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rnoggin  (R&D Systems)


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    Structured Review

    R&D Systems rnoggin
    BMP signaling inhibition reduced calcification and promoted regeneration (A) Experimental protocol for analyzing animals treated with <t>rNoggin</t> or PBS. (B) mRNA expression levels of Id1 (3dpi) and Runx2 (5dpi) as detected by qPCR in NTX-injured muscles subsequently treated with PBS or rNoggin ( n = 4). (C) Alizarin Red and H.E. staining of TA muscles at 5 days post-NTX injury in WT mice treated with PBS or rNoggin. (D and E) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with PBS ( n = 4) or rNoggin at 5 dpi ( n = 5), respectively (3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in NTX-injured muscles treated with PBS or rNoggin at 5 dpi ( n = 4). (G) Experimental protocol for analyzing animals treated with LDN-193189 or vehicle. (H) mRNA expression levels of Id1 and Runx2 as detected by qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 3 dpi ( n = 4). (I) Alizarin Red and H.E staining of TA muscles at 5 days post-NTX injury in WT mice treated with either vehicle or LDN-193189. (J and K) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi, respectively ( n = 5, 3 images per mouse). (L) Quantitation of the relative expression of Myog and Myh3 by RT-qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi ( n = 4). (M) The Rotarod test shows the faster recovery of muscle function in mice treated with LDN-193189 ( n = 6/7). (N) The ratio of injured TA/uninjured TA/Quadriceps weight to BW at 12 dpi from mice treated with LDN-193189 ( n = 6). Data are expressed as the mean ± SD in all panels. ∗ p < 0.05, ∗∗ p < 0.01. Scale bars: in (C) and (I), upper, 200 μm; below, 50 μm. See also
    Rnoggin, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 153 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rnoggin/Recombinant+Mouse+Noggin+Protein/pmc12221681-326-0-4
    Average 95 stars, based on 153 article reviews
    rnoggin - by Bioz Stars, 2026-09
    95/100 stars

    Images

    1) Product Images from "Identification of novel macrophages and bone morphogenetic protein signals causing ectopic calcification and impairing muscle regeneration"

    Article Title: Identification of novel macrophages and bone morphogenetic protein signals causing ectopic calcification and impairing muscle regeneration

    Journal: iScience

    doi: 10.1016/j.isci.2025.112841

    BMP signaling inhibition reduced calcification and promoted regeneration (A) Experimental protocol for analyzing animals treated with rNoggin or PBS. (B) mRNA expression levels of Id1 (3dpi) and Runx2 (5dpi) as detected by qPCR in NTX-injured muscles subsequently treated with PBS or rNoggin ( n = 4). (C) Alizarin Red and H.E. staining of TA muscles at 5 days post-NTX injury in WT mice treated with PBS or rNoggin. (D and E) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with PBS ( n = 4) or rNoggin at 5 dpi ( n = 5), respectively (3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in NTX-injured muscles treated with PBS or rNoggin at 5 dpi ( n = 4). (G) Experimental protocol for analyzing animals treated with LDN-193189 or vehicle. (H) mRNA expression levels of Id1 and Runx2 as detected by qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 3 dpi ( n = 4). (I) Alizarin Red and H.E staining of TA muscles at 5 days post-NTX injury in WT mice treated with either vehicle or LDN-193189. (J and K) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi, respectively ( n = 5, 3 images per mouse). (L) Quantitation of the relative expression of Myog and Myh3 by RT-qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi ( n = 4). (M) The Rotarod test shows the faster recovery of muscle function in mice treated with LDN-193189 ( n = 6/7). (N) The ratio of injured TA/uninjured TA/Quadriceps weight to BW at 12 dpi from mice treated with LDN-193189 ( n = 6). Data are expressed as the mean ± SD in all panels. ∗ p < 0.05, ∗∗ p < 0.01. Scale bars: in (C) and (I), upper, 200 μm; below, 50 μm. See also
    Figure Legend Snippet: BMP signaling inhibition reduced calcification and promoted regeneration (A) Experimental protocol for analyzing animals treated with rNoggin or PBS. (B) mRNA expression levels of Id1 (3dpi) and Runx2 (5dpi) as detected by qPCR in NTX-injured muscles subsequently treated with PBS or rNoggin ( n = 4). (C) Alizarin Red and H.E. staining of TA muscles at 5 days post-NTX injury in WT mice treated with PBS or rNoggin. (D and E) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with PBS ( n = 4) or rNoggin at 5 dpi ( n = 5), respectively (3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in NTX-injured muscles treated with PBS or rNoggin at 5 dpi ( n = 4). (G) Experimental protocol for analyzing animals treated with LDN-193189 or vehicle. (H) mRNA expression levels of Id1 and Runx2 as detected by qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 3 dpi ( n = 4). (I) Alizarin Red and H.E staining of TA muscles at 5 days post-NTX injury in WT mice treated with either vehicle or LDN-193189. (J and K) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi, respectively ( n = 5, 3 images per mouse). (L) Quantitation of the relative expression of Myog and Myh3 by RT-qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi ( n = 4). (M) The Rotarod test shows the faster recovery of muscle function in mice treated with LDN-193189 ( n = 6/7). (N) The ratio of injured TA/uninjured TA/Quadriceps weight to BW at 12 dpi from mice treated with LDN-193189 ( n = 6). Data are expressed as the mean ± SD in all panels. ∗ p < 0.05, ∗∗ p < 0.01. Scale bars: in (C) and (I), upper, 200 μm; below, 50 μm. See also

