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rabbit myosin7a antibody  (Proteintech)


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    Structured Review

    Proteintech rabbit myosin7a antibody
    Rabbit Myosin7a Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit myosin7a antibody/product/Proteintech
    Average 94 stars, based on 19 article reviews
    rabbit myosin7a antibody - by Bioz Stars, 2026-03
    94/100 stars

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    Proteus Biosciences rabbit myosin7a antibody
    ASO-29 enhances inner and outer hair cell survival. ( A ) Representative whole mount <t>Myosin7a</t> (Myo7a) confocal microscopic projections showing enhanced hair cell survival at 1.0, 2.0 and 3.0 mm from the tip of the cochlear apex (8–24 kHz inclusive) in ASO-29-treated mutants at P30. Distance from the apical tip was translated to frequencies using the cochlear place frequency map shown in . Scale bar: 20 μm. ( B ) Quantification of IHCs and OHCs ± SEM 0.5 to 4 mm from the tip of the cochlear apex (8–32 kHz inclusive). Untreated mutants were compared to the two ASO-29 treatment groups by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: * P < 0.05, ** P < 0.01, n = 5 per group. The number of outer hair cells in ASO-29 mutants and ASO-29 heterozygotes was significantly different only at 4 mm by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: † P < 0.05, n = 5 per group.
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    Average 90 stars, based on 1 article reviews
    rabbit myosin7a antibody - by Bioz Stars, 2026-03
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    Proteus Biosciences myosin7a rabbit antibody
    ASO-29 enhances inner and outer hair cell survival. ( A ) Representative whole mount <t>Myosin7a</t> (Myo7a) confocal microscopic projections showing enhanced hair cell survival at 1.0, 2.0 and 3.0 mm from the tip of the cochlear apex (8–24 kHz inclusive) in ASO-29-treated mutants at P30. Distance from the apical tip was translated to frequencies using the cochlear place frequency map shown in . Scale bar: 20 μm. ( B ) Quantification of IHCs and OHCs ± SEM 0.5 to 4 mm from the tip of the cochlear apex (8–32 kHz inclusive). Untreated mutants were compared to the two ASO-29 treatment groups by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: * P < 0.05, ** P < 0.01, n = 5 per group. The number of outer hair cells in ASO-29 mutants and ASO-29 heterozygotes was significantly different only at 4 mm by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: † P < 0.05, n = 5 per group.
    Myosin7a Rabbit Antibody, supplied by Proteus Biosciences, 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/result/myosin7a rabbit antibody/product/Proteus Biosciences
    Average 90 stars, based on 1 article reviews
    myosin7a rabbit antibody - by Bioz Stars, 2026-03
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    Proteus Biosciences rabbit anti-myosin7a monoclonal antibody (1:1000, proteus bioscience)
    Establishment and validation of the drug-induced hearing loss model. a ABR thresholds of the experimental group increased after drug injection. ***p < 0.001. b Immunofluorescence staining demonstrated HCs loss in the experimental group. <t>Myosin7a</t> (green) was used as a HC marker. Scale bar = 20 μm
    Rabbit Anti Myosin7a Monoclonal Antibody (1:1000, Proteus Bioscience), supplied by Proteus Biosciences, 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/result/rabbit anti-myosin7a monoclonal antibody (1:1000, proteus bioscience)/product/Proteus Biosciences
    Average 90 stars, based on 1 article reviews
    rabbit anti-myosin7a monoclonal antibody (1:1000, proteus bioscience) - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    Image Search Results


    ASO-29 enhances inner and outer hair cell survival. ( A ) Representative whole mount Myosin7a (Myo7a) confocal microscopic projections showing enhanced hair cell survival at 1.0, 2.0 and 3.0 mm from the tip of the cochlear apex (8–24 kHz inclusive) in ASO-29-treated mutants at P30. Distance from the apical tip was translated to frequencies using the cochlear place frequency map shown in . Scale bar: 20 μm. ( B ) Quantification of IHCs and OHCs ± SEM 0.5 to 4 mm from the tip of the cochlear apex (8–32 kHz inclusive). Untreated mutants were compared to the two ASO-29 treatment groups by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: * P < 0.05, ** P < 0.01, n = 5 per group. The number of outer hair cells in ASO-29 mutants and ASO-29 heterozygotes was significantly different only at 4 mm by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: † P < 0.05, n = 5 per group.

