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recombinant endostatin  (MedChemExpress)


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    Structured Review

    MedChemExpress recombinant endostatin
    (A) Representative immunofluorescence images showing VEGF expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (B) Quantification of VEGF fluorescence intensity in control and SONFH groups; (C) Representative immunofluorescence images showing <t>Endostatin</t> expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (D) Quantification of Endostatin fluorescence intensity in these two groups; (E) Representative Western blotting images of MMP-2 expression in the femoral head of control and SONFH groups; (F) Quantification of MMP-2 expression in these two groups. (*P < 0.05, **P < 0.01).
    Recombinant Endostatin, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+endostatin/Collagen+alpha-1(XVIII)+chain%2FCOL18A1%2C+Mouse/pmc13089727-58-34-38
    Average 94 stars, based on 1 article reviews
    recombinant endostatin - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head"

    Article Title: MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head

    Journal: PLOS One

    doi: 10.1371/journal.pone.0346880

    (A) Representative immunofluorescence images showing VEGF expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (B) Quantification of VEGF fluorescence intensity in control and SONFH groups; (C) Representative immunofluorescence images showing Endostatin expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (D) Quantification of Endostatin fluorescence intensity in these two groups; (E) Representative Western blotting images of MMP-2 expression in the femoral head of control and SONFH groups; (F) Quantification of MMP-2 expression in these two groups. (*P < 0.05, **P < 0.01).
    Figure Legend Snippet: (A) Representative immunofluorescence images showing VEGF expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (B) Quantification of VEGF fluorescence intensity in control and SONFH groups; (C) Representative immunofluorescence images showing Endostatin expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (D) Quantification of Endostatin fluorescence intensity in these two groups; (E) Representative Western blotting images of MMP-2 expression in the femoral head of control and SONFH groups; (F) Quantification of MMP-2 expression in these two groups. (*P < 0.05, **P < 0.01).

    Techniques Used: Immunofluorescence, Expressing, Control, Fluorescence, Western Blot

    (A) Representative HE staining images of the femoral head in control, SONFH, and SONFH+Endostatin groups (scale bar = 100 μm); (B) Quantitative analysis of percentage of empty osteocyte from HE staining; (C) Representative micro-CT vascular reconstructions of the femoral head in each group; (D) Calcein staining images showing mineral apposition in each group (scale bar = 25 μm); (E) Quantitative analysis of vascular volume fraction from micro-CT angiography; (F) Quantification of mineral apposition rate (MAR) in each group. (*P < 0.05, ***P < 0.001, ****P < 0.0001).
    Figure Legend Snippet: (A) Representative HE staining images of the femoral head in control, SONFH, and SONFH+Endostatin groups (scale bar = 100 μm); (B) Quantitative analysis of percentage of empty osteocyte from HE staining; (C) Representative micro-CT vascular reconstructions of the femoral head in each group; (D) Calcein staining images showing mineral apposition in each group (scale bar = 25 μm); (E) Quantitative analysis of vascular volume fraction from micro-CT angiography; (F) Quantification of mineral apposition rate (MAR) in each group. (*P < 0.05, ***P < 0.001, ****P < 0.0001).

    Techniques Used: Staining, Control, Micro-CT

    (A) Relative mRNA levels of Endostatin in the femoral head tissues of each group; (B) Western blotting images showing Endostatin protein expression; (C) Quantification of Endostatin protein levels; (D) Representative immunofluorescence images of Endostatin expression; (E) Quantitative analysis of Endostatin immunofluorescence intensity. (*P < 0.05, **P < 0.01, ***P < 0.001).
    Figure Legend Snippet: (A) Relative mRNA levels of Endostatin in the femoral head tissues of each group; (B) Western blotting images showing Endostatin protein expression; (C) Quantification of Endostatin protein levels; (D) Representative immunofluorescence images of Endostatin expression; (E) Quantitative analysis of Endostatin immunofluorescence intensity. (*P < 0.05, **P < 0.01, ***P < 0.001).

    Techniques Used: Western Blot, Expressing, Immunofluorescence

    Related Articles

    Mouse Assay:

    Article Title: MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head
    Article Snippet: .. Mice in the SONFH+MMP-2 group received subcutaneous injections of recombinant MMP-2 (10 μg/kg; MedChemExpress, NJ, USA) every three days [ , ], while those in the SONFH+Endostatin group were administered daily subcutaneous injections of recombinant Endostatin (2 mg/kg; MedChemExpress, NJ, USA) [ ]. ..

