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image lab analyzer software  (Bio-Rad)


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    Bio-Rad image lab analyzer software
    Image Lab Analyzer Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 35737 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/image+lab+analyzer+software/Image+Lab+Software/pmc13013858-129-8-12
    Average 99 stars, based on 35737 article reviews
    image lab analyzer software - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Software:

    Article Title: NINJ1 plays a vital role in the release of neutrophil extracellular traps in acute lung injury
    Article Snippet: .. Band intensities were quantified using Image Lab Analyzer software (Bio-Rad, Hercules, 167 CA, USA). ..

    Article Title: MEOX1 triggers myofibroblast apoptosis resistance, contributing to pulmonary fibrosis in mice.
    Article Snippet: Funding information National Natural Science Foundation of China, Grant/Award Numbers: 82100084, 82170096; Natural Science Foundation of Hunan province, Grant/Award Number: 2023JJ30740; Natural Science Foundation of Changsha, Grant/Award Number: kq2208292 Abstract The apoptosis resistance of myofibroblasts is a hallmark in the irreversible progression of pulmonary fibrosis (PF).. While the underlying molecular mechanism remains elusive.. In this study, we unveiled a previously unrecognized mechanism underlying myofibroblast apoptosis resistance during PF.

    Article Title: Blocking triggering receptors expressed on myeloid cell-1 alleviates alveolar epithelial cell senescence by inhibiting oxidative stress in pulmonary fibrosis.
    Article Snippet: Pulmonary fibrosis (PF) is an insidious, progressive, and fatal age-associated disease that occurs primarily in older adults and has a poor prognosis.. Alveolar epithelial cell (AEC) senescence is the critical pathological mechanism of PF.. The accumulation of oxygen radicals, commonly referred to as reactive oxygen species (ROS), strongly contributes to cellular senescence.

    Article Title: Fibroblast growth factor-inducible 14 accelerates pulmonary fibrosis by inducing fibroblast senescence in mice
    Article Snippet: .. The relative band intensity was measured using the Image Lab Analyzer software (Bio-Rad, Hercules, CA, USA). ..

    Article Title: Blockade of TREM-1 alleviates alveolar epithelial cell senescence through Nrf2-mediated antioxidant pathways in pulmonary fibrosis
    Article Snippet: .. Protein signals were visualized using ChemiDoc XRS (Bio-Rad, USA) and the relative band intensity was quanti ed using Image Lab Analyzer software (Bio-Rad). .. Table 1 Antibody sources and dilutions antibody source catalog Dilution ratio Anti-p16 polyclonal antibody Abcam ab211542 1:2000 Anti-p21 polyclonal antibody Servicebio GB11153 1:2000 Anti-p53 polyclonal antibody Proteintech 10442-1-AP 1:2000 Anti-γ-H2AX polyclonal antibody Boster BM4841 1:2000 Anti-Nrf2 polyclonal antibody CST 12,721 1:2000 Anti-HO-1 polyclonal antibody Abcam ab52947 1:1500 Anti-TREM-1 monoclonal antibody Abcam AF1187 1:200 Anti-SPC polyclonal antibody Proteintech 10205-2-AP 1:200 Anti-α-tubulin monoclonal antibody Servicebio GB11200 1:10000 Statistical analyses In our study, all experiments were repeated at least three times independently.

    Article Title: The SARS-CoV-2 nucleocapsid protein induces microglia senescence-mediated cognitive impairment via Glycolysis
    Article Snippet: The membranes were incubated with the ECL reagent, and the chemiluminescent signals were captured using the ChemiDoc XRS imaging system (Bio-Rad, USA). .. The resulting images were analyzed using Image Lab Analyzer software (Bio-Rad), which allowed for precise quantification of protein band intensities. ..

    Western Blot:

    Article Title: MEOX1 triggers myofibroblast apoptosis resistance, contributing to pulmonary fibrosis in mice.
    Article Snippet: Funding information National Natural Science Foundation of China, Grant/Award Numbers: 82100084, 82170096; Natural Science Foundation of Hunan province, Grant/Award Number: 2023JJ30740; Natural Science Foundation of Changsha, Grant/Award Number: kq2208292 Abstract The apoptosis resistance of myofibroblasts is a hallmark in the irreversible progression of pulmonary fibrosis (PF).. While the underlying molecular mechanism remains elusive.. In this study, we unveiled a previously unrecognized mechanism underlying myofibroblast apoptosis resistance during PF.

    other:

    Article Title: Fibroblast growth factor-inducible 14 accelerates pulmonary fibrosis by inducing fibroblast senescence in mice.
    Article Snippet: After electrophoresis, samples were transferred to polyvinylidene fluoride membranes (Millipore, USA).

    Expressing:

    Article Title: IGF2BP3 participates in the pathogenesis of recurrent spontaneous abortion by regulating ferroptosis.
    Article Snippet: The aberrant invasive capability of trophoblast cells is widely acknowledged as a primary mechanism underlying RSA.. Recently, IGF2BP3 has been implicated in various cancers due to its influence on cellular invasion and migration.. However, whether IGF2BP3 involve in the occurrence of RSA and the specific functions it assumes in the development of RSA remain elusive.

