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mouse anti β integrin myospheroid  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank mouse anti β integrin myospheroid
    Mouse Anti β Integrin Myospheroid, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 96/100, based on 39 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+%CE%B2+integrin+myospheroid/anti-integrin+betaPS/pmc08550105-73-11-15
    Average 96 stars, based on 39 article reviews
    mouse anti β integrin myospheroid - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Labeling:

    Article Title: Characterization of the Drosophila Adult Hematopoietic System Reveals a Rare Cell Population With Differentiation and Proliferation Potential
    Article Snippet: .. The following antibodies were used: mouse anti-P1/NimC1 , mouse anti-Col , mouse anti-β integrin/Myospheroid (CF6.G11, DSHB), mouse anti-Antp (8C11, DSHB), rabbit anti-GFP (Torrey Pines), anti-DIG coupled to alkaline phosphatase (Roche) and Alexa-fluor labeled secondary antibodies (Molecular Probes). .. Nuclei were stained with DAPI and the actin cytoskeleton with fluorescent labeled phalloidin (Molecular Probes).



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    mouse anti myospheroid β integrin  (Developmental Studies Hybridoma Bank)
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    Effects of larval stretching on MJM positioning. (A) Max intensity projections of confocal images of anterior and posterior MTJs for the indicated genotypes stained for <t>β-integrin</t> (gray) and nuclei (green). White asterisks mark trachea branches, which are not part of the muscle. Scale bar is 10 μm (B-F) Tukey boxplots showing the distance between MJMs and the MTJ in larval that have not been stretched (not stretched), larvae dissected immediately after stretching (stretched), larva that have been stretched and dissected after a 2 h recovery (stretched +2 h). (G) Cartoon of MJM position in stretching experiments. Summary of the stretching experiments from (A-F) . For sake of simplicity, only one MJM is represented for each MTJ. Black arrows indicate the direction of the change in nuclear positioning. * p < 0.05, *** p < 0.0005, **** p < 0.0001.
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    Effects of larval stretching on MJM positioning. (A) Max intensity projections of confocal images of anterior and posterior MTJs for the indicated genotypes stained for β-integrin (gray) and nuclei (green). White asterisks mark trachea branches, which are not part of the muscle. Scale bar is 10 μm (B-F) Tukey boxplots showing the distance between MJMs and the MTJ in larval that have not been stretched (not stretched), larvae dissected immediately after stretching (stretched), larva that have been stretched and dissected after a 2 h recovery (stretched +2 h). (G) Cartoon of MJM position in stretching experiments. Summary of the stretching experiments from (A-F) . For sake of simplicity, only one MJM is represented for each MTJ. Black arrows indicate the direction of the change in nuclear positioning. * p < 0.05, *** p < 0.0005, **** p < 0.0001.

    Journal: Frontiers in Physiology

    Article Title: Specialized Positioning of Myonuclei Near Cell-Cell Junctions

    doi: 10.3389/fphys.2018.01531

    Figure Lengend Snippet: Effects of larval stretching on MJM positioning. (A) Max intensity projections of confocal images of anterior and posterior MTJs for the indicated genotypes stained for β-integrin (gray) and nuclei (green). White asterisks mark trachea branches, which are not part of the muscle. Scale bar is 10 μm (B-F) Tukey boxplots showing the distance between MJMs and the MTJ in larval that have not been stretched (not stretched), larvae dissected immediately after stretching (stretched), larva that have been stretched and dissected after a 2 h recovery (stretched +2 h). (G) Cartoon of MJM position in stretching experiments. Summary of the stretching experiments from (A-F) . For sake of simplicity, only one MJM is represented for each MTJ. Black arrows indicate the direction of the change in nuclear positioning. * p < 0.05, *** p < 0.0005, **** p < 0.0001.

    Article Snippet: Antibodies for larva filet staining were used at the following final dilutions: rat anti- tyrosinated tubulin, 1:400 (MAB1864; Millipore), mouse anti-myospheroid (β-integrin), 1:100 (CF.6G11, Developmental Studies Hybridoma Bank).

    Techniques: Staining