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rabbit anti mouse rankl polyclonal antibody  (OriGene)


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    Structured Review

    OriGene rabbit anti mouse rankl polyclonal antibody
    Rabbit Anti Mouse Rankl Polyclonal Antibody, supplied by OriGene, 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/product/rabbit+anti+mouse+rankl+polyclonal+antibody/RANKL+(TNFSF11)+Rabbit+Polyclonal+Antibody/pm33247463-46-6-11
    Average 90 stars, based on 1 article reviews
    rabbit anti mouse rankl polyclonal antibody - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: T cell and periosteum cooperation in osteoclastogenesis induced by lipopolysaccharide injection in transplanted mouse tibia
    Article Snippet: Sections were then immersed in rabbit anti-mouse RANKL polyclonal antibody (1:200; Acris Antibodies, Rockville, MD, USA) and CD3 polyclonal antibody (1:200; Abcam, Cambridge, UK) at 4 °C overnight.

    Article Title: High-mobility group box 1 released by traumatic occlusion accelerates bone resorption in the root furcation area in mice.
    Article Snippet: Traumatic occlusion leads to destruction of alveolar bone without the presence of bacterial infection1-3 and is characterized by angular bone resorption in the proximal area and furcation area.4,5 Accumulated evidence has demonstrated that biologically active substances in the bacterial plaque induce a local inflammatory response in the periodontal tissues and that these host responses promote bone resorption through osteoclasts in periodontitis.6,7 In contrast, relatively few studies have examined the molecular mechanisms that trigger bone resorption by traumatic occlusion.8 A clear understanding of the mechanism of bone resorption due to traumatic Received: 5 May 2019 | Revised: 20 September 2020 | Accepted: 30 September 2020 DOI: 10.1111/jre.12813



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    HMW-HA downregulated osteoclastic bone resorption in ovariectomized mice through the downregulation of <t>RANKL-expressing</t> osteocytes. A The area analyzed for osteoclast parameters is indicated in the box in yellow. B Representative images of TRAP staining. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate osteoclasts. Red bars in high-power images indicate scale bars (50 μm). C Bone resorption parameters including osteoclast surface per bone surface (Oc.S/BS) and osteoclast number per bone surface (N.Oc/BS) of each sagittal section. D The area analyzed for Rankl + osteocyte percentage is indicated in the box in green. E Representative images of RANKL-positive osteocyte lacunes. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate RANKL-positive osteocyte lacunes. Red arrows indicate osteocytes with no RANKL expression. Red bars in high-power images indicate scale bars (50 μm). F The Rankl. + osteocyte percentage was qualitatively assessed in each group. Data are expressed as mean ± SD, analyzed by ANOVA followed by Tukey’s post hoc test, showing all data points. * p < 0.05, ** p < 0.01, *** p < 0.001. The number of samples are indicated at the bottom of each figure and in Supplementary Tables 3 and 4
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    HMW-HA downregulated osteoclastic bone resorption in ovariectomized mice through the downregulation of <t>RANKL-expressing</t> osteocytes. A The area analyzed for osteoclast parameters is indicated in the box in yellow. B Representative images of TRAP staining. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate osteoclasts. Red bars in high-power images indicate scale bars (50 μm). C Bone resorption parameters including osteoclast surface per bone surface (Oc.S/BS) and osteoclast number per bone surface (N.Oc/BS) of each sagittal section. D The area analyzed for Rankl + osteocyte percentage is indicated in the box in green. E Representative images of RANKL-positive osteocyte lacunes. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate RANKL-positive osteocyte lacunes. Red arrows indicate osteocytes with no RANKL expression. Red bars in high-power images indicate scale bars (50 μm). F The Rankl. + osteocyte percentage was qualitatively assessed in each group. Data are expressed as mean ± SD, analyzed by ANOVA followed by Tukey’s post hoc test, showing all data points. * p < 0.05, ** p < 0.01, *** p < 0.001. The number of samples are indicated at the bottom of each figure and in Supplementary Tables 3 and 4
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    HMW-HA downregulated osteoclastic bone resorption in ovariectomized mice through the downregulation of <t>RANKL-expressing</t> osteocytes. A The area analyzed for osteoclast parameters is indicated in the box in yellow. B Representative images of TRAP staining. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate osteoclasts. Red bars in high-power images indicate scale bars (50 μm). C Bone resorption parameters including osteoclast surface per bone surface (Oc.S/BS) and osteoclast number per bone surface (N.Oc/BS) of each sagittal section. D The area analyzed for Rankl + osteocyte percentage is indicated in the box in green. E Representative images of RANKL-positive osteocyte lacunes. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate RANKL-positive osteocyte lacunes. Red arrows indicate osteocytes with no RANKL expression. Red bars in high-power images indicate scale bars (50 μm). F The Rankl. + osteocyte percentage was qualitatively assessed in each group. Data are expressed as mean ± SD, analyzed by ANOVA followed by Tukey’s post hoc test, showing all data points. * p < 0.05, ** p < 0.01, *** p < 0.001. The number of samples are indicated at the bottom of each figure and in Supplementary Tables 3 and 4
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    Santa Cruz Biotechnology rabbit anti mouse rankl polyclonal igg
    Figure 4. Effects of Sema4D on the formation and activity of osteoclasts in vitro. (A) BMMs were cultured with <t>RANKL</t> and M-CSF in the presence or absence of Sema4D. The number of TRAP-positive multinucleated cells in each well was counted. (B) BMMs were cultured on hydroxyapatite-coated plates. The area of pits on the plates was quantified by ImageJ. (C) ST-2 cells and primary mouse osteoblasts were cultured with Sema4D. RANKL expression was examined by immunoblot analysis. (D) BMMs were cultured without RANKL with M-CSF in the presence or absence of Sema4D (100 ng/ml) and OPG. The number of TRAP-positive multinucleated cells in each well was counted. All experiments were repeated three times. Data are the mean ± SD of triplicates from a typical experiment. *p<0.05.
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    Image Search Results


