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single exponential equation grafit 5  (ERITHACUS SOFTWARE LIMITED)

 
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    ERITHACUS SOFTWARE LIMITED single exponential equation grafit 5
    Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 50 nM fluorescently labeled double-stranded siRNA (aslam-FAM/slam) were rapidly mixed with 500 nM hTRBP (A) or hPACT (B). Data were fitted to a double <t>exponential</t> equation yielding the following rates: k 1 : 11.1 (± 2.3) s -1 and k 2 : 0.02 (± 0.001) s -1 for hTRBP and k 1 : 37.8 (± 2.5) s -1 and k 2 : 0.04 (± 0.005) s -1 for hPACT.
    Single Exponential Equation Grafit 5, supplied by ERITHACUS SOFTWARE LIMITED, 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/single+exponential+equation+grafit+5/pmc04718636-245-6-10?v=ERITHACUS+SOFTWARE+LIMITED
    Average 90 stars, based on 1 article reviews
    single exponential equation grafit 5 - by Bioz Stars, 2026-08
    90/100 stars

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    1) Product Images from "Recombinant hTRBP and hPACT Modulate hAgo2-Catalyzed siRNA-Mediated Target RNA Cleavage In Vitro"

    Article Title: Recombinant hTRBP and hPACT Modulate hAgo2-Catalyzed siRNA-Mediated Target RNA Cleavage In Vitro

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0146814

    Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 50 nM fluorescently labeled double-stranded siRNA (aslam-FAM/slam) were rapidly mixed with 500 nM hTRBP (A) or hPACT (B). Data were fitted to a double exponential equation yielding the following rates: k 1 : 11.1 (± 2.3) s -1 and k 2 : 0.02 (± 0.001) s -1 for hTRBP and k 1 : 37.8 (± 2.5) s -1 and k 2 : 0.04 (± 0.005) s -1 for hPACT.
    Figure Legend Snippet: Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 50 nM fluorescently labeled double-stranded siRNA (aslam-FAM/slam) were rapidly mixed with 500 nM hTRBP (A) or hPACT (B). Data were fitted to a double exponential equation yielding the following rates: k 1 : 11.1 (± 2.3) s -1 and k 2 : 0.02 (± 0.001) s -1 for hTRBP and k 1 : 37.8 (± 2.5) s -1 and k 2 : 0.04 (± 0.005) s -1 for hPACT.

    Techniques Used: Labeling

    The different substrate combinations (ss-siRNA & long target, ds-siRNA & long target, ds-siRNA or ss-siRNA & short target) are depicted as little cartoons on top of the corresponding graph. For target RNA cleavage either 2.5 nM radioactively labeled ICAM-1-IVT (A, B) or s2b (D) were mixed with binary complexes consisting of either 100 nM as2b (A, D) or as2b/s2b (B) and 3 μM hAgo2 in the absence (open circles) or presence of 3 μM hTRBP (closed circles), hTRBP-D12 (open squares) and hPACT (closed squares), respectively. For ds-siRNA cleavage, i.e. passenger cleavage (C), 30 nM 5’-32P-passenger labeled siRNA (as2b/s2b) was mixed with 3 μM hAgo2 in the presence or absence of dsRBPs as described above. Samples were taken at different time points, analyzed by denaturing PAGE (8% for ICAM-1-IVT and 20% for s2b) and detected by autoradiography (Figure H in ). Data shown are averaged from at least three independent measurements. Error bars represent standard deviation. Experimental data were fitted to an exponential equation. Rate constants and corresponding amplitudes are listed in .
    Figure Legend Snippet: The different substrate combinations (ss-siRNA & long target, ds-siRNA & long target, ds-siRNA or ss-siRNA & short target) are depicted as little cartoons on top of the corresponding graph. For target RNA cleavage either 2.5 nM radioactively labeled ICAM-1-IVT (A, B) or s2b (D) were mixed with binary complexes consisting of either 100 nM as2b (A, D) or as2b/s2b (B) and 3 μM hAgo2 in the absence (open circles) or presence of 3 μM hTRBP (closed circles), hTRBP-D12 (open squares) and hPACT (closed squares), respectively. For ds-siRNA cleavage, i.e. passenger cleavage (C), 30 nM 5’-32P-passenger labeled siRNA (as2b/s2b) was mixed with 3 μM hAgo2 in the presence or absence of dsRBPs as described above. Samples were taken at different time points, analyzed by denaturing PAGE (8% for ICAM-1-IVT and 20% for s2b) and detected by autoradiography (Figure H in ). Data shown are averaged from at least three independent measurements. Error bars represent standard deviation. Experimental data were fitted to an exponential equation. Rate constants and corresponding amplitudes are listed in .

