anti mouse  (Boster Bio)


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    Name:
    Anti Mouse IL 27 P28 Monoclonal Antibody
    Description:

    Catalog Number:
    M00857
    Price:
    399.0
    Category:
    Primary Antibodies
    Reactivity:
    Mouse
    Applications:
    WB
    Host:
    Rat
    Buy from Supplier


    Structured Review

    Boster Bio anti mouse
    Anti Mouse IL 27 P28 Monoclonal Antibody

    https://www.bioz.com/result/anti mouse/product/Boster Bio
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti mouse - by Bioz Stars, 2021-05
    94/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: 8-hydroxy-dipropylaminotetralin promotes neural plasticity in epileptic rats with depression ★
    Article Snippet: The sections were subsequently incubated in 1% bovine serum albumin to block non-specific signals. .. Following serum blocking, the sections were incubated with mouse anti-rat BrdU monoclonal antibody (1:100; Boster, Wuhan, China) in PBS containing 0.3% Triton X-100 overnight at 4°C. .. Following a PBS rinse, the sections were incubated with goat anti-mouse IgG-Cy2 (1:100; Boster) for 2 hours at room temperature.

    Incubation:

    Article Title: 8-hydroxy-dipropylaminotetralin promotes neural plasticity in epileptic rats with depression ★
    Article Snippet: The sections were subsequently incubated in 1% bovine serum albumin to block non-specific signals. .. Following serum blocking, the sections were incubated with mouse anti-rat BrdU monoclonal antibody (1:100; Boster, Wuhan, China) in PBS containing 0.3% Triton X-100 overnight at 4°C. .. Following a PBS rinse, the sections were incubated with goat anti-mouse IgG-Cy2 (1:100; Boster) for 2 hours at room temperature.

    Hydroxyproline Assay:

    Article Title: Expression of p53 in the Effects of Artesunate on Induction of Apoptosis and Inhibition of Proliferation in Rat Primary Hepatic Stellate Cells
    Article Snippet: Pronase E were purchased from Roche Diagnostics GmbH (Roche, Mannheim, GER), type IV collagenase were purchased from Sigma (St. Louis, MO, USA). .. Mouse antibody for human glial fibrillary acidic protein (GFAP), goat antibody for mouse IgG-FITC, rabbit antibody for rat desmin, goat antibody for rabbit IgG-TRITC was purchased from Wuhan Boster Bio-engineering Limited Company (Boster, Wuhan, CHN), hydroxyproline assay kit purchased from Nanjing Jiancheng Biological Engineering Institute(Jiancheng, Nanjing, CHN). .. Nuclear protein and cytoplasmic protein extraction kit, high sensitivity ECL chemiluminescence kit, HRP-labeled goat anti-mouse IgG (H+L), β-actin antibody, Annexin V-FITC/PI kits and Beyozol were purchased from Beyotime Institute of Biotechnology (Beyotime, Haimen, CHN).

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  • 96
    Boster Bio mouse monoclonal anti rabbit α sma antibody
    Schematic diagram of myofibroblast sources and differentiation. Inducing factors, e.g., transforming growth factor-β (TGF-β), mechanical stress and integrin would induce fibroblasts change into protomyofibroblasts and then transition into differentiated myofibroblasts characterized by contractile properties because of the formation of robust stress fibers containing α-smooth muscle actin <t>(α-SMA).</t>
    Mouse Monoclonal Anti Rabbit α Sma Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse monoclonal anti rabbit α sma antibody/product/Boster Bio
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse monoclonal anti rabbit α sma antibody - by Bioz Stars, 2021-05
    96/100 stars
      Buy from Supplier

    97
    Boster Bio mouse anti β actin
    Hypoxia/reoxygenation-induced changes in the protein and mRNA expression levels of COX-2 and iNOS;  β -actin was also quantified as a control. (a) The mRNA expression levels of COX-2 and iNOS were determined via real-time PCR. (b) The cellular protein expression levels of COX-2 and iNOS were analyzed via Western blot.  # P
    Mouse Anti β Actin, supplied by Boster Bio, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti β actin/product/Boster Bio
    Average 97 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse anti β actin - by Bioz Stars, 2021-05
    97/100 stars
      Buy from Supplier