    Recombinant:

    Article Title: MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head
    Article Snippet: .. Mice in the SONFH+MMP-2 group received subcutaneous injections of recombinant MMP-2 (10 μg/kg; MedChemExpress, NJ, USA) every three days [ , ], while those in the SONFH+Endostatin group were administered daily subcutaneous injections of recombinant Endostatin (2 mg/kg; MedChemExpress, NJ, USA) [ ]. ..



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    (A) Representative immunofluorescence images showing VEGF expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (B) Quantification of VEGF fluorescence intensity in control and SONFH groups; (C) Representative immunofluorescence images showing <t>Endostatin</t> expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (D) Quantification of Endostatin fluorescence intensity in these two groups; (E) Representative Western blotting images of MMP-2 expression in the femoral head of control and SONFH groups; (F) Quantification of MMP-2 expression in these two groups. (*P < 0.05, **P < 0.01).
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    Image Search Results


    (A) Representative immunofluorescence images showing VEGF expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (B) Quantification of VEGF fluorescence intensity in control and SONFH groups; (C) Representative immunofluorescence images showing Endostatin expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (D) Quantification of Endostatin fluorescence intensity in these two groups; (E) Representative Western blotting images of MMP-2 expression in the femoral head of control and SONFH groups; (F) Quantification of MMP-2 expression in these two groups. (*P < 0.05, **P < 0.01).

    Journal: PLOS One

    Article Title: MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head

    doi: 10.1371/journal.pone.0346880

    Figure Lengend Snippet: (A) Representative immunofluorescence images showing VEGF expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (B) Quantification of VEGF fluorescence intensity in control and SONFH groups; (C) Representative immunofluorescence images showing Endostatin expression in the femoral head of control and SONFH groups (scale bar = 100 μm); (D) Quantification of Endostatin fluorescence intensity in these two groups; (E) Representative Western blotting images of MMP-2 expression in the femoral head of control and SONFH groups; (F) Quantification of MMP-2 expression in these two groups. (*P < 0.05, **P < 0.01).

    Article Snippet: Mice in the SONFH+MMP-2 group received subcutaneous injections of recombinant MMP-2 (10 μg/kg; MedChemExpress, NJ, USA) every three days [ , ], while those in the SONFH+Endostatin group were administered daily subcutaneous injections of recombinant Endostatin (2 mg/kg; MedChemExpress, NJ, USA) [ ].

    Techniques: Immunofluorescence, Expressing, Control, Fluorescence, Western Blot

    (A) Representative HE staining images of the femoral head in control, SONFH, and SONFH+Endostatin groups (scale bar = 100 μm); (B) Quantitative analysis of percentage of empty osteocyte from HE staining; (C) Representative micro-CT vascular reconstructions of the femoral head in each group; (D) Calcein staining images showing mineral apposition in each group (scale bar = 25 μm); (E) Quantitative analysis of vascular volume fraction from micro-CT angiography; (F) Quantification of mineral apposition rate (MAR) in each group. (*P < 0.05, ***P < 0.001, ****P < 0.0001).

    Journal: PLOS One

    Article Title: MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head

    doi: 10.1371/journal.pone.0346880

    Figure Lengend Snippet: (A) Representative HE staining images of the femoral head in control, SONFH, and SONFH+Endostatin groups (scale bar = 100 μm); (B) Quantitative analysis of percentage of empty osteocyte from HE staining; (C) Representative micro-CT vascular reconstructions of the femoral head in each group; (D) Calcein staining images showing mineral apposition in each group (scale bar = 25 μm); (E) Quantitative analysis of vascular volume fraction from micro-CT angiography; (F) Quantification of mineral apposition rate (MAR) in each group. (*P < 0.05, ***P < 0.001, ****P < 0.0001).

    Article Snippet: Mice in the SONFH+MMP-2 group received subcutaneous injections of recombinant MMP-2 (10 μg/kg; MedChemExpress, NJ, USA) every three days [ , ], while those in the SONFH+Endostatin group were administered daily subcutaneous injections of recombinant Endostatin (2 mg/kg; MedChemExpress, NJ, USA) [ ].

    Techniques: Staining, Control, Micro-CT

    (A) Relative mRNA levels of Endostatin in the femoral head tissues of each group; (B) Western blotting images showing Endostatin protein expression; (C) Quantification of Endostatin protein levels; (D) Representative immunofluorescence images of Endostatin expression; (E) Quantitative analysis of Endostatin immunofluorescence intensity. (*P < 0.05, **P < 0.01, ***P < 0.001).

    Journal: PLOS One

    Article Title: MMP-2 associated imbalance of VEGF/Endostatin is linked to suppression of the PI3K/AKT/HIF-1α pathway in steroid-induced osteonecrosis of femoral head

    doi: 10.1371/journal.pone.0346880

    Figure Lengend Snippet: (A) Relative mRNA levels of Endostatin in the femoral head tissues of each group; (B) Western blotting images showing Endostatin protein expression; (C) Quantification of Endostatin protein levels; (D) Representative immunofluorescence images of Endostatin expression; (E) Quantitative analysis of Endostatin immunofluorescence intensity. (*P < 0.05, **P < 0.01, ***P < 0.001).

    Article Snippet: Mice in the SONFH+MMP-2 group received subcutaneous injections of recombinant MMP-2 (10 μg/kg; MedChemExpress, NJ, USA) every three days [ , ], while those in the SONFH+Endostatin group were administered daily subcutaneous injections of recombinant Endostatin (2 mg/kg; MedChemExpress, NJ, USA) [ ].

    Techniques: Western Blot, Expressing, Immunofluorescence

    The efficacy assessment of 154 cases of recurrent/metastatic head and neck squamous cell carcinoma patients treated with first-line PD-1 inhibitors in combination with a taxane-based chemotherapy

    Journal: World Journal of Surgical Oncology

    Article Title: The efficacy and safety of a taxane-based chemotherapy regimen combined with a PD-1 inhibitor in HNSCC: a multicenter real-world study

    doi: 10.1186/s12957-024-03644-7

    Figure Lengend Snippet: The efficacy assessment of 154 cases of recurrent/metastatic head and neck squamous cell carcinoma patients treated with first-line PD-1 inhibitors in combination with a taxane-based chemotherapy

    Article Snippet: China International Medical Exchange Foundation, Simcere Anti-Tumor Special Fund Clinical Project, Intratumoral Injection of Recombinant Human Endostatin Combined with Chemotherapy for the Treatment of Exophytic Recurrent and Metastatic Malignant Tumors of the Head and Neck, Registration Number: ChiCTR1900022364; Project Number: Z-2014-06-18384.

    Techniques:

    The progression-free survival rate of 154 cases of recurrent/metastatic head and neck squamous cell carcinoma patients treated with first-line PD-1 inhibitors in combination with a taxane-based chemotherapy

    Journal: World Journal of Surgical Oncology

    Article Title: The efficacy and safety of a taxane-based chemotherapy regimen combined with a PD-1 inhibitor in HNSCC: a multicenter real-world study

    doi: 10.1186/s12957-024-03644-7

    Figure Lengend Snippet: The progression-free survival rate of 154 cases of recurrent/metastatic head and neck squamous cell carcinoma patients treated with first-line PD-1 inhibitors in combination with a taxane-based chemotherapy

    Article Snippet: China International Medical Exchange Foundation, Simcere Anti-Tumor Special Fund Clinical Project, Intratumoral Injection of Recombinant Human Endostatin Combined with Chemotherapy for the Treatment of Exophytic Recurrent and Metastatic Malignant Tumors of the Head and Neck, Registration Number: ChiCTR1900022364; Project Number: Z-2014-06-18384.

    Techniques:

    The overall survival rate of 154 cases of recurrent/metastatic head and neck squamous cell carcinoma patients treated with first-line PD-1 inhibitors in combination with a taxane-based chemotherapy

    Journal: World Journal of Surgical Oncology

    Article Title: The efficacy and safety of a taxane-based chemotherapy regimen combined with a PD-1 inhibitor in HNSCC: a multicenter real-world study

    doi: 10.1186/s12957-024-03644-7

    Figure Lengend Snippet: The overall survival rate of 154 cases of recurrent/metastatic head and neck squamous cell carcinoma patients treated with first-line PD-1 inhibitors in combination with a taxane-based chemotherapy

    Article Snippet: China International Medical Exchange Foundation, Simcere Anti-Tumor Special Fund Clinical Project, Intratumoral Injection of Recombinant Human Endostatin Combined with Chemotherapy for the Treatment of Exophytic Recurrent and Metastatic Malignant Tumors of the Head and Neck, Registration Number: ChiCTR1900022364; Project Number: Z-2014-06-18384.

    Techniques:

    Kaplan-meier curves for univariate analysis of clinical characteristics in patients with recurrent/metastatic head and neck squamous cell carcinoma treated with pd-1 inhibitors in combination with a taxane-based chemotherapy. Note (A) : Comparison of PFS survival curves based on the presence or absence of distant metastasis; (B) : Comparison of OS survival curves based on the presence or absence of distant metastasis; (C) : Comparison of PFS survival curves based on whether subsequent radiotherapy was administered; (D) : Comparison of OS survival curves based on whether subsequent radiotherapy was administered; (E): Comparison of PFS survival curves based on whether radiotherapy was administered before recurrence/metastasis; (F) : Comparison of OS survival curves based on whether radiotherapy was administered before recurrence/metastasis;

    Journal: World Journal of Surgical Oncology

    Article Title: The efficacy and safety of a taxane-based chemotherapy regimen combined with a PD-1 inhibitor in HNSCC: a multicenter real-world study

    doi: 10.1186/s12957-024-03644-7

    Figure Lengend Snippet: Kaplan-meier curves for univariate analysis of clinical characteristics in patients with recurrent/metastatic head and neck squamous cell carcinoma treated with pd-1 inhibitors in combination with a taxane-based chemotherapy. Note (A) : Comparison of PFS survival curves based on the presence or absence of distant metastasis; (B) : Comparison of OS survival curves based on the presence or absence of distant metastasis; (C) : Comparison of PFS survival curves based on whether subsequent radiotherapy was administered; (D) : Comparison of OS survival curves based on whether subsequent radiotherapy was administered; (E): Comparison of PFS survival curves based on whether radiotherapy was administered before recurrence/metastasis; (F) : Comparison of OS survival curves based on whether radiotherapy was administered before recurrence/metastasis;

    Article Snippet: China International Medical Exchange Foundation, Simcere Anti-Tumor Special Fund Clinical Project, Intratumoral Injection of Recombinant Human Endostatin Combined with Chemotherapy for the Treatment of Exophytic Recurrent and Metastatic Malignant Tumors of the Head and Neck, Registration Number: ChiCTR1900022364; Project Number: Z-2014-06-18384.

    Techniques: Comparison

    Multifactorial analysis of progression-free survival in 154 cases of recurrent/metastatic squamous cell carcinoma of the head and neck treated with first-line pd-1 inhibitors combined with a taxane-based chemotherapy

    Journal: World Journal of Surgical Oncology

    Article Title: The efficacy and safety of a taxane-based chemotherapy regimen combined with a PD-1 inhibitor in HNSCC: a multicenter real-world study

    doi: 10.1186/s12957-024-03644-7

    Figure Lengend Snippet: Multifactorial analysis of progression-free survival in 154 cases of recurrent/metastatic squamous cell carcinoma of the head and neck treated with first-line pd-1 inhibitors combined with a taxane-based chemotherapy

    Article Snippet: China International Medical Exchange Foundation, Simcere Anti-Tumor Special Fund Clinical Project, Intratumoral Injection of Recombinant Human Endostatin Combined with Chemotherapy for the Treatment of Exophytic Recurrent and Metastatic Malignant Tumors of the Head and Neck, Registration Number: ChiCTR1900022364; Project Number: Z-2014-06-18384.

    Techniques:

    Multifactorial analysis of overall survival in 154 cases of recurrent/metastatic squamous cell carcinoma of the head and neck treated with first-line pd-1 inhibitors combined with a taxane-based chemotherapy

    Journal: World Journal of Surgical Oncology

    Article Title: The efficacy and safety of a taxane-based chemotherapy regimen combined with a PD-1 inhibitor in HNSCC: a multicenter real-world study

    doi: 10.1186/s12957-024-03644-7

    Figure Lengend Snippet: Multifactorial analysis of overall survival in 154 cases of recurrent/metastatic squamous cell carcinoma of the head and neck treated with first-line pd-1 inhibitors combined with a taxane-based chemotherapy

    Article Snippet: China International Medical Exchange Foundation, Simcere Anti-Tumor Special Fund Clinical Project, Intratumoral Injection of Recombinant Human Endostatin Combined with Chemotherapy for the Treatment of Exophytic Recurrent and Metastatic Malignant Tumors of the Head and Neck, Registration Number: ChiCTR1900022364; Project Number: Z-2014-06-18384.

    Techniques:

    The efficacy of endostar with NSCLC in previously reported studies

    Journal: BMC Cancer

    Article Title: Endostar acts as a pneumonitis protectant in patients with locally advanced non-small cell lung cancer receiving concurrent chemoradiotherapy

    doi: 10.1186/s12885-024-12001-6

    Figure Lengend Snippet: The efficacy of endostar with NSCLC in previously reported studies

    Article Snippet: Recombinant human endostatin (Endostar): In the CCRT + Endostar group, the administered dose of Endostar (Shandong Simcere-Medgenn Bio-pharmaceutical Co., LTD., trade name: Endostar, Sinopharm approved S20050088) was 7.5 mg/m 2 /day with 1–14 days of continuous administration.

    Techniques: Control

    FIGURE 2 Ad‐E improved antitumor activity in vivo. (A) In the B16F10 model, mice in the Ad‐Null and Ad‐E groups were intratumorally injected with 1 × 109 pfu empty adenovirus (Ad‐Null) or recombinant adenovirus expressing endostatin (Ad‐E), respectively, every 3 days for four injection in total. Mice in the control group received sterile saline. Data are representative of at least two independent experiments. (B) In the MC38 model, an adenovirus was intratumorally injected at a dose of 3 × 108 pfu once a week for 2 weeks. Data are representative of at least two independent experiments. (C) In the B16F10 model, 3 days after the last dose of Ad‐E therapy, mice (n = 3) were killed, and tumors were processed to analyze the proportions of CD4+ and CD8+ T cells. (D) PD‐L1 mRNA expression in tumors were detected by RT‐qPCR. *p < 0.05. **p < 0.01. ***p < 0.001. mRNA, messenger RNA; RT‐qPCR, quantitative real‐time polymerase chain reaction.

    Journal: MedComm – Oncology

    Article Title: Combining an adenovirus encoding human endostatin and PD‐1 blockade enhanced antitumor immune activity

    doi: 10.1002/mog2.21

    Figure Lengend Snippet: FIGURE 2 Ad‐E improved antitumor activity in vivo. (A) In the B16F10 model, mice in the Ad‐Null and Ad‐E groups were intratumorally injected with 1 × 109 pfu empty adenovirus (Ad‐Null) or recombinant adenovirus expressing endostatin (Ad‐E), respectively, every 3 days for four injection in total. Mice in the control group received sterile saline. Data are representative of at least two independent experiments. (B) In the MC38 model, an adenovirus was intratumorally injected at a dose of 3 × 108 pfu once a week for 2 weeks. Data are representative of at least two independent experiments. (C) In the B16F10 model, 3 days after the last dose of Ad‐E therapy, mice (n = 3) were killed, and tumors were processed to analyze the proportions of CD4+ and CD8+ T cells. (D) PD‐L1 mRNA expression in tumors were detected by RT‐qPCR. *p < 0.05. **p < 0.01. ***p < 0.001. mRNA, messenger RNA; RT‐qPCR, quantitative real‐time polymerase chain reaction.

    Article Snippet: Among the treatment protocols, empty adenoviral vectors or the recombinant adenovirus expressing endostatin was intratumorally injected at a dose of 3 × 108 pfu once a week for 2 weeks in the MC38 model or at 1 × 109 pfu twice a week for 2 weeks in the B16F10 model. IgG2a or an anti‐PD‐1 (αPD‐1) mAb (both from Bio X Cell) was intraperitoneally injected at a dose of 200 μg twice a week for 2 weeks in both MC38 and B16F10 tumor models.

    Techniques: Activity Assay, In Vivo, Injection, Recombinant, Expressing, Control, Sterility, Saline, Quantitative RT-PCR, Real-time Polymerase Chain Reaction

    Integrin-targeting therapies in clinical trials

    Journal: Signal Transduction and Targeted Therapy

    Article Title: Targeting integrin pathways: mechanisms and advances in therapy

    doi: 10.1038/s41392-022-01259-6

    Figure Lengend Snippet: Integrin-targeting therapies in clinical trials

    Article Snippet: Pegylated recombinant human endostatin , NCT01527864 , Protgen Ltd , Peptide , 2012-02-07 , α5β1 , Non-small cell lung cancer , 10 mg/m 2 QW , IV , Phase II.

    Techniques: Recombinant, Methylation, Injection, Imaging, Biomarker Discovery, Cream, Ointment, Synthesized