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  • 90
    ATCC paraná none exophiala bergeri cbs 663 76 dh 16149 wood none
    Paraná None Exophiala Bergeri Cbs 663 76 Dh 16149 Wood None, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/paraná none exophiala bergeri cbs 663 76 dh 16149 wood none/product/ATCC
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    paraná none exophiala bergeri cbs 663 76 dh 16149 wood none - by Bioz Stars, 2024-04
    90/100 stars
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    93
    Proteintech rabbit cardiac troponin i
    Rabbit Cardiac Troponin I, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit cardiac troponin i/product/Proteintech
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit cardiac troponin i - by Bioz Stars, 2024-04
    93/100 stars
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    94
    Proteintech anti mouse troponin i tni antibodies
    Intravenously transplanted MSCs attenuated endoplasmic reticulum stress-induced apoptosis. A and B. Representative TEM images and long-axis length of dilated endoplasmic reticulum (ER) of ventricular tissue in mice administered with PBS (control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. The dilated ER was identified by a yellow arrow. Scale bar, 1 μm, ( n = 5). **** P < 0.0001 vs Control, #### P < 0.0001 vs Dox/PBS, &&&& P < 0.0001 vs Dox/Single dose. C. Representative immunofluorescence images of cardiac <t>troponin</t> <t>I</t> (cTnI, red) and GRP78 antibody (green) binding to ventricular tissue of mice administered with PBS (control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. Scale bar, 100 μm. D. Statistics of the fluorescence intensity of GRP78 in each group on day 14 ( n = 5). *** P < 0.001, **** P < 0.0001 vs Control, && P < 0.01 vs Dox/Single dose. E and F. Western Blotting and quantified protein expression of the ER stress-induced apoptosis pathway in ventricular tissue of mice administrated with PBS (Control), Dox/PBS, Dox/Single dose on days 7 and 14, ( n = 5). * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 vs Control, # P < 0.05, ## P < 0.01, ### P < 0.001, #### P < 0.0001 vs Dox/PBS, &&& P < 0.001, &&&& P < 0.0001 vs Dox/Single dose. G and H. TUNEL assay (green) and apoptotic proportion of ventricular tissue in mice administrated with PBS (Control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. Scale bar, 50 μm ( n = 5). **** P < 0.0001 vs Control, #### P < 0.0001 vs Dox/PBS, &&&& P < 0.0001 vs Dox/Single dose. Data were analyzed by one-way ANOVA followed by Bonferroni post hoc test, unless specifically indicated
    Anti Mouse Troponin I Tni Antibodies, supplied by Proteintech, 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/result/anti mouse troponin i tni antibodies/product/Proteintech
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti mouse troponin i tni antibodies - by Bioz Stars, 2024-04
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    94
    Proteintech ctni tnni3
    Validating the pH-sensitivity of troponin and Crip2 genes. A Western blot of whole-cell lysates collected from NRVMs after 48 h of culture in serum-free medium at one of four test pH levels for cardiac troponin-T (cTnT; Tnnt2 ), cardiac troponin-I (cTnI; <t>Tnni3</t> ) and slow skeletal troponin-I (ssTnI; Tnni1 ). β-actin was re-developed using the same membrane as that used for ssTnI. B ELISA absorbance for cTnT, cTnI and ssTnI, and β-actin as a function of pH, normalized to mean signal (average from 4 isolations). ** P < 0.01 and * P < 0.05 by ANOVA. C CRIP2 protein quantified by whole-cell ELISA, showing similar pH-dependence to transcript level (4 repeats). D Western blot of whole-cell lysates collected from NRVMs after 48 h of culture in serum-free medium at either pH 6.4 or 7.44. Each pair represents an independent isolation (i.e. biological repeat). Fractionated lysates showing pH-sensitivity of CRIP2 in the nucleus and cytoplasm, using lamin A/C and GAPDH as loading controls. E CRIP2 western blot of nuclear fractions of NRVM lysates confirm robust pH-responsiveness. F Immunofluorescence imaging of NRVM monolayers for CRIP2, G ssTnI (a pH-responsive DEG/DAP) and H G6PDH (a pH-insensitive protein). Red outlines indicate nuclear regions (Hoechst-33342). (I) Blot for NRVM lysates prepared after immunoprecipitation with CRIP2 antibody, following incubation at pH 6.4 or 7.4. IP blot compared to input. J Silver-stained gel produced from CRIP2 immunoprecipitation, highlighting gel areas selected for mass spectrometry. K Results of mass spectrometry analysis, highlighting proteins involved in contraction. Only proteins that were absent in the negative control (without CRIP2 antibody) but present in the IP are listed
    Ctni Tnni3, supplied by Proteintech, 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/result/ctni tnni3/product/Proteintech
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    94
    Proteintech antibody against cardiac troponin i
    The protein levels of NOX1 and NOX4 were increased by DOX both in vivo and in vitro . (A) Representative western blot analysis of NOX1 and NOX4 in myocardial tissue. (B,C) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 6 per group). (D,E) Representative images of NOX1 and NOX4 expression in myocardial tissue detected by the immunofluorescence. The nuclei were stained with DAPI (Scale bar = 50 µm). (F) Representative western blot analysis of NOX1 and NOX4 of NRCMs treated with DOX of different concentrations for 24 h (G,H) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 3). (I) Representative western blot analysis of NOX 1 and NOX 4 of NRCMs treated with DOX for different time. (J,K) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 4–5). * p < 0.05, ** p < 0.01, *** p < 0.001, n. s., not significant. NOX, NADPH oxidase; DOX, doxorubicin; cTnI, Cardiac troponin I.
    Antibody Against Cardiac Troponin I, supplied by Proteintech, 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/result/antibody against cardiac troponin i/product/Proteintech
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    antibody against cardiac troponin i - by Bioz Stars, 2024-04
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    Image Search Results