    95
    Boster Bio mouse anti sma
    Identification of isolated cells. (A) As shown by flow cytometry analysis, at passage 3 (P3) after sorting, the c-kit-positive cells reached 93.4±0.95%, but were negative for the hematopoietic and endothelial antigens, CD45 (2.1±0.26%), CD31 (1.67±0.35%), CD34 (3.4±0.5%) and KDR (2.8±0.42%). As expected, they were positive for the control mesenchymal markerS, CD90 (71.6±1.55%), CD29 (93.7±1.2%), and THYE stemness marker Sca-1 (82.33±0.90%). (B) Immunofluorescence staining of the main cardiac lineages differentiated from c-kit + cells, namely (panel b) the cardiomyocyte marker, <t>TnI;</t> (panel c) the smooth muscle cell marker, <t>SMA;</t> and (panel d) the endothelial cell marker, vWF. The expression of the cardiac lineage markers (panel e) GATA-4; and (panel f) Nkx2.5 in the c-kit + cells was also analyzed. Nuclei were counterstained with DAPI.
    Mouse Anti Sma, supplied by Boster Bio, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti sma/product/Boster Bio
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse anti sma - by Bioz Stars, 2021-05
    95/100 stars
      Buy from Supplier


    Image Search Results


    Schematic diagram of myofibroblast sources and differentiation. Inducing factors, e.g., transforming growth factor-β (TGF-β), mechanical stress and integrin would induce fibroblasts change into protomyofibroblasts and then transition into differentiated myofibroblasts characterized by contractile properties because of the formation of robust stress fibers containing α-smooth muscle actin (α-SMA).

    Journal: International Journal of Molecular Medicine

    Article Title: Extracorporeal shock wave therapy with low-energy flux density inhibits hypertrophic scar formation in an animal model

    doi: 10.3892/ijmm.2018.3434

    Figure Lengend Snippet: Schematic diagram of myofibroblast sources and differentiation. Inducing factors, e.g., transforming growth factor-β (TGF-β), mechanical stress and integrin would induce fibroblasts change into protomyofibroblasts and then transition into differentiated myofibroblasts characterized by contractile properties because of the formation of robust stress fibers containing α-smooth muscle actin (α-SMA).

    Article Snippet: Specifically, tissue sections were deparaffinized in xylene and rehydrated in a series of graded ethanol and then subjected to the antigen retrieval by cooking in 0.01 M citrate buffer (pH 6.0) for 3 min. After washed with phosphate-buffered saline (PBS) briefly three times, the endogenous peroxidase activity in tissues was blocked by treating the tissue sections with 0.3% H2 O2 in 70% methanol at room temperature for 20 min and tissues sections were incubated in 10% normal goat serum at room temperature for 20 min and further incubated with a mouse anti-rabbit monoclonal PCNA antibody (cat. no. BM0104; Wuhan Boster Biological Technology, Ltd., Wuhan, China) or a mouse monoclonal anti-rabbit α-SMA antibody (cat no. BM0002; Wuhan Boster Biological Technology, Ltd.) both at 1:100 dilution at 4°C overnight.

    Techniques:

    Effects of extracorporeal shock wave therapy (ESWT) administration on modulation of proliferating cell nuclear antigen (PCNA) and α-smooth muscle actin (α-SMA) mRNA level. The animals were subjected to L-ESWT or H-ESWT for up to 5 weeks and the hypertrophic scar tissues were processed for RT-PCR analysis of (A) PCNA and (B) α-SMA mRNA.

    Journal: International Journal of Molecular Medicine

    Article Title: Extracorporeal shock wave therapy with low-energy flux density inhibits hypertrophic scar formation in an animal model

    doi: 10.3892/ijmm.2018.3434

    Figure Lengend Snippet: Effects of extracorporeal shock wave therapy (ESWT) administration on modulation of proliferating cell nuclear antigen (PCNA) and α-smooth muscle actin (α-SMA) mRNA level. The animals were subjected to L-ESWT or H-ESWT for up to 5 weeks and the hypertrophic scar tissues were processed for RT-PCR analysis of (A) PCNA and (B) α-SMA mRNA.

