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chtog cdna  (Addgene inc)


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    Addgene inc chtog cdna
    Figure 1. CLASP1 promotes the depolymerization of GMPCPP-stabilized microtubules in a GTP-dependent manner. (A) Schematic of the microtu- bule depolymerization assay. (B) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM <t>chTOG,</t> or 200 nM CLASP1. (C) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1 in the presence of 1 mM GTP. (D) Quantification of microtubule depolymerization rates for the conditions in B and C. N = 50–108 microtubules for each condition across at least two experimental days. Individual data points from different experiments are plotted in different shades, and the means for each experimental repeat are plotted as larger points in the same color. The squares indicate the average of the experimental means, and the vertical bars are the standard errors of the means. See also Video 1. For comparison between the no GTP conditions, a one-way ANOVA followed by Tu- key’s HSD test for multiple comparisons found that the mean rate of microtubule depolymerization was significantly different between the buffer control vs. chTOG (P < 0.001) and chTOG vs. CLASP1 (P < 0.001) in the absence of GTP. There was no statistically significant difference between the buffer control and CLASP1 condition (P = 0.06) in the absence of GTP. Welch’s two-tailed unequal variances t tests were performed for pairwise comparison of the no-GTP vs. GTP conditions and the corresponding P values are indicated on the graph.
    Chtog Cdna, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "CLASPs stabilize the pre-catastrophe intermediate state between microtubule growth and shrinkage."

    Article Title: CLASPs stabilize the pre-catastrophe intermediate state between microtubule growth and shrinkage.

    Journal: The Journal of cell biology

    doi: 10.1083/jcb.202107027

    Figure 1. CLASP1 promotes the depolymerization of GMPCPP-stabilized microtubules in a GTP-dependent manner. (A) Schematic of the microtu- bule depolymerization assay. (B) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1. (C) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1 in the presence of 1 mM GTP. (D) Quantification of microtubule depolymerization rates for the conditions in B and C. N = 50–108 microtubules for each condition across at least two experimental days. Individual data points from different experiments are plotted in different shades, and the means for each experimental repeat are plotted as larger points in the same color. The squares indicate the average of the experimental means, and the vertical bars are the standard errors of the means. See also Video 1. For comparison between the no GTP conditions, a one-way ANOVA followed by Tu- key’s HSD test for multiple comparisons found that the mean rate of microtubule depolymerization was significantly different between the buffer control vs. chTOG (P < 0.001) and chTOG vs. CLASP1 (P < 0.001) in the absence of GTP. There was no statistically significant difference between the buffer control and CLASP1 condition (P = 0.06) in the absence of GTP. Welch’s two-tailed unequal variances t tests were performed for pairwise comparison of the no-GTP vs. GTP conditions and the corresponding P values are indicated on the graph.
    Figure Legend Snippet: Figure 1. CLASP1 promotes the depolymerization of GMPCPP-stabilized microtubules in a GTP-dependent manner. (A) Schematic of the microtu- bule depolymerization assay. (B) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1. (C) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1 in the presence of 1 mM GTP. (D) Quantification of microtubule depolymerization rates for the conditions in B and C. N = 50–108 microtubules for each condition across at least two experimental days. Individual data points from different experiments are plotted in different shades, and the means for each experimental repeat are plotted as larger points in the same color. The squares indicate the average of the experimental means, and the vertical bars are the standard errors of the means. See also Video 1. For comparison between the no GTP conditions, a one-way ANOVA followed by Tu- key’s HSD test for multiple comparisons found that the mean rate of microtubule depolymerization was significantly different between the buffer control vs. chTOG (P < 0.001) and chTOG vs. CLASP1 (P < 0.001) in the absence of GTP. There was no statistically significant difference between the buffer control and CLASP1 condition (P = 0.06) in the absence of GTP. Welch’s two-tailed unequal variances t tests were performed for pairwise comparison of the no-GTP vs. GTP conditions and the corresponding P values are indicated on the graph.

