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rabbit polyclonal anti sparc  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit polyclonal anti sparc

    Rabbit Polyclonal Anti Sparc, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 63 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti sparc/product/Cell Signaling Technology Inc
    Average 94 stars, based on 63 article reviews
    rabbit polyclonal anti sparc - by Bioz Stars, 2026-01
    94/100 stars

    Images

    1) Product Images from "PAI-1 uncouples integrin-β1 from restrain by membrane-bound β-catenin to promote collagen fibril remodeling in obesity-related neoplasms"

    Article Title: PAI-1 uncouples integrin-β1 from restrain by membrane-bound β-catenin to promote collagen fibril remodeling in obesity-related neoplasms

    Journal: Cell reports

    doi: 10.1016/j.celrep.2024.114527


    Figure Legend Snippet:

    Techniques Used: Recombinant, Membrane, Cell Culture, Reverse Transcription, SYBR Green Assay, Clinical Proteomics, Protein Extraction, Extraction, Bicinchoninic Acid Protein Assay, In Situ, Blocking Assay, Migration, shRNA, Control, Software, Pyromark Assay, Western Blot, Simple Western



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    Western blot analyses of <t>SPARC-</t> (upper panel), claudin-6- (middle panel), and CEP55 expression in whole cell extracts of 16HBE14o − cells upon exposure for 0, 12, 24, or 36 h to cylindrospermopsin (1 µmol/L—yellow squares; 2.5 µmol/L—orange triangles; 5 µmol/L—red dots) or vehicle (0.1% methanol—green diamonds). Data are presented as ratios of densities of antibody-labeled bands of the respective proteins and those of β-actin (internal standard). Means ± S.D., n = 4–10 biological replicates. Significant differences inmeans compared with those of the respective vehicle controls: *— p < 0.05; **— p < 0.01; ***— p < 0.001.
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    Image Search Results


    Journal: Cell reports

    Article Title: PAI-1 uncouples integrin-β1 from restrain by membrane-bound β-catenin to promote collagen fibril remodeling in obesity-related neoplasms

    doi: 10.1016/j.celrep.2024.114527

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal anti-SPARC , Cell Signaling Technology , Cat# 5420S; RRID: AB_10692794.

    Techniques: Recombinant, Membrane, Cell Culture, Reverse Transcription, SYBR Green Assay, Clinical Proteomics, Protein Extraction, Extraction, Bicinchoninic Acid Protein Assay, In Situ, Blocking Assay, Migration, shRNA, Control, Software, Pyromark Assay, Western Blot, Simple Western

    Fig.1. An immunohistochemical method for monitoring the expression of the SPARC in femur preparations. Weak and strong expression of SPARC is shown in the osteoblasts on the surface of trabecule and in the osteocytes (brown staining). Mag. x 100. (Ob-osteoblasts, O-osteocytes, BM- bone marrow, T-trabeculae, F-fatty degeneration).

    Journal: Journal of IMAB - Annual Proceeding (Scientific Papers)

    Article Title: SUPPLEMENT 12 SEEC & 32 IMAB, Section Varia

    doi: 10.5272/jimab.2022supplement3

    Figure Lengend Snippet: Fig.1. An immunohistochemical method for monitoring the expression of the SPARC in femur preparations. Weak and strong expression of SPARC is shown in the osteoblasts on the surface of trabecule and in the osteocytes (brown staining). Mag. x 100. (Ob-osteoblasts, O-osteocytes, BM- bone marrow, T-trabeculae, F-fatty degeneration).

    Article Snippet: SPARC antibody (H-90) rabbit polyclonal IgG and COL-1A antibody (COL-1) mouse monoclonal IgG were used for immunohistochemical study (IHH), according to the manufacturer's instructions (Santa Cruz USA and Scytek kits).

    Techniques: Immunohistochemical staining, Expressing, Staining

    Immunocytochemical analysis of characteristic bone derived proteins. After 7 days extracellular expression of collagen I and osteonectin is evident on all different surfaces examined. Scattered expression of osteocalcin is demonstrated (magnification 20-fold).

    Journal: Head & Face Medicine

    Article Title: Behavior of osteoblastic cells cultured on titanium and structured zirconia surfaces

    doi: 10.1186/1746-160X-4-29

    Figure Lengend Snippet: Immunocytochemical analysis of characteristic bone derived proteins. After 7 days extracellular expression of collagen I and osteonectin is evident on all different surfaces examined. Scattered expression of osteocalcin is demonstrated (magnification 20-fold).

    Article Snippet: After incubation for 7, 14, or 28 days at 37°C in an atmosphere of 5% CO 2 in the High GEM medium, primary antibodies were used according to the manufacturers' instructions: rabbit polyclonal anti-collagen I (Biotrend, Cologne, Germany), Mouse monoclonal anti-osteocalcin (TaKaRa Bio, MoBiTec, Goettingen, Germany) and rabbit polyclonal anti-osteonectin (SPARC; Chemicon Millipore GmbH, Schwalbach, Germany).

    Techniques: Derivative Assay, Expressing

    After 28 days expression of collagen I, osteocalcin and osteonectin is still evident on all different surfaces examined. Minimally denser accumulation of reticular collagen fibrils on zirconia surfaces as compared to titanium surfaces are observed (magnification 20-fold).

    Journal: Head & Face Medicine

    Article Title: Behavior of osteoblastic cells cultured on titanium and structured zirconia surfaces

    doi: 10.1186/1746-160X-4-29

    Figure Lengend Snippet: After 28 days expression of collagen I, osteocalcin and osteonectin is still evident on all different surfaces examined. Minimally denser accumulation of reticular collagen fibrils on zirconia surfaces as compared to titanium surfaces are observed (magnification 20-fold).

    Article Snippet: After incubation for 7, 14, or 28 days at 37°C in an atmosphere of 5% CO 2 in the High GEM medium, primary antibodies were used according to the manufacturers' instructions: rabbit polyclonal anti-collagen I (Biotrend, Cologne, Germany), Mouse monoclonal anti-osteocalcin (TaKaRa Bio, MoBiTec, Goettingen, Germany) and rabbit polyclonal anti-osteonectin (SPARC; Chemicon Millipore GmbH, Schwalbach, Germany).

    Techniques: Expressing

    Western blot analyses of SPARC- (upper panel), claudin-6- (middle panel), and CEP55 expression in whole cell extracts of 16HBE14o − cells upon exposure for 0, 12, 24, or 36 h to cylindrospermopsin (1 µmol/L—yellow squares; 2.5 µmol/L—orange triangles; 5 µmol/L—red dots) or vehicle (0.1% methanol—green diamonds). Data are presented as ratios of densities of antibody-labeled bands of the respective proteins and those of β-actin (internal standard). Means ± S.D., n = 4–10 biological replicates. Significant differences inmeans compared with those of the respective vehicle controls: *— p < 0.05; **— p < 0.01; ***— p < 0.001.

    Journal: Toxins

    Article Title: Target Mechanisms of the Cyanotoxin Cylindrospermopsin in Immortalized Human Airway Epithelial Cells

    doi: 10.3390/toxins14110785

    Figure Lengend Snippet: Western blot analyses of SPARC- (upper panel), claudin-6- (middle panel), and CEP55 expression in whole cell extracts of 16HBE14o − cells upon exposure for 0, 12, 24, or 36 h to cylindrospermopsin (1 µmol/L—yellow squares; 2.5 µmol/L—orange triangles; 5 µmol/L—red dots) or vehicle (0.1% methanol—green diamonds). Data are presented as ratios of densities of antibody-labeled bands of the respective proteins and those of β-actin (internal standard). Means ± S.D., n = 4–10 biological replicates. Significant differences inmeans compared with those of the respective vehicle controls: *— p < 0.05; **— p < 0.01; ***— p < 0.001.

    Article Snippet: The rabbit polyclonal anti-SPARC antibody was obtained from Cell Signaling Technologies (Frankfurt/M., Germany).

    Techniques: Western Blot, Expressing, Labeling