    Article Snippet: Specifically, tissue sections were deparaffinized in xylene and rehydrated in a series of graded ethanol and then subjected to the antigen retrieval by cooking in 0.01 M citrate buffer (pH 6.0) for 3 min. After washed with phosphate-buffered saline (PBS) briefly three times, the endogenous peroxidase activity in tissues was blocked by treating the tissue sections with 0.3% H2 O2 in 70% methanol at room temperature for 20 min and tissues sections were incubated in 10% normal goat serum at room temperature for 20 min and further incubated with a mouse anti-rabbit monoclonal PCNA antibody (cat. no. BM0104; Wuhan Boster Biological Technology, Ltd., Wuhan, China) or a mouse monoclonal anti-rabbit α-SMA antibody (cat no. BM0002; Wuhan Boster Biological Technology, Ltd.) both at 1:100 dilution at 4°C overnight.

    Techniques: Reverse Transcription Polymerase Chain Reaction

    Hypoxia/reoxygenation-induced changes in the protein and mRNA expression levels of COX-2 and iNOS;  β -actin was also quantified as a control. (a) The mRNA expression levels of COX-2 and iNOS were determined via real-time PCR. (b) The cellular protein expression levels of COX-2 and iNOS were analyzed via Western blot.  # P

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Qingkailing Suppresses the Activation of BV2 Microglial Cells by Inhibiting Hypoxia/Reoxygenation-Induced Inflammatory Responses

    doi: 10.1155/2014/696218

    Figure Lengend Snippet: Hypoxia/reoxygenation-induced changes in the protein and mRNA expression levels of COX-2 and iNOS; β -actin was also quantified as a control. (a) The mRNA expression levels of COX-2 and iNOS were determined via real-time PCR. (b) The cellular protein expression levels of COX-2 and iNOS were analyzed via Western blot. # P

    Article Snippet: The mouse anti-β -actin and HRP-labeled goat anti-rabbit IgG antibodies were purchased from Wuhan Boster Biological Technology, Ltd.

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot

    Inhibitory effects of PTF on MMP-2 and MMP-9 expression in NCI-H1703 cells. (A) Changes in the protein expression of metalloproteinases MMP-9 and MMP-2 in NCI-H1703 treated by PTF. β-Actin was used as a loading control. (B) PTF decreased MMP-2 and MMP-9 expression in NCI-H1703 cells, which was assessed via quantitative densitometry analysis. Results are represented as the mean±SD from three independent experiments. n =3, c P

    Journal: Acta Pharmacologica Sinica

    Article Title: Fructus phyllanthi tannin fraction induces apoptosis and inhibits migration and invasion of human lung squamous carcinoma cells in vitro via MAPK/MMP pathways

    doi: 10.1038/aps.2014.130

    Figure Lengend Snippet: Inhibitory effects of PTF on MMP-2 and MMP-9 expression in NCI-H1703 cells. (A) Changes in the protein expression of metalloproteinases MMP-9 and MMP-2 in NCI-H1703 treated by PTF. β-Actin was used as a loading control. (B) PTF decreased MMP-2 and MMP-9 expression in NCI-H1703 cells, which was assessed via quantitative densitometry analysis. Results are represented as the mean±SD from three independent experiments. n =3, c P

    Article Snippet: The rabbit polyclonal anti-ERK1/2, mouse monoclonal anti-β-actin, goat anti-mouse IgG, goat anti-rabbit IgG antibodies, a BCA protein assay kit, and an enhanced chemiluminescent method of Western blotting assay kit were purchased from Boster (Wuhan, China).