    Techniques Used: Labeling, Autoradiography, Standard Deviation

    Representative stopped-flow graphs are shown. Ternary complexes composed of 500 nM hAgo2, 20 nM guide RNA (as2b-FAM) and 40 nM target RNA (s2b) were preassembled and subsequently rapidly mixed with 2 μM unlabeled guide RNA and 500 nM hTRBP-D12 (A) or hTRBP (B). In both cases data could be best fitted using a triple exponential equation, yielding the following rate constants: (A) k -1 : 18.4 (± 1.2) s -1 , k -2 : 0.1 (± 0.007) s -1 , k -3 : 0.002 (± 0.0005) s -1 and (B) k -1 : 15.9 (± 4.6) s -1 , k -2 : 0.05 (± 0.001) s -1 , k -3 : 0.0005 (± 0.0002) s -1 . Rate constants are summarized in .
    Figure Legend Snippet: Representative stopped-flow graphs are shown. Ternary complexes composed of 500 nM hAgo2, 20 nM guide RNA (as2b-FAM) and 40 nM target RNA (s2b) were preassembled and subsequently rapidly mixed with 2 μM unlabeled guide RNA and 500 nM hTRBP-D12 (A) or hTRBP (B). In both cases data could be best fitted using a triple exponential equation, yielding the following rate constants: (A) k -1 : 18.4 (± 1.2) s -1 , k -2 : 0.1 (± 0.007) s -1 , k -3 : 0.002 (± 0.0005) s -1 and (B) k -1 : 15.9 (± 4.6) s -1 , k -2 : 0.05 (± 0.001) s -1 , k -3 : 0.0005 (± 0.0002) s -1 . Rate constants are summarized in .

    Techniques Used:

    Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 20 nM of fluorescently labeled double-stranded siRNA (as2b-FAM/s2B) were pre-incubated with 600 nM hTRBP (A, C) or hPACT (B, D). The binary complexes were subsequently rapidly mixed with either hAgo2 (400 nM in case of A and 600 nM in case of B) or 600 nM hAgo2-PAZ9 (C, D). Data were fitted to an exponential equation. For hAgo2 & hTRBP: k 1 : 28.8 (± 10.8) s -1 , k 2 : 0.33 (±0.03) s -1 and k 3 : 0.002 (± 0.0001) s -1 and for hAgo2 & hPACT: k 1 : 18.6 (± 3.5) s -1 , k 2 : 0.13 (± 0.02) s -1 and k 3 : 0.01 (± 0.001) s -1 were determined. With the mutant hAgo2-PAZ9 the following rate constant were calculated: k 1 : 14.9 (± 2.7) s -1 , k 2 : 0.07 (±0.01) s -1 and k 3 : 0.01 (± 0.0009) s -1 in the presence of hTRBP and k 1 : 16.2 (± 0.6) s -1 , k 2 : 0.38 (±0.01) s -1 and k 3 : 0.007 (± 0.002) s -1 in the presence of hPACT.
    Figure Legend Snippet: Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 20 nM of fluorescently labeled double-stranded siRNA (as2b-FAM/s2B) were pre-incubated with 600 nM hTRBP (A, C) or hPACT (B, D). The binary complexes were subsequently rapidly mixed with either hAgo2 (400 nM in case of A and 600 nM in case of B) or 600 nM hAgo2-PAZ9 (C, D). Data were fitted to an exponential equation. For hAgo2 & hTRBP: k 1 : 28.8 (± 10.8) s -1 , k 2 : 0.33 (±0.03) s -1 and k 3 : 0.002 (± 0.0001) s -1 and for hAgo2 & hPACT: k 1 : 18.6 (± 3.5) s -1 , k 2 : 0.13 (± 0.02) s -1 and k 3 : 0.01 (± 0.001) s -1 were determined. With the mutant hAgo2-PAZ9 the following rate constant were calculated: k 1 : 14.9 (± 2.7) s -1 , k 2 : 0.07 (±0.01) s -1 and k 3 : 0.01 (± 0.0009) s -1 in the presence of hTRBP and k 1 : 16.2 (± 0.6) s -1 , k 2 : 0.38 (±0.01) s -1 and k 3 : 0.007 (± 0.002) s -1 in the presence of hPACT.

    Techniques Used: Labeling, Incubation, Mutagenesis



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    single exponential equation grafit 5  (ERITHACUS SOFTWARE LIMITED)
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    ERITHACUS SOFTWARE LIMITED single exponential equation grafit 5
    Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 50 nM fluorescently labeled double-stranded siRNA (aslam-FAM/slam) were rapidly mixed with 500 nM hTRBP (A) or hPACT (B). Data were fitted to a double <t>exponential</t> equation yielding the following rates: k 1 : 11.1 (± 2.3) s -1 and k 2 : 0.02 (± 0.001) s -1 for hTRBP and k 1 : 37.8 (± 2.5) s -1 and k 2 : 0.04 (± 0.005) s -1 for hPACT.
    Single Exponential Equation Grafit 5, supplied by ERITHACUS SOFTWARE LIMITED, 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/single+exponential+equation+grafit+5/pmc04718636-245-6-10?v=ERITHACUS+SOFTWARE+LIMITED
    Average 90 stars, based on 1 article reviews
    single exponential equation grafit 5 - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

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    Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 50 nM fluorescently labeled double-stranded siRNA (aslam-FAM/slam) were rapidly mixed with 500 nM hTRBP (A) or hPACT (B). Data were fitted to a double exponential equation yielding the following rates: k 1 : 11.1 (± 2.3) s -1 and k 2 : 0.02 (± 0.001) s -1 for hTRBP and k 1 : 37.8 (± 2.5) s -1 and k 2 : 0.04 (± 0.005) s -1 for hPACT.

    Journal: PLoS ONE

    Article Title: Recombinant hTRBP and hPACT Modulate hAgo2-Catalyzed siRNA-Mediated Target RNA Cleavage In Vitro

    doi: 10.1371/journal.pone.0146814

    Figure Lengend Snippet: Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 50 nM fluorescently labeled double-stranded siRNA (aslam-FAM/slam) were rapidly mixed with 500 nM hTRBP (A) or hPACT (B). Data were fitted to a double exponential equation yielding the following rates: k 1 : 11.1 (± 2.3) s -1 and k 2 : 0.02 (± 0.001) s -1 for hTRBP and k 1 : 37.8 (± 2.5) s -1 and k 2 : 0.04 (± 0.005) s -1 for hPACT.

    Article Snippet: Data were fitted using a single exponential equation (Grafit 5, Erithacus Software).

    Techniques: Labeling

    The different substrate combinations (ss-siRNA & long target, ds-siRNA & long target, ds-siRNA or ss-siRNA & short target) are depicted as little cartoons on top of the corresponding graph. For target RNA cleavage either 2.5 nM radioactively labeled ICAM-1-IVT (A, B) or s2b (D) were mixed with binary complexes consisting of either 100 nM as2b (A, D) or as2b/s2b (B) and 3 μM hAgo2 in the absence (open circles) or presence of 3 μM hTRBP (closed circles), hTRBP-D12 (open squares) and hPACT (closed squares), respectively. For ds-siRNA cleavage, i.e. passenger cleavage (C), 30 nM 5’-32P-passenger labeled siRNA (as2b/s2b) was mixed with 3 μM hAgo2 in the presence or absence of dsRBPs as described above. Samples were taken at different time points, analyzed by denaturing PAGE (8% for ICAM-1-IVT and 20% for s2b) and detected by autoradiography (Figure H in ). Data shown are averaged from at least three independent measurements. Error bars represent standard deviation. Experimental data were fitted to an exponential equation. Rate constants and corresponding amplitudes are listed in .

    Journal: PLoS ONE

    Article Title: Recombinant hTRBP and hPACT Modulate hAgo2-Catalyzed siRNA-Mediated Target RNA Cleavage In Vitro

    doi: 10.1371/journal.pone.0146814

    Figure Lengend Snippet: The different substrate combinations (ss-siRNA & long target, ds-siRNA & long target, ds-siRNA or ss-siRNA & short target) are depicted as little cartoons on top of the corresponding graph. For target RNA cleavage either 2.5 nM radioactively labeled ICAM-1-IVT (A, B) or s2b (D) were mixed with binary complexes consisting of either 100 nM as2b (A, D) or as2b/s2b (B) and 3 μM hAgo2 in the absence (open circles) or presence of 3 μM hTRBP (closed circles), hTRBP-D12 (open squares) and hPACT (closed squares), respectively. For ds-siRNA cleavage, i.e. passenger cleavage (C), 30 nM 5’-32P-passenger labeled siRNA (as2b/s2b) was mixed with 3 μM hAgo2 in the presence or absence of dsRBPs as described above. Samples were taken at different time points, analyzed by denaturing PAGE (8% for ICAM-1-IVT and 20% for s2b) and detected by autoradiography (Figure H in ). Data shown are averaged from at least three independent measurements. Error bars represent standard deviation. Experimental data were fitted to an exponential equation. Rate constants and corresponding amplitudes are listed in .

    Article Snippet: Data were fitted using a single exponential equation (Grafit 5, Erithacus Software).