    Intravenously transplanted MSCs attenuated endoplasmic reticulum stress-induced apoptosis. A and B. Representative TEM images and long-axis length of dilated endoplasmic reticulum (ER) of ventricular tissue in mice administered with PBS (control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. The dilated ER was identified by a yellow arrow. Scale bar, 1 μm, ( n = 5). **** P < 0.0001 vs Control, #### P < 0.0001 vs Dox/PBS, &&&& P < 0.0001 vs Dox/Single dose. C. Representative immunofluorescence images of cardiac troponin I (cTnI, red) and GRP78 antibody (green) binding to ventricular tissue of mice administered with PBS (control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. Scale bar, 100 μm. D. Statistics of the fluorescence intensity of GRP78 in each group on day 14 ( n = 5). *** P < 0.001, **** P < 0.0001 vs Control, && P < 0.01 vs Dox/Single dose. E and F. Western Blotting and quantified protein expression of the ER stress-induced apoptosis pathway in ventricular tissue of mice administrated with PBS (Control), Dox/PBS, Dox/Single dose on days 7 and 14, ( n = 5). * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 vs Control, # P < 0.05, ## P < 0.01, ### P < 0.001, #### P < 0.0001 vs Dox/PBS, &&& P < 0.001, &&&& P < 0.0001 vs Dox/Single dose. G and H. TUNEL assay (green) and apoptotic proportion of ventricular tissue in mice administrated with PBS (Control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. Scale bar, 50 μm ( n = 5). **** P < 0.0001 vs Control, #### P < 0.0001 vs Dox/PBS, &&&& P < 0.0001 vs Dox/Single dose. Data were analyzed by one-way ANOVA followed by Bonferroni post hoc test, unless specifically indicated

    Journal: Stem Cell Research & Therapy

    Article Title: Intravenously transplanted mesenchymal stromal cells: a new endocrine reservoir for cardioprotection

