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sequence encoding ecfp frb  (Addgene inc)


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    Addgene inc sequence encoding ecfp frb
    Sequence Encoding Ecfp Frb, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ecfp+w66a/pmc12307597-276-15-28?v=Addgene+inc
    Average 93 stars, based on 7 article reviews
    sequence encoding ecfp frb - by Bioz Stars, 2026-07
    93/100 stars

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    Addgene inc giantin
    Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag <t>and</t> <t>FIREmate–</t> <t>eCFP–Giantin</t> (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed
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    Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and <t>FIREmate–</t> <t>eCFP–Giantin</t> (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed
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    Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and <t>FIREmate–</t> <t>eCFP–Giantin</t> (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed
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    Addgene inc firemate ecfp sequence
    Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and <t>FIREmate–</t> <t>eCFP–Giantin</t> (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed
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    Image Search Results


    Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and FIREmate– eCFP–Giantin (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed

    Journal: Nature methods

    Article Title: A fluorogenic chemically induced dimerization technology for controlling, imaging and sensing protein proximity.

    doi: 10.1038/s41592-023-01988-8

    Figure Lengend Snippet: Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and FIREmate– eCFP–Giantin (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed

    Article Snippet: The plasmid pAG1171 for the expression of FIREmate–eCFP– Giantin was constructed by replacing the sequence coding for FRB– eCFP(W66A)–Giantin by FIREmate–eCFP sequence in the Addgene vector (#67903) coding for FRB–eCFP(W66A)–Giantin16.

    Techniques: Control, Confocal Microscopy

    Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and FIREmate– eCFP–Giantin (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed

    Journal: Nature methods

    Article Title: A fluorogenic chemically induced dimerization technology for controlling, imaging and sensing protein proximity.

    doi: 10.1038/s41592-023-01988-8

    Figure Lengend Snippet: Fig. 2 | CATCHFIRE enables the control of protein dimerization with high temporal control. a–f, HeLa cells coexpressing mCherry–FIREtag and FIREmate– eCFP–Giantin (a,b), FIREmate–eCFP–Cb5 (c,d), Lyn11–FIREmate–eCFP (e,f) were treated with 10 μM match550 and imaged by timelapse confocal microscopy. Representative confocal micrographs of cells before (0 min) and after (5 min) addition of match550 (Supplementary Videos 9–11) (a,c,e). Experiments were repeated three times with similar results. Temporal evolution of the CATCHFIRE signal (b,d,f). Data represent the mean ± s.d. of three independent experiments (n = 11 cells (b), 15 cells (d) and 15 cells (f)). g,h, HeLa cells coexpressing mCherry–FIREtag and Giantin–IRFP–FIREmate were treated with 10 μM match550 for 240 s, washed for 212 s and then treated with 10 μM match540 for 212 s and washed

    Article Snippet: The plasmid pAG1211 for the expression of FRB–eCFP–Giantin was constructed by replacing the sequence coding for eCFP(W66A) by the eCFP sequence in the Addgene vector (#67903) coding for FRB–eCFP(W66A)–Giantin16.

    Techniques: Control, Confocal Microscopy