    Techniques: Labeling, Autoradiography, Standard Deviation

    Representative stopped-flow graphs are shown. Ternary complexes composed of 500 nM hAgo2, 20 nM guide RNA (as2b-FAM) and 40 nM target RNA (s2b) were preassembled and subsequently rapidly mixed with 2 μM unlabeled guide RNA and 500 nM hTRBP-D12 (A) or hTRBP (B). In both cases data could be best fitted using a triple exponential equation, yielding the following rate constants: (A) k -1 : 18.4 (± 1.2) s -1 , k -2 : 0.1 (± 0.007) s -1 , k -3 : 0.002 (± 0.0005) s -1 and (B) k -1 : 15.9 (± 4.6) s -1 , k -2 : 0.05 (± 0.001) s -1 , k -3 : 0.0005 (± 0.0002) s -1 . Rate constants are summarized in .

    Journal: PLoS ONE

    Article Title: Recombinant hTRBP and hPACT Modulate hAgo2-Catalyzed siRNA-Mediated Target RNA Cleavage In Vitro

    doi: 10.1371/journal.pone.0146814

    Figure Lengend Snippet: Representative stopped-flow graphs are shown. Ternary complexes composed of 500 nM hAgo2, 20 nM guide RNA (as2b-FAM) and 40 nM target RNA (s2b) were preassembled and subsequently rapidly mixed with 2 μM unlabeled guide RNA and 500 nM hTRBP-D12 (A) or hTRBP (B). In both cases data could be best fitted using a triple exponential equation, yielding the following rate constants: (A) k -1 : 18.4 (± 1.2) s -1 , k -2 : 0.1 (± 0.007) s -1 , k -3 : 0.002 (± 0.0005) s -1 and (B) k -1 : 15.9 (± 4.6) s -1 , k -2 : 0.05 (± 0.001) s -1 , k -3 : 0.0005 (± 0.0002) s -1 . Rate constants are summarized in .

    Article Snippet: Data were fitted using a single exponential equation (Grafit 5, Erithacus Software).

    Techniques:

    Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 20 nM of fluorescently labeled double-stranded siRNA (as2b-FAM/s2B) were pre-incubated with 600 nM hTRBP (A, C) or hPACT (B, D). The binary complexes were subsequently rapidly mixed with either hAgo2 (400 nM in case of A and 600 nM in case of B) or 600 nM hAgo2-PAZ9 (C, D). Data were fitted to an exponential equation. For hAgo2 & hTRBP: k 1 : 28.8 (± 10.8) s -1 , k 2 : 0.33 (±0.03) s -1 and k 3 : 0.002 (± 0.0001) s -1 and for hAgo2 & hPACT: k 1 : 18.6 (± 3.5) s -1 , k 2 : 0.13 (± 0.02) s -1 and k 3 : 0.01 (± 0.001) s -1 were determined. With the mutant hAgo2-PAZ9 the following rate constant were calculated: k 1 : 14.9 (± 2.7) s -1 , k 2 : 0.07 (±0.01) s -1 and k 3 : 0.01 (± 0.0009) s -1 in the presence of hTRBP and k 1 : 16.2 (± 0.6) s -1 , k 2 : 0.38 (±0.01) s -1 and k 3 : 0.007 (± 0.002) s -1 in the presence of hPACT.

    Journal: PLoS ONE

    Article Title: Recombinant hTRBP and hPACT Modulate hAgo2-Catalyzed siRNA-Mediated Target RNA Cleavage In Vitro

    doi: 10.1371/journal.pone.0146814

    Figure Lengend Snippet: Representative stopped-flow graphs are shown. The inserts show the reaction on a shorter time scale. 20 nM of fluorescently labeled double-stranded siRNA (as2b-FAM/s2B) were pre-incubated with 600 nM hTRBP (A, C) or hPACT (B, D). The binary complexes were subsequently rapidly mixed with either hAgo2 (400 nM in case of A and 600 nM in case of B) or 600 nM hAgo2-PAZ9 (C, D). Data were fitted to an exponential equation. For hAgo2 & hTRBP: k 1 : 28.8 (± 10.8) s -1 , k 2 : 0.33 (±0.03) s -1 and k 3 : 0.002 (± 0.0001) s -1 and for hAgo2 & hPACT: k 1 : 18.6 (± 3.5) s -1 , k 2 : 0.13 (± 0.02) s -1 and k 3 : 0.01 (± 0.001) s -1 were determined. With the mutant hAgo2-PAZ9 the following rate constant were calculated: k 1 : 14.9 (± 2.7) s -1 , k 2 : 0.07 (±0.01) s -1 and k 3 : 0.01 (± 0.0009) s -1 in the presence of hTRBP and k 1 : 16.2 (± 0.6) s -1 , k 2 : 0.38 (±0.01) s -1 and k 3 : 0.007 (± 0.002) s -1 in the presence of hPACT.

    Article Snippet: Data were fitted using a single exponential equation (Grafit 5, Erithacus Software).

    Techniques: Labeling, Incubation, Mutagenesis