    doi: 10.1186/s13287-022-02922-z

    Figure Lengend Snippet: Intravenously transplanted MSCs attenuated endoplasmic reticulum stress-induced apoptosis. A and B. Representative TEM images and long-axis length of dilated endoplasmic reticulum (ER) of ventricular tissue in mice administered with PBS (control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. The dilated ER was identified by a yellow arrow. Scale bar, 1 μm, ( n = 5). **** P < 0.0001 vs Control, #### P < 0.0001 vs Dox/PBS, &&&& P < 0.0001 vs Dox/Single dose. C. Representative immunofluorescence images of cardiac troponin I (cTnI, red) and GRP78 antibody (green) binding to ventricular tissue of mice administered with PBS (control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. Scale bar, 100 μm. D. Statistics of the fluorescence intensity of GRP78 in each group on day 14 ( n = 5). *** P < 0.001, **** P < 0.0001 vs Control, && P < 0.01 vs Dox/Single dose. E and F. Western Blotting and quantified protein expression of the ER stress-induced apoptosis pathway in ventricular tissue of mice administrated with PBS (Control), Dox/PBS, Dox/Single dose on days 7 and 14, ( n = 5). * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001 vs Control, # P < 0.05, ## P < 0.01, ### P < 0.001, #### P < 0.0001 vs Dox/PBS, &&& P < 0.001, &&&& P < 0.0001 vs Dox/Single dose. G and H. TUNEL assay (green) and apoptotic proportion of ventricular tissue in mice administrated with PBS (Control), Dox/PBS, Dox/Single dose, or Dox/Consecutive doses on day 14. Scale bar, 50 μm ( n = 5). **** P < 0.0001 vs Control, #### P < 0.0001 vs Dox/PBS, &&&& P < 0.0001 vs Dox/Single dose. Data were analyzed by one-way ANOVA followed by Bonferroni post hoc test, unless specifically indicated

    Article Snippet: Cellular samples were co-stained with anti-Rabbit GRP78 antibodies (11,587-1-AP, Proteintech) and anti-mouse Troponin I (TnI) antibodies (66,376-1-Ig, Proteintech) or anti-mouse alpha-actinin (Actinin, ab18061, Abcam).

    Techniques: Immunofluorescence, Binding Assay, Fluorescence, Western Blot, Expressing, TUNEL Assay

    Validating the pH-sensitivity of troponin and Crip2 genes. A Western blot of whole-cell lysates collected from NRVMs after 48 h of culture in serum-free medium at one of four test pH levels for cardiac troponin-T (cTnT; Tnnt2 ), cardiac troponin-I (cTnI; Tnni3 ) and slow skeletal troponin-I (ssTnI; Tnni1 ). β-actin was re-developed using the same membrane as that used for ssTnI. B ELISA absorbance for cTnT, cTnI and ssTnI, and β-actin as a function of pH, normalized to mean signal (average from 4 isolations). ** P < 0.01 and * P < 0.05 by ANOVA. C CRIP2 protein quantified by whole-cell ELISA, showing similar pH-dependence to transcript level (4 repeats). D Western blot of whole-cell lysates collected from NRVMs after 48 h of culture in serum-free medium at either pH 6.4 or 7.44. Each pair represents an independent isolation (i.e. biological repeat). Fractionated lysates showing pH-sensitivity of CRIP2 in the nucleus and cytoplasm, using lamin A/C and GAPDH as loading controls. E CRIP2 western blot of nuclear fractions of NRVM lysates confirm robust pH-responsiveness. F Immunofluorescence imaging of NRVM monolayers for CRIP2, G ssTnI (a pH-responsive DEG/DAP) and H G6PDH (a pH-insensitive protein). Red outlines indicate nuclear regions (Hoechst-33342). (I) Blot for NRVM lysates prepared after immunoprecipitation with CRIP2 antibody, following incubation at pH 6.4 or 7.4. IP blot compared to input. J Silver-stained gel produced from CRIP2 immunoprecipitation, highlighting gel areas selected for mass spectrometry. K Results of mass spectrometry analysis, highlighting proteins involved in contraction. Only proteins that were absent in the negative control (without CRIP2 antibody) but present in the IP are listed

    Journal: Basic Research in Cardiology

    Article Title: Alkaline nucleoplasm facilitates contractile gene expression in the mammalian heart