    HMW-HA downregulated osteoclastic bone resorption in ovariectomized mice through the downregulation of RANKL-expressing osteocytes. A The area analyzed for osteoclast parameters is indicated in the box in yellow. B Representative images of TRAP staining. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate osteoclasts. Red bars in high-power images indicate scale bars (50 μm). C Bone resorption parameters including osteoclast surface per bone surface (Oc.S/BS) and osteoclast number per bone surface (N.Oc/BS) of each sagittal section. D The area analyzed for Rankl + osteocyte percentage is indicated in the box in green. E Representative images of RANKL-positive osteocyte lacunes. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate RANKL-positive osteocyte lacunes. Red arrows indicate osteocytes with no RANKL expression. Red bars in high-power images indicate scale bars (50 μm). F The Rankl. + osteocyte percentage was qualitatively assessed in each group. Data are expressed as mean ± SD, analyzed by ANOVA followed by Tukey’s post hoc test, showing all data points. * p < 0.05, ** p < 0.01, *** p < 0.001. The number of samples are indicated at the bottom of each figure and in Supplementary Tables 3 and 4

    Journal: BMC Musculoskeletal Disorders

    Article Title: High molecular weight hyaluronic acid alleviates ovariectomy-induced bone loss in mice

    doi: 10.1186/s12891-024-08161-y

    Figure Lengend Snippet: HMW-HA downregulated osteoclastic bone resorption in ovariectomized mice through the downregulation of RANKL-expressing osteocytes. A The area analyzed for osteoclast parameters is indicated in the box in yellow. B Representative images of TRAP staining. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate osteoclasts. Red bars in high-power images indicate scale bars (50 μm). C Bone resorption parameters including osteoclast surface per bone surface (Oc.S/BS) and osteoclast number per bone surface (N.Oc/BS) of each sagittal section. D The area analyzed for Rankl + osteocyte percentage is indicated in the box in green. E Representative images of RANKL-positive osteocyte lacunes. Low-power images boxed in red are enlarged and presented in each panel. Black arrows indicate RANKL-positive osteocyte lacunes. Red arrows indicate osteocytes with no RANKL expression. Red bars in high-power images indicate scale bars (50 μm). F The Rankl. + osteocyte percentage was qualitatively assessed in each group. Data are expressed as mean ± SD, analyzed by ANOVA followed by Tukey’s post hoc test, showing all data points. * p < 0.05, ** p < 0.01, *** p < 0.001. The number of samples are indicated at the bottom of each figure and in Supplementary Tables 3 and 4

    Article Snippet: Rabbit anti-mouse RANKL polyclonal antibody (cat#GTX32834) was purchased from Funakoshi (Tokyo, Japan).

    Techniques: Expressing, Staining

    Removal of HMW-HA from estrogen-deficient culture medium increased the RANKL expression in ST2 cells. A Experimental plan. Three hundred thousand cells were incubated for 12 h in RPMI-1640 medium. After cells were attached to the dishes, culture media were replaced with (I) charcoal-stripped FBS and (II) charcoal-stripped FBS with 100 nM of hyaluronidase for 12 h or 24 h. B , C Relative expression of RANKL and OPG in the presence or absence of hyaluronidase at 12 and 24 h. Colorful lines are associated with each 12 and 24 h samples. D Average ratio of RANKL mRNA to OPG mRNA in the presence or absence of hyaluronidase. Data are expressed as mean ± SD, analyzed by Wilcoxon signed-rank test ( B , C ), Wilcoxon rank-sum test ( D ), showing all data points. * p < 0.05. ns, not significant. n = 6 per group. Numerical data are presented in Supplementary Table 6