    Techniques Used: Inhibition, Expressing, Muscles, Staining, Quantitation Assay, Quantitative RT-PCR

    BMP signaling regulated ectopic calcification in Csf1r cKO mice (A) The expression of Id1 and Runx2 via qPCR at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS and rNoggin ( n = 4). (B) Alizarin Red and H.E. staining of TA muscles at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS or rNoggin. (C–E) Quantification of the area of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with PBS and rNoggin at 5 dpi, respectively ( n = 5, 3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with PBS or rNoggin at 5 dpi ( n = 4). (G) The expression of Id1 and Runx2 via qPCR at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle and LDN-193189 ( n = 4). (H) Alizarin Red and H.E. staining of TA muscles at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle or LDN-193189. (I–K) Quantification of the areas of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with vehicle and LDN-193189 at 5 dpi, respectively ( n = 4, 3 images per mouse). (L) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with vehicle or LDN-193189 at 5 dpi ( n = 4). Data are expressed as the mean ± SD in all panels. Scale bars: in (B) and (H), upper, 200 μm; below, 50 μm. See also
    Figure Legend Snippet: BMP signaling regulated ectopic calcification in Csf1r cKO mice (A) The expression of Id1 and Runx2 via qPCR at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS and rNoggin ( n = 4). (B) Alizarin Red and H.E. staining of TA muscles at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS or rNoggin. (C–E) Quantification of the area of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with PBS and rNoggin at 5 dpi, respectively ( n = 5, 3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with PBS or rNoggin at 5 dpi ( n = 4). (G) The expression of Id1 and Runx2 via qPCR at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle and LDN-193189 ( n = 4). (H) Alizarin Red and H.E. staining of TA muscles at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle or LDN-193189. (I–K) Quantification of the areas of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with vehicle and LDN-193189 at 5 dpi, respectively ( n = 4, 3 images per mouse). (L) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with vehicle or LDN-193189 at 5 dpi ( n = 4). Data are expressed as the mean ± SD in all panels. Scale bars: in (B) and (H), upper, 200 μm; below, 50 μm. See also

    Techniques Used: Expressing, Staining, Muscles, Quantitation Assay, Quantitative RT-PCR

    Related Articles

    other:

    Article Title: GPR43 mediates microbiota metabolite SCFA regulation of antimicrobial peptide expression in intestinal epithelial cells via activation of mTOR and STAT3
    Article Snippet: The resulting pellet containing detached crypts was re-suspended in Matrigel (BD Bioscience) with 0.5μg/ml rEGF (R&D Systems2028-EG), 1μg/ml rNoggin (R&D Systems1967-NG/CF), 5μg/ml rR-spondin (R&D Systems 3474-RS), and 1μg/ml rWnt3a (R&D Systems 35036-WN/CF).

    Transduction:

    Article Title: Reprogramming efficiency and quality of induced Pluripotent Stem Cells (iPSCs) generated from muscle-derived fibroblasts of mdx mice at different ages
    Article Snippet: .. Two weeks after transduction, ES-like colonies were picked up and expanded. iPSCs were also maintained in the presence of valproic acid (VPA) (0.5 mM) (Sigma), Bix01294 (1 mM) (Stemgent), RG108 (1 mM) (Stemgent), PD0325901 (1 mM) (Stemgent), CHIR99021 (3 mM) (Stemgent), SB431542 (2.5 mg/ml) (Sigma), recombinant (r) BMP-7 (100 ng/ml) (R&D Systems), recombinant BMP-4 (100 ng/ml) (Stemgent), rNoggin (100 ng/ml)(R&D Systems), rTGF-β1 (100 ng/ml) (Stemgent), mouse rBMP-1a/ALK-3 Fc chimera protein (50 ng/ml), (R&D systems), human rBMPR-1b/ALK-6 Fc chimera protein (50 ng/ml) (R&D systems), or mouse sTGF-β RII Fc chimera protein (50 ng/ml) (R&D Systems). .. Total RNA was extracted from cells using MicroRNeasy Kit (Qiagen).

