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microtubule depolymerization  (Cytoskeleton Inc)


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    Structured Review

    Cytoskeleton Inc microtubule depolymerization
    Microtubule Depolymerization, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 96/100, based on 97 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/microtubule+depolymerization/Tubulin+polymerization+assay/pm40593938-122-6-19
    Average 96 stars, based on 97 article reviews
    microtubule depolymerization - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Migration:

    Article Title: Update on 13 Syndromes Affecting Craniofacial and Dental Structures
    Article Snippet: Opitz GBBB syndrome , Xp22.2 , MID1 , GO:0005622 intracellular GO:0005737 cytoplasm GO:0005819 spindle GO:0005829 cytosol GO:0005856 cytoskeleton , GO:0005515 protein binding GO:0008017 microtubule binding GO:0008270 zinc ion binding GO:0016740 transferase activity GO:0031625 ubiquitin protein ligase binding , GO:0000226 microtubule cytoskeleton organization GO:0007026 negative regulation of microtubule depolymerization GO:0032874 post regulation of stress-activated MAPK cascade GO:0035372 protein localization to microtubule. .. , 22q11.23 , SPECC1L , GO:0005815 microtubule organizing center GO:0005819 spindle GO:0005829 cytosol GO:0005856 cytoskeleton GO:0005921 gap junction , / , GO:0007026 negative regulation of microtubule depolymerization GO:0007049 cell cycle GO:0007155 cell adhesion GO:0016477 cell migration GO:0030036 actin cytoskeleton organization. .. Smith-Lemli-Opitz syndrome , 11q13.4 , DHCR7 , GO:0005640 nuclear outer membrane GO:0005783 endoplasmic reticulum GO:0005789 endoplasmic reticulum membrane GO:0005829 cytosol , GO:0009918 sterol delta7 reductase activity GO:0016491 oxidoreductase activity GO:0016628 oxidoreductase activity, acting on the CH-CH group of donors, NAD, or NADP as acceptor GO:0047598 7-dehydrocholesterol reductase activity GO:0050661 NADP binding , GO:0001568 blood vessel development GO:0006629 lipid metabolic process GO:0006694 steroid biosynthetic process GO:0006695 cholesterol biosynthetic process GO:0008202 steroid metabolic process.

    Sedimentation:

    Article Title: OsKinesin-13A Is an Active Microtubule Depolymerase Involved in Glume Length Regulation via Affecting Cell Elongation
    Article Snippet: Cells with well-resolved individual microtubules (most of them were at the late elongation or differentiation stage) were used to analyze microtubule dynamics with the Image J software ( http://imagej.nih.gov/ij/ ) according to the described method . .. Sedimentation analysis of microtubule depolymerization was performed by mixing the purified GST (as a control), the OsKinesin-13A-motor protein, or the full-length OsKinesin-13A protein with 1 μM taxol-stabilized microtubules (Cytoskeleton Inc.) in a PEM-KOH buffer (80 mM PIPES, 1 mM EGTA, 1 mM MgCl 2 , 10 μM taxol, 30 mM KCl, pH 6.9) plus 2 mM ATP or AMPPNP. ..

    Purification:

    Article Title: OsKinesin-13A Is an Active Microtubule Depolymerase Involved in Glume Length Regulation via Affecting Cell Elongation
    Article Snippet: Cells with well-resolved individual microtubules (most of them were at the late elongation or differentiation stage) were used to analyze microtubule dynamics with the Image J software ( http://imagej.nih.gov/ij/ ) according to the described method . .. Sedimentation analysis of microtubule depolymerization was performed by mixing the purified GST (as a control), the OsKinesin-13A-motor protein, or the full-length OsKinesin-13A protein with 1 μM taxol-stabilized microtubules (Cytoskeleton Inc.) in a PEM-KOH buffer (80 mM PIPES, 1 mM EGTA, 1 mM MgCl 2 , 10 μM taxol, 30 mM KCl, pH 6.9) plus 2 mM ATP or AMPPNP. ..

    Control:

    Article Title: OsKinesin-13A Is an Active Microtubule Depolymerase Involved in Glume Length Regulation via Affecting Cell Elongation
    Article Snippet: Cells with well-resolved individual microtubules (most of them were at the late elongation or differentiation stage) were used to analyze microtubule dynamics with the Image J software ( http://imagej.nih.gov/ij/ ) according to the described method . .. Sedimentation analysis of microtubule depolymerization was performed by mixing the purified GST (as a control), the OsKinesin-13A-motor protein, or the full-length OsKinesin-13A protein with 1 μM taxol-stabilized microtubules (Cytoskeleton Inc.) in a PEM-KOH buffer (80 mM PIPES, 1 mM EGTA, 1 mM MgCl 2 , 10 μM taxol, 30 mM KCl, pH 6.9) plus 2 mM ATP or AMPPNP. ..

    Dispersion:

    Article Title: High-intensity light disrupts intracellular organelle dynamics via microtubule depolymerization.
    Article Snippet: .. HIWL-induced xanthosomes dispersion was mediated by microtubule depolymerization The movement of pigment granules within chromatophores is facilitated by the cytoskeleton, primarily composed of microfilaments and microtubules37. ..