    doi: 10.1007/s00395-022-00924-9

    Figure Lengend Snippet: Validating the pH-sensitivity of troponin and Crip2 genes. A Western blot of whole-cell lysates collected from NRVMs after 48 h of culture in serum-free medium at one of four test pH levels for cardiac troponin-T (cTnT; Tnnt2 ), cardiac troponin-I (cTnI; Tnni3 ) and slow skeletal troponin-I (ssTnI; Tnni1 ). β-actin was re-developed using the same membrane as that used for ssTnI. B ELISA absorbance for cTnT, cTnI and ssTnI, and β-actin as a function of pH, normalized to mean signal (average from 4 isolations). ** P < 0.01 and * P < 0.05 by ANOVA. C CRIP2 protein quantified by whole-cell ELISA, showing similar pH-dependence to transcript level (4 repeats). D Western blot of whole-cell lysates collected from NRVMs after 48 h of culture in serum-free medium at either pH 6.4 or 7.44. Each pair represents an independent isolation (i.e. biological repeat). Fractionated lysates showing pH-sensitivity of CRIP2 in the nucleus and cytoplasm, using lamin A/C and GAPDH as loading controls. E CRIP2 western blot of nuclear fractions of NRVM lysates confirm robust pH-responsiveness. F Immunofluorescence imaging of NRVM monolayers for CRIP2, G ssTnI (a pH-responsive DEG/DAP) and H G6PDH (a pH-insensitive protein). Red outlines indicate nuclear regions (Hoechst-33342). (I) Blot for NRVM lysates prepared after immunoprecipitation with CRIP2 antibody, following incubation at pH 6.4 or 7.4. IP blot compared to input. J Silver-stained gel produced from CRIP2 immunoprecipitation, highlighting gel areas selected for mass spectrometry. K Results of mass spectrometry analysis, highlighting proteins involved in contraction. Only proteins that were absent in the negative control (without CRIP2 antibody) but present in the IP are listed

    Article Snippet: Primary rabbit antibodies used were against CRIP2 (Crip2, Proteintech or Novus), ssTnI (Tnni1) , cTnI (Tnni3) , cTnT (Tnnt2) , myosin-3 (Myh3) , myosin light chain kinase 3 (Proteintech), myosin-6 ( Myh6 ), myosin-7 ( Myh-7 ), myosin light chain 2 (Novus), mouse monoclonal antibodies against lamin A/C (LMNA/C, CST), vimentin (VIM, CST), α-actinin (ACTN2, Proteintech) and HRP-conjugated primary antibodies against GAPDH and β-actin (GAPDH and ACTB, Proteintech) in dilutions recommended by manufacturer.

    Techniques: Western Blot, Enzyme-linked Immunosorbent Assay, Isolation, Immunofluorescence, Imaging, Immunoprecipitation, Incubation, Staining, Produced, Mass Spectrometry, Negative Control

    The protein levels of NOX1 and NOX4 were increased by DOX both in vivo and in vitro . (A) Representative western blot analysis of NOX1 and NOX4 in myocardial tissue. (B,C) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 6 per group). (D,E) Representative images of NOX1 and NOX4 expression in myocardial tissue detected by the immunofluorescence. The nuclei were stained with DAPI (Scale bar = 50 µm). (F) Representative western blot analysis of NOX1 and NOX4 of NRCMs treated with DOX of different concentrations for 24 h (G,H) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 3). (I) Representative western blot analysis of NOX 1 and NOX 4 of NRCMs treated with DOX for different time. (J,K) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 4–5). * p < 0.05, ** p < 0.01, *** p < 0.001, n. s., not significant. NOX, NADPH oxidase; DOX, doxorubicin; cTnI, Cardiac troponin I.

    Journal: Frontiers in Pharmacology

    Article Title: Setanaxib (GKT137831) Ameliorates Doxorubicin-Induced Cardiotoxicity by Inhibiting the NOX1/NOX4/Reactive Oxygen Species/MAPK Pathway

    doi: 10.3389/fphar.2022.823975

    Figure Lengend Snippet: The protein levels of NOX1 and NOX4 were increased by DOX both in vivo and in vitro . (A) Representative western blot analysis of NOX1 and NOX4 in myocardial tissue. (B,C) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 6 per group). (D,E) Representative images of NOX1 and NOX4 expression in myocardial tissue detected by the immunofluorescence. The nuclei were stained with DAPI (Scale bar = 50 µm). (F) Representative western blot analysis of NOX1 and NOX4 of NRCMs treated with DOX of different concentrations for 24 h (G,H) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 3). (I) Representative western blot analysis of NOX 1 and NOX 4 of NRCMs treated with DOX for different time. (J,K) Quantification of NOX1 and NOX4 expression relative to the β-actin level ( n = 4–5). * p < 0.05, ** p < 0.01, *** p < 0.001, n. s., not significant. NOX, NADPH oxidase; DOX, doxorubicin; cTnI, Cardiac troponin I.

    Article Snippet: An antibody against cardiac troponin I (66376-1-Ig) was purchased from Proteintech (Wuhan, China).

    Techniques: In Vivo, In Vitro, Western Blot, Expressing, Immunofluorescence, Staining