    Recombinant:

    Article Title: Reprogramming efficiency and quality of induced Pluripotent Stem Cells (iPSCs) generated from muscle-derived fibroblasts of mdx mice at different ages
    Article Snippet: .. Two weeks after transduction, ES-like colonies were picked up and expanded. iPSCs were also maintained in the presence of valproic acid (VPA) (0.5 mM) (Sigma), Bix01294 (1 mM) (Stemgent), RG108 (1 mM) (Stemgent), PD0325901 (1 mM) (Stemgent), CHIR99021 (3 mM) (Stemgent), SB431542 (2.5 mg/ml) (Sigma), recombinant (r) BMP-7 (100 ng/ml) (R&D Systems), recombinant BMP-4 (100 ng/ml) (Stemgent), rNoggin (100 ng/ml)(R&D Systems), rTGF-β1 (100 ng/ml) (Stemgent), mouse rBMP-1a/ALK-3 Fc chimera protein (50 ng/ml), (R&D systems), human rBMPR-1b/ALK-6 Fc chimera protein (50 ng/ml) (R&D systems), or mouse sTGF-β RII Fc chimera protein (50 ng/ml) (R&D Systems). .. Total RNA was extracted from cells using MicroRNeasy Kit (Qiagen).



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    BMP signaling inhibition reduced calcification and promoted regeneration (A) Experimental protocol for analyzing animals treated with <t>rNoggin</t> or PBS. (B) mRNA expression levels of Id1 (3dpi) and Runx2 (5dpi) as detected by qPCR in NTX-injured muscles subsequently treated with PBS or rNoggin ( n = 4). (C) Alizarin Red and H.E. staining of TA muscles at 5 days post-NTX injury in WT mice treated with PBS or rNoggin. (D and E) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with PBS ( n = 4) or rNoggin at 5 dpi ( n = 5), respectively (3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in NTX-injured muscles treated with PBS or rNoggin at 5 dpi ( n = 4). (G) Experimental protocol for analyzing animals treated with LDN-193189 or vehicle. (H) mRNA expression levels of Id1 and Runx2 as detected by qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 3 dpi ( n = 4). (I) Alizarin Red and H.E staining of TA muscles at 5 days post-NTX injury in WT mice treated with either vehicle or LDN-193189. (J and K) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi, respectively ( n = 5, 3 images per mouse). (L) Quantitation of the relative expression of Myog and Myh3 by RT-qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi ( n = 4). (M) The Rotarod test shows the faster recovery of muscle function in mice treated with LDN-193189 ( n = 6/7). (N) The ratio of injured TA/uninjured TA/Quadriceps weight to BW at 12 dpi from mice treated with LDN-193189 ( n = 6). Data are expressed as the mean ± SD in all panels. ∗ p < 0.05, ∗∗ p < 0.01. Scale bars: in (C) and (I), upper, 200 μm; below, 50 μm. See also
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    Image Search Results


    BMP signaling inhibition reduced calcification and promoted regeneration (A) Experimental protocol for analyzing animals treated with rNoggin or PBS. (B) mRNA expression levels of Id1 (3dpi) and Runx2 (5dpi) as detected by qPCR in NTX-injured muscles subsequently treated with PBS or rNoggin ( n = 4). (C) Alizarin Red and H.E. staining of TA muscles at 5 days post-NTX injury in WT mice treated with PBS or rNoggin. (D and E) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with PBS ( n = 4) or rNoggin at 5 dpi ( n = 5), respectively (3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in NTX-injured muscles treated with PBS or rNoggin at 5 dpi ( n = 4). (G) Experimental protocol for analyzing animals treated with LDN-193189 or vehicle. (H) mRNA expression levels of Id1 and Runx2 as detected by qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 3 dpi ( n = 4). (I) Alizarin Red and H.E staining of TA muscles at 5 days post-NTX injury in WT mice treated with either vehicle or LDN-193189. (J and K) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi, respectively ( n = 5, 3 images per mouse). (L) Quantitation of the relative expression of Myog and Myh3 by RT-qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi ( n = 4). (M) The Rotarod test shows the faster recovery of muscle function in mice treated with LDN-193189 ( n = 6/7). (N) The ratio of injured TA/uninjured TA/Quadriceps weight to BW at 12 dpi from mice treated with LDN-193189 ( n = 6). Data are expressed as the mean ± SD in all panels. ∗ p < 0.05, ∗∗ p < 0.01. Scale bars: in (C) and (I), upper, 200 μm; below, 50 μm. See also

