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goat anti rabbit type i collagen antibody  (SouthernBiotech)


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    SouthernBiotech goat anti rabbit type i collagen antibody
    The effect of CoQ10 on the osteoblastic bone formation in ORX mice. (A) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained for HE. (B) The number of osteoblasts (N.Ob) per mm2 trabecular area (T. Area) was measured and presented. (C) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained immunohistochemically for <t>type</t> <t>I</t> <t>collagen.</t> (D) The percentage of the Col I-positive area was measured and presented by image analysis (%). Real-time RT-PCR was performed on bone tissue extracts from 48-week-old mice of each group. Gene expression of (E) OPG, (F) RUNX2 and (G) OCN are shown. Messenger RNA expression, assessed by real-time RT-PCR analysis, was calculated as a ratio to the GAPDH mRNA level and expressed relative to levels in sham mice. Data are presented as the mean ± SEM of determinations, each data point is the mean of five specimens. *P < 0.05, ***P < 0.001, versus sham mice; #P < 0.05, ##P < 0.01 versus ORX mice.
    Goat Anti Rabbit Type I Collagen Antibody, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 56 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti rabbit type i collagen antibody/product/SouthernBiotech
    Average 93 stars, based on 56 article reviews
    goat anti rabbit type i collagen antibody - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "CoQ10 suppression of oxidative stress and cell senescence increases bone mass in orchiectomized mice"

    Article Title: CoQ10 suppression of oxidative stress and cell senescence increases bone mass in orchiectomized mice

    Journal: American Journal of Translational Research

    doi:

    The effect of CoQ10 on the osteoblastic bone formation in ORX mice. (A) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained for HE. (B) The number of osteoblasts (N.Ob) per mm2 trabecular area (T. Area) was measured and presented. (C) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained immunohistochemically for type I collagen. (D) The percentage of the Col I-positive area was measured and presented by image analysis (%). Real-time RT-PCR was performed on bone tissue extracts from 48-week-old mice of each group. Gene expression of (E) OPG, (F) RUNX2 and (G) OCN are shown. Messenger RNA expression, assessed by real-time RT-PCR analysis, was calculated as a ratio to the GAPDH mRNA level and expressed relative to levels in sham mice. Data are presented as the mean ± SEM of determinations, each data point is the mean of five specimens. *P < 0.05, ***P < 0.001, versus sham mice; #P < 0.05, ##P < 0.01 versus ORX mice.
    Figure Legend Snippet: The effect of CoQ10 on the osteoblastic bone formation in ORX mice. (A) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained for HE. (B) The number of osteoblasts (N.Ob) per mm2 trabecular area (T. Area) was measured and presented. (C) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained immunohistochemically for type I collagen. (D) The percentage of the Col I-positive area was measured and presented by image analysis (%). Real-time RT-PCR was performed on bone tissue extracts from 48-week-old mice of each group. Gene expression of (E) OPG, (F) RUNX2 and (G) OCN are shown. Messenger RNA expression, assessed by real-time RT-PCR analysis, was calculated as a ratio to the GAPDH mRNA level and expressed relative to levels in sham mice. Data are presented as the mean ± SEM of determinations, each data point is the mean of five specimens. *P < 0.05, ***P < 0.001, versus sham mice; #P < 0.05, ##P < 0.01 versus ORX mice.

    Techniques Used: Staining, Quantitative RT-PCR, Expressing, RNA Expression



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    The effect of CoQ10 on the osteoblastic bone formation in ORX mice. (A) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained for HE. (B) The number of osteoblasts (N.Ob) per mm2 trabecular area (T. Area) was measured and presented. (C) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained immunohistochemically for <t>type</t> <t>I</t> <t>collagen.</t> (D) The percentage of the Col I-positive area was measured and presented by image analysis (%). Real-time RT-PCR was performed on bone tissue extracts from 48-week-old mice of each group. Gene expression of (E) OPG, (F) RUNX2 and (G) OCN are shown. Messenger RNA expression, assessed by real-time RT-PCR analysis, was calculated as a ratio to the GAPDH mRNA level and expressed relative to levels in sham mice. Data are presented as the mean ± SEM of determinations, each data point is the mean of five specimens. *P < 0.05, ***P < 0.001, versus sham mice; #P < 0.05, ##P < 0.01 versus ORX mice.
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    Image Search Results


    The effect of CoQ10 on the osteoblastic bone formation in ORX mice. (A) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained for HE. (B) The number of osteoblasts (N.Ob) per mm2 trabecular area (T. Area) was measured and presented. (C) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained immunohistochemically for type I collagen. (D) The percentage of the Col I-positive area was measured and presented by image analysis (%). Real-time RT-PCR was performed on bone tissue extracts from 48-week-old mice of each group. Gene expression of (E) OPG, (F) RUNX2 and (G) OCN are shown. Messenger RNA expression, assessed by real-time RT-PCR analysis, was calculated as a ratio to the GAPDH mRNA level and expressed relative to levels in sham mice. Data are presented as the mean ± SEM of determinations, each data point is the mean of five specimens. *P < 0.05, ***P < 0.001, versus sham mice; #P < 0.05, ##P < 0.01 versus ORX mice.

    Journal: American Journal of Translational Research

    Article Title: CoQ10 suppression of oxidative stress and cell senescence increases bone mass in orchiectomized mice

    doi:

    Figure Lengend Snippet: The effect of CoQ10 on the osteoblastic bone formation in ORX mice. (A) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained for HE. (B) The number of osteoblasts (N.Ob) per mm2 trabecular area (T. Area) was measured and presented. (C) Representative photomicrographs of paraffin sections of tibias from 48-week-old mice of each group stained immunohistochemically for type I collagen. (D) The percentage of the Col I-positive area was measured and presented by image analysis (%). Real-time RT-PCR was performed on bone tissue extracts from 48-week-old mice of each group. Gene expression of (E) OPG, (F) RUNX2 and (G) OCN are shown. Messenger RNA expression, assessed by real-time RT-PCR analysis, was calculated as a ratio to the GAPDH mRNA level and expressed relative to levels in sham mice. Data are presented as the mean ± SEM of determinations, each data point is the mean of five specimens. *P < 0.05, ***P < 0.001, versus sham mice; #P < 0.05, ##P < 0.01 versus ORX mice.

    Article Snippet: Immunohistochemical staining was carried out for type I collagen, β-galactosidase (β-gal) and p16 INK4a using the avidin-biotin-peroxidase complex technique with affinity-purified goat anti-rabbit type I collagen antibody (Southern Biotechnology Associates, Birmingham, AL, USA), β-gal (Santa Cruz Biotechnology, Santa Cruz, CA, USA) and p16 INK4a (Abcam, MA, USA) following previously-described methods [ 4 ].

    Techniques: Staining, Quantitative RT-PCR, Expressing, RNA Expression