques: Staining, Sonication, Epifluorescence Microscopy
Journal: The Journal of General Physiology
Article Title: Transition metal ion FRET to measure short-range distances at the intracellular surface of the plasma membrane
doi: 10.1085/jgp.201511530
Figure Lengend Snippet: tmFRET between R18 and Co 2+ -C18-NTA in inside-out patches from a Xenopus oocyte. (A) Bright-field and epifluorescence images from a representative patch. Fluorescence images from patches with either 0 or 1 µM Co 2+ before (left) or after (middle) application of C18-NTA and after 20 mM EDTA (right). Scale bar in top left image applies to all images and is 20 µm. (B) Patch fluorescence in Co 2+ was normalized to patch fluorescence in EDTA before and after C18-NTA ( n = 4). Mean (lines) and individual (points) patch values are shown. Asterisk indicates significance at P < 0.05.
Article Snippet: To label, patches were perfused with 100–250 nM R18 in recording solution (130 mM NaCl, 3 mM HEPES, and 0.2 mM EDTA, pH 7.2) for 1–2 min. To monitor labeling, patches were excited with
Techniques: Fluorescence