    Journal: iScience

    Article Title: Identification of novel macrophages and bone morphogenetic protein signals causing ectopic calcification and impairing muscle regeneration

    doi: 10.1016/j.isci.2025.112841

    Figure Lengend Snippet: BMP signaling inhibition reduced calcification and promoted regeneration (A) Experimental protocol for analyzing animals treated with rNoggin or PBS. (B) mRNA expression levels of Id1 (3dpi) and Runx2 (5dpi) as detected by qPCR in NTX-injured muscles subsequently treated with PBS or rNoggin ( n = 4). (C) Alizarin Red and H.E. staining of TA muscles at 5 days post-NTX injury in WT mice treated with PBS or rNoggin. (D and E) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with PBS ( n = 4) or rNoggin at 5 dpi ( n = 5), respectively (3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in NTX-injured muscles treated with PBS or rNoggin at 5 dpi ( n = 4). (G) Experimental protocol for analyzing animals treated with LDN-193189 or vehicle. (H) mRNA expression levels of Id1 and Runx2 as detected by qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 3 dpi ( n = 4). (I) Alizarin Red and H.E staining of TA muscles at 5 days post-NTX injury in WT mice treated with either vehicle or LDN-193189. (J and K) Quantification of the area of calcium deposition and average CSA in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi, respectively ( n = 5, 3 images per mouse). (L) Quantitation of the relative expression of Myog and Myh3 by RT-qPCR in NTX-injured muscles treated with vehicle or LDN-193189 at 5 dpi ( n = 4). (M) The Rotarod test shows the faster recovery of muscle function in mice treated with LDN-193189 ( n = 6/7). (N) The ratio of injured TA/uninjured TA/Quadriceps weight to BW at 12 dpi from mice treated with LDN-193189 ( n = 6). Data are expressed as the mean ± SD in all panels. ∗ p < 0.05, ∗∗ p < 0.01. Scale bars: in (C) and (I), upper, 200 μm; below, 50 μm. See also

    Article Snippet: rNoggin was purchased from R&D Systems (1967-NG) and prepared as recommended.

    Techniques: Inhibition, Expressing, Muscles, Staining, Quantitation Assay, Quantitative RT-PCR

    BMP signaling regulated ectopic calcification in Csf1r cKO mice (A) The expression of Id1 and Runx2 via qPCR at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS and rNoggin ( n = 4). (B) Alizarin Red and H.E. staining of TA muscles at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS or rNoggin. (C–E) Quantification of the area of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with PBS and rNoggin at 5 dpi, respectively ( n = 5, 3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with PBS or rNoggin at 5 dpi ( n = 4). (G) The expression of Id1 and Runx2 via qPCR at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle and LDN-193189 ( n = 4). (H) Alizarin Red and H.E. staining of TA muscles at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle or LDN-193189. (I–K) Quantification of the areas of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with vehicle and LDN-193189 at 5 dpi, respectively ( n = 4, 3 images per mouse). (L) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with vehicle or LDN-193189 at 5 dpi ( n = 4). Data are expressed as the mean ± SD in all panels. Scale bars: in (B) and (H), upper, 200 μm; below, 50 μm. See also

    Journal: iScience

    Article Title: Identification of novel macrophages and bone morphogenetic protein signals causing ectopic calcification and impairing muscle regeneration

    doi: 10.1016/j.isci.2025.112841

    Figure Lengend Snippet: BMP signaling regulated ectopic calcification in Csf1r cKO mice (A) The expression of Id1 and Runx2 via qPCR at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS and rNoggin ( n = 4). (B) Alizarin Red and H.E. staining of TA muscles at 5 days post BaCl 2 injury in Csf1r cKO mice treated with PBS or rNoggin. (C–E) Quantification of the area of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with PBS and rNoggin at 5 dpi, respectively ( n = 5, 3 images per mouse). (F) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with PBS or rNoggin at 5 dpi ( n = 4). (G) The expression of Id1 and Runx2 via qPCR at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle and LDN-193189 ( n = 4). (H) Alizarin Red and H.E. staining of TA muscles at 5 days post-BaCl 2 injury in Csf1r cKO mice treated with vehicle or LDN-193189. (I–K) Quantification of the areas of calcium deposition and necrotic myofibers as well as average CSA in BaCl 2 -injured muscles in Csf1r cKO mice treated with vehicle and LDN-193189 at 5 dpi, respectively ( n = 4, 3 images per mouse). (L) Quantitation of the relative expression of Myog by RT-qPCR in BaCl 2 -injured muscles from Csf1r cKO mice treated with vehicle or LDN-193189 at 5 dpi ( n = 4). Data are expressed as the mean ± SD in all panels. Scale bars: in (B) and (H), upper, 200 μm; below, 50 μm. See also

    Article Snippet: rNoggin was purchased from R&D Systems (1967-NG) and prepared as recommended.

    Techniques: Expressing, Staining, Muscles, Quantitation Assay, Quantitative RT-PCR