    Techniques: Expressing

    The effects of PTF on ERK1/2 and JNK expression in NCI-H1703 cells. (A) Total expression and phosphorylation of ERK and JNK were analyzed by Western blotting in NCI-H1703 cells treated with PTF for 24 h. β-Actin was used as a loading control. (B) The ratios of p-ERK/ERK and p-JNK/JNK were analyzed. Results are represented as the mean±SD from three independent experiments. n =3, b P

    Journal: Acta Pharmacologica Sinica

    Article Title: Fructus phyllanthi tannin fraction induces apoptosis and inhibits migration and invasion of human lung squamous carcinoma cells in vitro via MAPK/MMP pathways

    doi: 10.1038/aps.2014.130

    Figure Lengend Snippet: The effects of PTF on ERK1/2 and JNK expression in NCI-H1703 cells. (A) Total expression and phosphorylation of ERK and JNK were analyzed by Western blotting in NCI-H1703 cells treated with PTF for 24 h. β-Actin was used as a loading control. (B) The ratios of p-ERK/ERK and p-JNK/JNK were analyzed. Results are represented as the mean±SD from three independent experiments. n =3, b P

    Article Snippet: The rabbit polyclonal anti-ERK1/2, mouse monoclonal anti-β-actin, goat anti-mouse IgG, goat anti-rabbit IgG antibodies, a BCA protein assay kit, and an enhanced chemiluminescent method of Western blotting assay kit were purchased from Boster (Wuhan, China).

    Techniques: Expressing, Western Blot

    Identification of isolated cells. (A) As shown by flow cytometry analysis, at passage 3 (P3) after sorting, the c-kit-positive cells reached 93.4±0.95%, but were negative for the hematopoietic and endothelial antigens, CD45 (2.1±0.26%), CD31 (1.67±0.35%), CD34 (3.4±0.5%) and KDR (2.8±0.42%). As expected, they were positive for the control mesenchymal markerS, CD90 (71.6±1.55%), CD29 (93.7±1.2%), and THYE stemness marker Sca-1 (82.33±0.90%). (B) Immunofluorescence staining of the main cardiac lineages differentiated from c-kit + cells, namely (panel b) the cardiomyocyte marker, TnI; (panel c) the smooth muscle cell marker, SMA; and (panel d) the endothelial cell marker, vWF. The expression of the cardiac lineage markers (panel e) GATA-4; and (panel f) Nkx2.5 in the c-kit + cells was also analyzed. Nuclei were counterstained with DAPI.

    Journal: International Journal of Molecular Medicine

    Article Title: Macrophage migration inhibitory factor promotes cardiac stem cell proliferation and endothelial differentiation through the activation of the PI3K/Akt/mTOR and AMPK pathways

    doi: 10.3892/ijmm.2016.2542

    Figure Lengend Snippet: Identification of isolated cells. (A) As shown by flow cytometry analysis, at passage 3 (P3) after sorting, the c-kit-positive cells reached 93.4±0.95%, but were negative for the hematopoietic and endothelial antigens, CD45 (2.1±0.26%), CD31 (1.67±0.35%), CD34 (3.4±0.5%) and KDR (2.8±0.42%). As expected, they were positive for the control mesenchymal markerS, CD90 (71.6±1.55%), CD29 (93.7±1.2%), and THYE stemness marker Sca-1 (82.33±0.90%). (B) Immunofluorescence staining of the main cardiac lineages differentiated from c-kit + cells, namely (panel b) the cardiomyocyte marker, TnI; (panel c) the smooth muscle cell marker, SMA; and (panel d) the endothelial cell marker, vWF. The expression of the cardiac lineage markers (panel e) GATA-4; and (panel f) Nkx2.5 in the c-kit + cells was also analyzed. Nuclei were counterstained with DAPI.

    Article Snippet: To identify the differentiation of CSCs into myocardial cells or smooth muscle cells, mouse anti-TnI (1:100; ab19615; Abcam, Cambridge, MA, USA) and mouse anti-SMA (1:100, BM0002; Boster, Wuhan, China) were used.

    Techniques: Isolation, Flow Cytometry, Cytometry, Marker, Immunofluorescence, Staining, Expressing