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anti rock1  (Bioss)


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    Structured Review

    Bioss anti rock1
    Anti Rock1, supplied by Bioss, used in various techniques. Bioz Stars score: 91/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti rock1/product/Bioss
    Average 91 stars, based on 6 article reviews
    anti rock1 - by Bioz Stars, 2026-02
    91/100 stars

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    Bioss anti rock1 antibody bs 1166r
    RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, <t>ROCK1</t> and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm
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    Average 91 stars, based on 1 article reviews
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    Bioss rock1 polyclonal antibody
    RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, <t>ROCK1</t> and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm
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    Bioss antirock1 antibody
    RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, <t>ROCK1</t> and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm
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    Bioss bs-1166r
    RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, <t>ROCK1</t> and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm
    Bs 1166r, supplied by Bioss, 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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    rock1  (Bioss)
    91
    Bioss rock1
    RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, <t>ROCK1</t> and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm
    Rock1, supplied by Bioss, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rock1/product/Bioss
    Average 91 stars, based on 1 article reviews
    rock1 - by Bioz Stars, 2026-02
    91/100 stars
      Buy from Supplier

    Image Search Results


    RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, ROCK1 and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm

    Journal: Cell Proliferation

    Article Title: RAB14 GTPase is essential for actin‐based asymmetric division during mouse oocyte maturation

    doi: 10.1111/cpr.13104

    Figure Lengend Snippet: RAB14 knockdown disrupts cytoplasmic actin assembly in mouse oocytes. (A) Representative images of actin filament distribution at the oocyte cortex and cytoplasm in the control group, RAB14‐KD group and rescue group. Red, F‐actin. Bar = 20 μm. (B) No significant difference was observed between control oocytes, Rab14 siRNA‐injected oocytes and rescue oocytes for the F‐actin fluorescent intensities at the cortex ( P > .1); however, F‐actin fluorescent intensities in the cytoplasm were decreased in the Rab14 siRNA‐injected oocytes compared with the control and rescue oocytes. *, significant difference ( P < .05). (C) Quantitative analysis of the relative intensity of ARP2, N‐WASP, ROCK1 and p‐cofilin in oocytes by Western blot. The results indicated that ROCK1 and p‐cofilin protein expression were significantly reduced in oocytes after RAB14 depletion. **, significant difference ( P < .01); *, significant difference ( P < .05). (D) Representative images of ROCK1 in the control and RAB14‐KD oocytes. ROCK1 fluorescent intensities decreased in the RAB14‐KD oocytes compared with the control oocytes. *, significant difference ( P < .05). Bar = 20 μm

    Article Snippet: A rabbit polyclonal anti‐ROCK1 antibody (bs‐1166R) (for immnuofluorescence staining) was purchased from Bioss.

    Techniques: Injection, Western Blot, Expressing