    Journal: BMC Musculoskeletal Disorders

    Article Title: High molecular weight hyaluronic acid alleviates ovariectomy-induced bone loss in mice

    doi: 10.1186/s12891-024-08161-y

    Figure Lengend Snippet: Removal of HMW-HA from estrogen-deficient culture medium increased the RANKL expression in ST2 cells. A Experimental plan. Three hundred thousand cells were incubated for 12 h in RPMI-1640 medium. After cells were attached to the dishes, culture media were replaced with (I) charcoal-stripped FBS and (II) charcoal-stripped FBS with 100 nM of hyaluronidase for 12 h or 24 h. B , C Relative expression of RANKL and OPG in the presence or absence of hyaluronidase at 12 and 24 h. Colorful lines are associated with each 12 and 24 h samples. D Average ratio of RANKL mRNA to OPG mRNA in the presence or absence of hyaluronidase. Data are expressed as mean ± SD, analyzed by Wilcoxon signed-rank test ( B , C ), Wilcoxon rank-sum test ( D ), showing all data points. * p < 0.05. ns, not significant. n = 6 per group. Numerical data are presented in Supplementary Table 6

    Article Snippet: Rabbit anti-mouse RANKL polyclonal antibody (cat#GTX32834) was purchased from Funakoshi (Tokyo, Japan).

    Techniques: Expressing, Incubation

    Figure 4. Effects of Sema4D on the formation and activity of osteoclasts in vitro. (A) BMMs were cultured with RANKL and M-CSF in the presence or absence of Sema4D. The number of TRAP-positive multinucleated cells in each well was counted. (B) BMMs were cultured on hydroxyapatite-coated plates. The area of pits on the plates was quantified by ImageJ. (C) ST-2 cells and primary mouse osteoblasts were cultured with Sema4D. RANKL expression was examined by immunoblot analysis. (D) BMMs were cultured without RANKL with M-CSF in the presence or absence of Sema4D (100 ng/ml) and OPG. The number of TRAP-positive multinucleated cells in each well was counted. All experiments were repeated three times. Data are the mean ± SD of triplicates from a typical experiment. *p<0.05.

    Journal: International journal of oncology

    Article Title: Semaphorin 4D promotes bone invasion in head and neck squamous cell carcinoma.

    doi: 10.3892/ijo.2017.4050

    Figure Lengend Snippet: Figure 4. Effects of Sema4D on the formation and activity of osteoclasts in vitro. (A) BMMs were cultured with RANKL and M-CSF in the presence or absence of Sema4D. The number of TRAP-positive multinucleated cells in each well was counted. (B) BMMs were cultured on hydroxyapatite-coated plates. The area of pits on the plates was quantified by ImageJ. (C) ST-2 cells and primary mouse osteoblasts were cultured with Sema4D. RANKL expression was examined by immunoblot analysis. (D) BMMs were cultured without RANKL with M-CSF in the presence or absence of Sema4D (100 ng/ml) and OPG. The number of TRAP-positive multinucleated cells in each well was counted. All experiments were repeated three times. Data are the mean ± SD of triplicates from a typical experiment. *p<0.05.

    Article Snippet: The membranes were blocked with 2% non-fat dry milk in TBS overnight at 4 ̊C and then incubated with rabbit anti-human Sema4D polyclonal IgG, rabbit anti-human Plexin-B1 polyclonal IgG (Abcam) or rabbit anti-mouse RANKL polyclonal IgG (Santa Cruz Biotechnology, Santa Cruz, CA, USA) antibodies used at a 1:200 dilution.

    Techniques: Activity Assay, In Vitro, Cell Culture, Expressing, Western Blot

    Figure 6. Role of Sema4D in bone invasion in HNSCC. IGF-I, which is released from bone, increases Sema4D secretion in HNSCC cells. Sema4D acts on HNSCC cells in an autocrine manner, which enhances cell activi- ties. Sema4D also regulated RANKL expression in osteoblasts stimulating osteoclastgenesis.

    Journal: International journal of oncology

    Article Title: Semaphorin 4D promotes bone invasion in head and neck squamous cell carcinoma.

    doi: 10.3892/ijo.2017.4050

    Figure Lengend Snippet: Figure 6. Role of Sema4D in bone invasion in HNSCC. IGF-I, which is released from bone, increases Sema4D secretion in HNSCC cells. Sema4D acts on HNSCC cells in an autocrine manner, which enhances cell activi- ties. Sema4D also regulated RANKL expression in osteoblasts stimulating osteoclastgenesis.

    Article Snippet: The membranes were blocked with 2% non-fat dry milk in TBS overnight at 4 ̊C and then incubated with rabbit anti-human Sema4D polyclonal IgG, rabbit anti-human Plexin-B1 polyclonal IgG (Abcam) or rabbit anti-mouse RANKL polyclonal IgG (Santa Cruz Biotechnology, Santa Cruz, CA, USA) antibodies used at a 1:200 dilution.

    Techniques: Expressing