    Incubation:

    Article Title: IGF2BP3 participates in the pathogenesis of recurrent spontaneous abortion by regulating ferroptosis.
    Article Snippet: The aberrant invasive capability of trophoblast cells is widely acknowledged as a primary mechanism underlying RSA.. Recently, IGF2BP3 has been implicated in various cancers due to its influence on cellular invasion and migration.. However, whether IGF2BP3 involve in the occurrence of RSA and the specific functions it assumes in the development of RSA remain elusive.



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    Spatial distribution and expression of cumulus cell genes linked to oocyte maturity. Validation of drivers through immunoblotting and immunofluorescence (A, B) analyses. HAS2 was shown for Network 1(MII Endpoint - GV Startpoint ); CASP3 for Network 2(GV Endpoint -GV Startpoint ); SEMA3A for Pairwise 3 (MII Endpoint - GV Endpoint . (A) Immunoblotting of the selected drivers. Blot quantification was made with <t>ImageLab</t> software by Bio-Rad. Data (mean ± SD) represent 3 independent sets of experiments (n = at least 3 biological replicates in each group per set; each biological replicate assayed in at least 3 technical replicates). * and *** Statistically significant values between the different studied groups (p<0.05 and p<0.001respectively). (B) Representative confocal images of co-immunofluorescence staining of nuclei (Hoechst), Alexa-Fluor 488 ( SEMA3A or CASP3 ) or Alexa-Fluor 568 ( HAS2 ) in CCs enclosing oocytes in the different nuclear stage. HAS2 and SEMA3A reactions for the MII Endpoint group were carried out on serial sections immediately adjacent to the equatorial plane of the same EAf. The equatorial section itself was used to document the oocyte nuclear stage (see <xref ref-type= Supplementary Datasheet 10 ). Likewise, CASP3 and SEMA3A reactions for the GV Endpoint group were performed on sections contiguous to the equatorial plane of the same EAf. Scale bar: 25 µm. " width="250" height="auto" />
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    Image Search Results


    Spatial distribution and expression of cumulus cell genes linked to oocyte maturity. Validation of drivers through immunoblotting and immunofluorescence (A, B) analyses. HAS2 was shown for Network 1(MII Endpoint - GV Startpoint ); CASP3 for Network 2(GV Endpoint -GV Startpoint ); SEMA3A for Pairwise 3 (MII Endpoint - GV Endpoint . (A) Immunoblotting of the selected drivers. Blot quantification was made with ImageLab software by Bio-Rad. Data (mean ± SD) represent 3 independent sets of experiments (n = at least 3 biological replicates in each group per set; each biological replicate assayed in at least 3 technical replicates). * and *** Statistically significant values between the different studied groups (p<0.05 and p<0.001respectively). (B) Representative confocal images of co-immunofluorescence staining of nuclei (Hoechst), Alexa-Fluor 488 ( SEMA3A or CASP3 ) or Alexa-Fluor 568 ( HAS2 ) in CCs enclosing oocytes in the different nuclear stage. HAS2 and SEMA3A reactions for the MII Endpoint group were carried out on serial sections immediately adjacent to the equatorial plane of the same EAf. The equatorial section itself was used to document the oocyte nuclear stage (see <xref ref-type= Supplementary Datasheet 10 ). Likewise, CASP3 and SEMA3A reactions for the GV Endpoint group were performed on sections contiguous to the equatorial plane of the same EAf. Scale bar: 25 µm. " width="100%" height="100%">

    Journal: Frontiers in Endocrinology

    Article Title: Tailor-made 3D in vitro maturation of early antral follicles uncovers cumulus-cell transcriptomic driver signature to predict oocyte competence

    doi: 10.3389/fendo.2025.1629815

    Figure Lengend Snippet: Spatial distribution and expression of cumulus cell genes linked to oocyte maturity. Validation of drivers through immunoblotting and immunofluorescence (A, B) analyses. HAS2 was shown for Network 1(MII Endpoint - GV Startpoint ); CASP3 for Network 2(GV Endpoint -GV Startpoint ); SEMA3A for Pairwise 3 (MII Endpoint - GV Endpoint . (A) Immunoblotting of the selected drivers. Blot quantification was made with ImageLab software by Bio-Rad. Data (mean ± SD) represent 3 independent sets of experiments (n = at least 3 biological replicates in each group per set; each biological replicate assayed in at least 3 technical replicates). * and *** Statistically significant values between the different studied groups (p<0.05 and p<0.001respectively). (B) Representative confocal images of co-immunofluorescence staining of nuclei (Hoechst), Alexa-Fluor 488 ( SEMA3A or CASP3 ) or Alexa-Fluor 568 ( HAS2 ) in CCs enclosing oocytes in the different nuclear stage. HAS2 and SEMA3A reactions for the MII Endpoint group were carried out on serial sections immediately adjacent to the equatorial plane of the same EAf. The equatorial section itself was used to document the oocyte nuclear stage (see Supplementary Datasheet 10 ). Likewise, CASP3 and SEMA3A reactions for the GV Endpoint group were performed on sections contiguous to the equatorial plane of the same EAf. Scale bar: 25 µm.

    Article Snippet: Densitometric analysis for protein quantification was conducted using ImageLab software analyzer (ImageLab v. 6.1.0 Bio-Rad Laboratories, Milan, Italy).

    Techniques: Expressing, Biomarker Discovery, Western Blot, Immunofluorescence, Software, Staining