    Inhibition:

    Article Title: Body handedness is directed by genetically determined cytoskeletal dynamics in the early embryo.
    Article Snippet: .. The fact that SD, which determines the direction of cell cleavage, occurs inde-ticular strain of L. stagnalis or a particular species of Lymnaea. pendent of spindle and astral microtubules is an interesting observation for the understanding of the molecu-To investigate the interdependence of spindle orientation and blastomere shape in the dextral and sinistral lar basis of cell polarity and cell axis determination prior to cytokinesis in general.embryos, we examined the effect of inhibition of spindle assembly by using the microtubule depolymerization The involvement of the actin cytoskeleton in the spindle orientation and blastomere shape was investigatedagent nocodazole. ..



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    Figure 3. Effects of ferric derisomaltose and darbepoetin alfa on cell viability in erythroid F36E cells. F36E cells were treated with 10 nM of <t>PTX</t> plus various concentrations of ferric derisomaltose and/or darbepoetin alfa for 48 h. (A) F36E cells were treated with various concentrations of PTX. (B) F36E cells were treated with 10 nM of PTX plus various concentrations of ferric derisomaltose or darbepoetin alfa. (C) F36E cells were treated with 10 nM of PTX, 10 nM of PTX plus 10 nM of darbepoetin alfa and 10 nM of PTX plus 10 nM of darbepoetin alfa plus various concentrations of ferric derisomaltose. PTX, <t>paclitaxel.</t>
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    Figure 3. Effects of ferric derisomaltose and darbepoetin alfa on cell viability in erythroid F36E cells. F36E cells were treated with 10 nM of PTX plus various concentrations of ferric derisomaltose and/or darbepoetin alfa for 48 h. (A) F36E cells were treated with various concentrations of PTX. (B) F36E cells were treated with 10 nM of PTX plus various concentrations of ferric derisomaltose or darbepoetin alfa. (C) F36E cells were treated with 10 nM of PTX, 10 nM of PTX plus 10 nM of darbepoetin alfa and 10 nM of PTX plus 10 nM of darbepoetin alfa plus various concentrations of ferric derisomaltose. PTX, paclitaxel.

    Journal: International journal of molecular sciences

    Article Title: Effects of Darbepoetin Alfa and Ferric Derisomaltose Plus Darbepoetin Alfa in Functional Iron-Deficiency Anemia.

    doi: 10.3390/ijms26052203

    Figure Lengend Snippet: Figure 3. Effects of ferric derisomaltose and darbepoetin alfa on cell viability in erythroid F36E cells. F36E cells were treated with 10 nM of PTX plus various concentrations of ferric derisomaltose and/or darbepoetin alfa for 48 h. (A) F36E cells were treated with various concentrations of PTX. (B) F36E cells were treated with 10 nM of PTX plus various concentrations of ferric derisomaltose or darbepoetin alfa. (C) F36E cells were treated with 10 nM of PTX, 10 nM of PTX plus 10 nM of darbepoetin alfa and 10 nM of PTX plus 10 nM of darbepoetin alfa plus various concentrations of ferric derisomaltose. PTX, paclitaxel.

    Article Snippet: The third-generation high-dose intravenous iron supplement ferric derisomaltose (Monofer; Pharmbio Korea, Seoul, Republic of Korea), the ESA darbepoetin alfa (CKD11101, Nesbell; Chong Kun Dang Pharm, Seoul, Republic of Korea) [22], and the microtubule depolymerization inhibitor paclitaxel (PTX) (Selleck Chemicals, Houston, TX, USA) were obtained from the sources shown.

    Techniques:

    Figure 4. Effects of ferric derisomaltose, darbepoetin alfa, and PTX on cell viability in GC cell lines. SNU620 and SNU638 GC cells were treated with 10 nM PTX plus various concentrations of ferric derisomaltose or darbepoetin alfa for 48 h. PTX, paclitaxel.

    Journal: International journal of molecular sciences

    Article Title: Effects of Darbepoetin Alfa and Ferric Derisomaltose Plus Darbepoetin Alfa in Functional Iron-Deficiency Anemia.

    doi: 10.3390/ijms26052203

    Figure Lengend Snippet: Figure 4. Effects of ferric derisomaltose, darbepoetin alfa, and PTX on cell viability in GC cell lines. SNU620 and SNU638 GC cells were treated with 10 nM PTX plus various concentrations of ferric derisomaltose or darbepoetin alfa for 48 h. PTX, paclitaxel.

    Article Snippet: The third-generation high-dose intravenous iron supplement ferric derisomaltose (Monofer; Pharmbio Korea, Seoul, Republic of Korea), the ESA darbepoetin alfa (CKD11101, Nesbell; Chong Kun Dang Pharm, Seoul, Republic of Korea) [22], and the microtubule depolymerization inhibitor paclitaxel (PTX) (Selleck Chemicals, Houston, TX, USA) were obtained from the sources shown.

    Techniques: