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rabbit anti col ii antibody  (Proteintech)


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    Structured Review

    Proteintech rabbit anti col ii antibody
    Rabbit Anti Col Ii Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 984 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/collagen+type+ii+rabbit+polyclonal+antibody/Collagen+Type+I+Polyclonal+antibody/pm41791544-77-16-20
    Average 96 stars, based on 984 article reviews
    rabbit anti col ii antibody - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    other:

    Article Title: Chondroprotective effects of multiple PRP injections in osteoarthritis by apoptosis regulation and increased aggrecan synthesis- Immunohistochemistry based Guinea pig study.
    Article Snippet: We used collagen Type II rabbit polyclonal antibody (Proteintech) for collagen evaluation.

    Incubation:

    Article Title: Engineered mechanical dynamics in biomimetic hydrogel scaffold promotes phenotypic maintenance and cartilage formation of chondrocytes
    Article Snippet: The dedifferentiation of chondrocytes in cartilage tissue engineering (CTE) remains an unsolved challenge for the successful repair of severe articular cartilage defects.. We proposed to construct a mechanoactive CTE scaffold, featured with an engineered capability of in situ exerting reversible mechanical stimuli by itself upon having its environment temperature varied, to address this noted issue.. For this purpose, poly(N-isopropylacrylamide) (PNIPAM) grafting and methacrylic anhydride (MA) grafting were firstly performed to modify chitosan to generate a thermo-responsive and photo-crosslinkable hydrogel (PCM), and then fragmented electrospun poly(Llactide-co-caprolactone) (PLCL) fibers were used as fillers to reinforce the PCM hydrogel and to achieve a structural resemblance to the extracellular matrix (ECM) of cartilage.



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    Thermo Fisher rabbit type ii collagen col2 polyclonal antibody pa1 26206
    Schematic illustration of electrically primed mesenchymal stem cells (epMSCs) and their chondrogenic potential and regeneration ability in articular cartilage. MSCs, mesenchymal stem cells; ES, electrical stimulation; <t>COL2,</t> type II collagen; SOX9, SRY-box transcription factor 9; ACAN, aggrecan.
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    Merck & Co rabbit polyclonal anti-collagen type ii alpha 1 (col2a1) antibody
    hASC survival and differentiation in GelMA hydrogels. ( A ) CCK8 assay of hASCs encapsulated in the GelMA hydrogel at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. ( B ) Representative confocal imaging of Dead/live fluorescence staining of hASCs in the GelMA hydrogel after 3 weeks of culture. Red cells are dead while green cells are alive. ( C ) Alcian blue staining of GelMA hydrogel after 24 h and 3 weeks of culture. ( D ) Alizarin red staining of GelMA hydrogel after 24 h and 3 weeks of culture. ( E , F ) Confocal imaging of immunofluorescence for <t>COL2A1</t> (green) and OCN (red) in hASCs encapsulated in GelMA hydrogel after 3 weeks of culture.
    Rabbit Polyclonal Anti Collagen Type Ii Alpha 1 (Col2a1) Antibody, supplied by Merck & Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Schematic illustration of electrically primed mesenchymal stem cells (epMSCs) and their chondrogenic potential and regeneration ability in articular cartilage. MSCs, mesenchymal stem cells; ES, electrical stimulation; COL2, type II collagen; SOX9, SRY-box transcription factor 9; ACAN, aggrecan.

    Journal: Biomaterials Research

    Article Title: Enhanced Chondrogenic Differentiation of Electrically Primed Human Mesenchymal Stem Cells for the Regeneration of Osteochondral Defects

    doi: 10.34133/bmr.0109

    Figure Lengend Snippet: Schematic illustration of electrically primed mesenchymal stem cells (epMSCs) and their chondrogenic potential and regeneration ability in articular cartilage. MSCs, mesenchymal stem cells; ES, electrical stimulation; COL2, type II collagen; SOX9, SRY-box transcription factor 9; ACAN, aggrecan.

    Article Snippet: TRIzol reagent and LIVE/DEAD viability/cytotoxicity kit for mammalian cells, mouse COL1 monoclonal antibody (MA1-26771), rabbit type II collagen (COL2) polyclonal antibody (PA1-26206), CD14–phycoerythrin (PE), CD34–PE, CD45–PE, CD73–PE, CD90–PE, CD105–PE, and mouse immunoglobulin G1 kappa isotype control–PE were purchased from Invitrogen (Carlsbad, California, United States).

    Techniques:

    Histological and immunohistochemical (IHC) analyses of cartilage repair in the rat model at weeks 4 and 8 after transplantation. (A) Hematoxylin and eosin (H&E), (B) Masson’s trichrome, (C) Alcian blue, and (D) Safranin-O staining images and (E) type II collagen (COL2) IHC staining images of osteochondral defects at weeks 4 and 8 after transplantation. Scale bar = 500 μm. (F) Quantitative data of cartilage regeneration according to the O’Driscoll histological cartilage repair scale with Safranin-O stain at weeks 4 and 8. An asterisk (*) denotes a statistically significant difference ( n = 5, * P < 0.05, ** P < 0.01).

    Journal: Biomaterials Research

    Article Title: Enhanced Chondrogenic Differentiation of Electrically Primed Human Mesenchymal Stem Cells for the Regeneration of Osteochondral Defects

    doi: 10.34133/bmr.0109

    Figure Lengend Snippet: Histological and immunohistochemical (IHC) analyses of cartilage repair in the rat model at weeks 4 and 8 after transplantation. (A) Hematoxylin and eosin (H&E), (B) Masson’s trichrome, (C) Alcian blue, and (D) Safranin-O staining images and (E) type II collagen (COL2) IHC staining images of osteochondral defects at weeks 4 and 8 after transplantation. Scale bar = 500 μm. (F) Quantitative data of cartilage regeneration according to the O’Driscoll histological cartilage repair scale with Safranin-O stain at weeks 4 and 8. An asterisk (*) denotes a statistically significant difference ( n = 5, * P < 0.05, ** P < 0.01).

    Article Snippet: TRIzol reagent and LIVE/DEAD viability/cytotoxicity kit for mammalian cells, mouse COL1 monoclonal antibody (MA1-26771), rabbit type II collagen (COL2) polyclonal antibody (PA1-26206), CD14–phycoerythrin (PE), CD34–PE, CD45–PE, CD73–PE, CD90–PE, CD105–PE, and mouse immunoglobulin G1 kappa isotype control–PE were purchased from Invitrogen (Carlsbad, California, United States).

    Techniques: Immunohistochemical staining, Transplantation Assay, Staining, Immunohistochemistry

    hASC survival and differentiation in GelMA hydrogels. ( A ) CCK8 assay of hASCs encapsulated in the GelMA hydrogel at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. ( B ) Representative confocal imaging of Dead/live fluorescence staining of hASCs in the GelMA hydrogel after 3 weeks of culture. Red cells are dead while green cells are alive. ( C ) Alcian blue staining of GelMA hydrogel after 24 h and 3 weeks of culture. ( D ) Alizarin red staining of GelMA hydrogel after 24 h and 3 weeks of culture. ( E , F ) Confocal imaging of immunofluorescence for COL2A1 (green) and OCN (red) in hASCs encapsulated in GelMA hydrogel after 3 weeks of culture.

    Journal: Bioengineering

    Article Title: Comparison of Bioengineered Scaffolds for the Induction of Osteochondrogenic Differentiation of Human Adipose-Derived Stem Cells

    doi: 10.3390/bioengineering11090920

    Figure Lengend Snippet: hASC survival and differentiation in GelMA hydrogels. ( A ) CCK8 assay of hASCs encapsulated in the GelMA hydrogel at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. ( B ) Representative confocal imaging of Dead/live fluorescence staining of hASCs in the GelMA hydrogel after 3 weeks of culture. Red cells are dead while green cells are alive. ( C ) Alcian blue staining of GelMA hydrogel after 24 h and 3 weeks of culture. ( D ) Alizarin red staining of GelMA hydrogel after 24 h and 3 weeks of culture. ( E , F ) Confocal imaging of immunofluorescence for COL2A1 (green) and OCN (red) in hASCs encapsulated in GelMA hydrogel after 3 weeks of culture.

    Article Snippet: Briefly, samples were incubated with rabbit polyclonal anti-collagen type II alpha 1 (COL2A1) antibody (Merck) and rabbit polyclonal anti-osteocalcin (OCN) antibody (Thermo Fisher Scientific) for 1 h at room temperature.

    Techniques: CCK-8 Assay, Imaging, Fluorescence, Staining, Immunofluorescence

    hASC survival and differentiation in PEGDA scaffold. ( A ) CCK8 assay of hASCs seeded in the PEGDA scaffold at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. T test: * p < 0.05. ( B ) Representative confocal imaging of Dead/live fluorescence staining of hASCs seeded in the PEGDA scaffold after 3 weeks of culture. ( C ) Confocal imaging of immunofluorescence for COL2A1 (green) and OCN (red) in hASCs seeded in the PEGDA scaffold after 3 weeks of culture.

    Journal: Bioengineering

    Article Title: Comparison of Bioengineered Scaffolds for the Induction of Osteochondrogenic Differentiation of Human Adipose-Derived Stem Cells

    doi: 10.3390/bioengineering11090920

    Figure Lengend Snippet: hASC survival and differentiation in PEGDA scaffold. ( A ) CCK8 assay of hASCs seeded in the PEGDA scaffold at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. T test: * p < 0.05. ( B ) Representative confocal imaging of Dead/live fluorescence staining of hASCs seeded in the PEGDA scaffold after 3 weeks of culture. ( C ) Confocal imaging of immunofluorescence for COL2A1 (green) and OCN (red) in hASCs seeded in the PEGDA scaffold after 3 weeks of culture.

    Article Snippet: Briefly, samples were incubated with rabbit polyclonal anti-collagen type II alpha 1 (COL2A1) antibody (Merck) and rabbit polyclonal anti-osteocalcin (OCN) antibody (Thermo Fisher Scientific) for 1 h at room temperature.

    Techniques: CCK-8 Assay, Imaging, Fluorescence, Staining, Immunofluorescence

    hASC survival and differentiation in celery-based scaffold. ( A ) SEM imaging of a single hASC inside a niche of the celery-based scaffold. ( B ) CCK8 assay of hASCs seeded in the celery-based scaffold at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. T test: * p < 0.05. ( C ) Representative confocal imaging of Dead/live fluorescence staining of hASCs seeded in the scaffold after 3 weeks of culture. ( D ) Confocal 3D stack and ( E ) the projection of hASC distribution inside the scaffold. ( F ) Confocal imaging of immunofluorescence for COL2A1 (green) and OCN (red) in hASCs seeded in the PEGDA scaffold after 3 weeks of culture.

    Journal: Bioengineering

    Article Title: Comparison of Bioengineered Scaffolds for the Induction of Osteochondrogenic Differentiation of Human Adipose-Derived Stem Cells

    doi: 10.3390/bioengineering11090920

    Figure Lengend Snippet: hASC survival and differentiation in celery-based scaffold. ( A ) SEM imaging of a single hASC inside a niche of the celery-based scaffold. ( B ) CCK8 assay of hASCs seeded in the celery-based scaffold at different time points (1 week intervals). Results are reported as mean ± SEM of n = 3 samples/group. T test: * p < 0.05. ( C ) Representative confocal imaging of Dead/live fluorescence staining of hASCs seeded in the scaffold after 3 weeks of culture. ( D ) Confocal 3D stack and ( E ) the projection of hASC distribution inside the scaffold. ( F ) Confocal imaging of immunofluorescence for COL2A1 (green) and OCN (red) in hASCs seeded in the PEGDA scaffold after 3 weeks of culture.

    Article Snippet: Briefly, samples were incubated with rabbit polyclonal anti-collagen type II alpha 1 (COL2A1) antibody (Merck) and rabbit polyclonal anti-osteocalcin (OCN) antibody (Thermo Fisher Scientific) for 1 h at room temperature.

    Techniques: Imaging, CCK-8 Assay, Fluorescence, Staining, Immunofluorescence