    Techniques Used: Incubation, Comparison, Control, Two Tailed Test



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    Figure 1. CLASP1 promotes the depolymerization of GMPCPP-stabilized microtubules in a GTP-dependent manner. (A) Schematic of the microtu- bule depolymerization assay. (B) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM <t>chTOG,</t> or 200 nM CLASP1. (C) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1 in the presence of 1 mM GTP. (D) Quantification of microtubule depolymerization rates for the conditions in B and C. N = 50–108 microtubules for each condition across at least two experimental days. Individual data points from different experiments are plotted in different shades, and the means for each experimental repeat are plotted as larger points in the same color. The squares indicate the average of the experimental means, and the vertical bars are the standard errors of the means. See also Video 1. For comparison between the no GTP conditions, a one-way ANOVA followed by Tu- key’s HSD test for multiple comparisons found that the mean rate of microtubule depolymerization was significantly different between the buffer control vs. chTOG (P < 0.001) and chTOG vs. CLASP1 (P < 0.001) in the absence of GTP. There was no statistically significant difference between the buffer control and CLASP1 condition (P = 0.06) in the absence of GTP. Welch’s two-tailed unequal variances t tests were performed for pairwise comparison of the no-GTP vs. GTP conditions and the corresponding P values are indicated on the graph.
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    Figure 1. CLASP1 promotes the depolymerization of GMPCPP-stabilized microtubules in a GTP-dependent manner. (A) Schematic of the microtu- bule depolymerization assay. (B) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1. (C) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1 in the presence of 1 mM GTP. (D) Quantification of microtubule depolymerization rates for the conditions in B and C. N = 50–108 microtubules for each condition across at least two experimental days. Individual data points from different experiments are plotted in different shades, and the means for each experimental repeat are plotted as larger points in the same color. The squares indicate the average of the experimental means, and the vertical bars are the standard errors of the means. See also Video 1. For comparison between the no GTP conditions, a one-way ANOVA followed by Tu- key’s HSD test for multiple comparisons found that the mean rate of microtubule depolymerization was significantly different between the buffer control vs. chTOG (P < 0.001) and chTOG vs. CLASP1 (P < 0.001) in the absence of GTP. There was no statistically significant difference between the buffer control and CLASP1 condition (P = 0.06) in the absence of GTP. Welch’s two-tailed unequal variances t tests were performed for pairwise comparison of the no-GTP vs. GTP conditions and the corresponding P values are indicated on the graph.

    Journal: The Journal of cell biology

    Article Title: CLASPs stabilize the pre-catastrophe intermediate state between microtubule growth and shrinkage.

    doi: 10.1083/jcb.202107027

    Figure Lengend Snippet: Figure 1. CLASP1 promotes the depolymerization of GMPCPP-stabilized microtubules in a GTP-dependent manner. (A) Schematic of the microtu- bule depolymerization assay. (B) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1. (C) Representative kymographs of GMPCPP-stabilized microtubules incubated with storage buffer, 200 nM chTOG, or 200 nM CLASP1 in the presence of 1 mM GTP. (D) Quantification of microtubule depolymerization rates for the conditions in B and C. N = 50–108 microtubules for each condition across at least two experimental days. Individual data points from different experiments are plotted in different shades, and the means for each experimental repeat are plotted as larger points in the same color. The squares indicate the average of the experimental means, and the vertical bars are the standard errors of the means. See also Video 1. For comparison between the no GTP conditions, a one-way ANOVA followed by Tu- key’s HSD test for multiple comparisons found that the mean rate of microtubule depolymerization was significantly different between the buffer control vs. chTOG (P < 0.001) and chTOG vs. CLASP1 (P < 0.001) in the absence of GTP. There was no statistically significant difference between the buffer control and CLASP1 condition (P = 0.06) in the absence of GTP. Welch’s two-tailed unequal variances t tests were performed for pairwise comparison of the no-GTP vs. GTP conditions and the corresponding P values are indicated on the graph.

    Article Snippet: The plasmid containing chTOG cDNA was a gift from Stephen Royle (plasmid #69108; Addgene; http://n2t.net/addgene:69108; RRID: Addgene_69108).

    Techniques: Incubation, Comparison, Control, Two Tailed Test