    Journal: Nucleic Acids Research

    Article Title: Fetal antisense oligonucleotide therapy for congenital deafness and vestibular dysfunction

    doi: 10.1093/nar/gkaa194

    Figure Lengend Snippet: ASO-29 enhances inner and outer hair cell survival. ( A ) Representative whole mount Myosin7a (Myo7a) confocal microscopic projections showing enhanced hair cell survival at 1.0, 2.0 and 3.0 mm from the tip of the cochlear apex (8–24 kHz inclusive) in ASO-29-treated mutants at P30. Distance from the apical tip was translated to frequencies using the cochlear place frequency map shown in . Scale bar: 20 μm. ( B ) Quantification of IHCs and OHCs ± SEM 0.5 to 4 mm from the tip of the cochlear apex (8–32 kHz inclusive). Untreated mutants were compared to the two ASO-29 treatment groups by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: * P < 0.05, ** P < 0.01, n = 5 per group. The number of outer hair cells in ASO-29 mutants and ASO-29 heterozygotes was significantly different only at 4 mm by two-way repeated measures ANOVA with Tukey's Multiple Comparison Test: † P < 0.05, n = 5 per group.

    Article Snippet: A 1:100 dilution of rabbit Myosin7a (Proteus Biosciences Inc., Ramona, CA, USA) was applied in blocking solution overnight at 4°C with gentle agitation.

    Techniques: Comparison

    Establishment and validation of the drug-induced hearing loss model. a ABR thresholds of the experimental group increased after drug injection. ***p < 0.001. b Immunofluorescence staining demonstrated HCs loss in the experimental group. Myosin7a (green) was used as a HC marker. Scale bar = 20 μm

    Journal: Cell Stress & Chaperones

    Article Title: Upregulation of HSP60 expression in the postnatal rat cochlea and rats with drug-induced hearing loss

    doi: 10.1007/s12192-018-0938-6

    Figure Lengend Snippet: Establishment and validation of the drug-induced hearing loss model. a ABR thresholds of the experimental group increased after drug injection. ***p < 0.001. b Immunofluorescence staining demonstrated HCs loss in the experimental group. Myosin7a (green) was used as a HC marker. Scale bar = 20 μm

    Article Snippet: The samples were then incubated with the following primary antibodies overnight at 4 °C: mouse anti-HSP60 monoclonal antibody (1:100, Millipore), rabbit anti-myosin7a monoclonal antibody (1:1000, Proteus Bioscience), and goat anti-SOX2 polyclonal antibody (1:100, Santa Cruz Biotechnology).

    Techniques: Injection, Immunofluorescence, Staining, Marker

    Upregulation of HSP60 expression in the cochlea after drug injury. a Immunofluorescence staining showed that HSP60 (green) expression was increased in the experimental group. Myosin7a (red) was used as a HC marker. Scale bar = 20 μm. b, c, and d qRT-PCR and Western blot analysis confirmed that the expression levels of Hsp60 gene and HSP60 protein in the experimental group were significantly higher than those in the control group ***p < 0.001

    Journal: Cell Stress & Chaperones

    Article Title: Upregulation of HSP60 expression in the postnatal rat cochlea and rats with drug-induced hearing loss

    doi: 10.1007/s12192-018-0938-6

    Figure Lengend Snippet: Upregulation of HSP60 expression in the cochlea after drug injury. a Immunofluorescence staining showed that HSP60 (green) expression was increased in the experimental group. Myosin7a (red) was used as a HC marker. Scale bar = 20 μm. b, c, and d qRT-PCR and Western blot analysis confirmed that the expression levels of Hsp60 gene and HSP60 protein in the experimental group were significantly higher than those in the control group ***p < 0.001

    Article Snippet: The samples were then incubated with the following primary antibodies overnight at 4 °C: mouse anti-HSP60 monoclonal antibody (1:100, Millipore), rabbit anti-myosin7a monoclonal antibody (1:1000, Proteus Bioscience), and goat anti-SOX2 polyclonal antibody (1:100, Santa Cruz Biotechnology).

    Techniques: Expressing, Immunofluorescence, Staining, Marker, Quantitative RT-PCR, Western Blot