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rabbit anti ficolin a polyclonal antibody  (Proteintech)


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    Proteintech rabbit anti ficolin a polyclonal antibody
    Rabbit Anti Ficolin A Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+ficolin+a+polyclonal+antibody/FCN1+Antibody/pm36052069-94-36-46
    Average 93 stars, based on 7 article reviews
    rabbit anti ficolin a polyclonal antibody - by Bioz Stars, 2026-10
    93/100 stars

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    Immunodetection:

    Article Title: The complex formation of MASP-3 with pattern recognition molecules of the lectin complement pathway retains MASP-3 in the circulation.
    Article Snippet: .. The blotted membranes were separately subjected to immunodetection using following primary antibodies; HRP-conjugated rat antimouse MBL-A monoclonal antibody (clone: 8G6, Hycult Biotech, Plymouth Meeting, PA, USA), HRP-conjugated rat anti-mouse MBL-C monoclonal antibody (clone: 16A8, Hycult Biotech), rabbit anti-ficolin-A polyclonal antibody (25), and rabbit anti-CL-K1 polyclonal antibody (Proteintech, Rosemont, IL, USA), followed by reaction with a HRPconjugated secondary antibody for rabbit first antibodies. .. After the membranes were treated with ECL Prime Western Blotting Detection System, objective protein bands were visualized by chemiluminescence detection using the Amersham Imager 600.

    Article Title: The complex formation of MASP-3 with pattern recognition molecules of the lectin complement pathway retains MASP-3 in the circulation
    Article Snippet: .. The blotted membranes were separately subjected to immunodetection using following primary antibodies; HRP-conjugated rat anti-mouse MBL-A monoclonal antibody (clone: 8G6, Hycult Biotech, Plymouth Meeting, PA, USA), HRP-conjugated rat anti-mouse MBL-C monoclonal antibody (clone: 16A8, Hycult Biotech), rabbit anti-ficolin-A polyclonal antibody , and rabbit anti-CL-K1 polyclonal antibody (Proteintech, Rosemont, IL, USA), followed by reaction with a HRP-conjugated secondary antibody for rabbit first antibodies. .. After the membranes were treated with ECL Prime Western Blotting Detection System, objective protein bands were visualized by chemiluminescence detection using the Amersham Imager 600.



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    Image Search Results


    VWF is transported in circulating EVs from GBM patients. ( A ) Equal volume of protein lysates from EV fractions, obtained with SEC followed by ultracentrifugation, and their corresponding plasma, from one GBM patient and one healthy donor, were separated by SDS-PAGE and analyzed by immunoblot for VWF, FCN3, and HSP70. Blots are representative of n = 3. ( B ) mRNA expression of von Willebrand factor (VWF) and ficolin-3 (FCN3) in healthy subjects and GBM patients estimated from The Cancer Genome Atlas (TCGA, n > 500 for GBM patients). ( C ) Anomalies currently reported in VWF and FCN3 genes. ( D ) Equal volume of protein lysates from EV fractions (3 GBM and 3 Healthy) were separated by SDS-PAGE and analyzed by immunoblot for VWF, GM130 (putative intracellular membrane protein contaminant), and Apolipoprotein A1 (APOA1, plasmatic protein). Healthy donor plasma and total cell lysate from GBM cells serve as controls. Blots are representative of n > 7 individual samples. ( E ) Densitometric analysis was performed on 7 and 8 independent EV preparations from Healthy and GBM liquid biopsies, respectively. ( F ) Concentration of VWF in plasmatic EVs from healthy donors and GBM patients (n = 20). Mann–Whitney test, * p < 0.05, ** p < 0.01, *** p < 0.001. S.D. are shown in panel E and S.E.M. in panel F.

    Journal: Scientific Reports

    Article Title: The von Willebrand factor stamps plasmatic extracellular vesicles from glioblastoma patients

    doi: 10.1038/s41598-021-02254-7

    Figure Lengend Snippet: VWF is transported in circulating EVs from GBM patients. ( A ) Equal volume of protein lysates from EV fractions, obtained with SEC followed by ultracentrifugation, and their corresponding plasma, from one GBM patient and one healthy donor, were separated by SDS-PAGE and analyzed by immunoblot for VWF, FCN3, and HSP70. Blots are representative of n = 3. ( B ) mRNA expression of von Willebrand factor (VWF) and ficolin-3 (FCN3) in healthy subjects and GBM patients estimated from The Cancer Genome Atlas (TCGA, n > 500 for GBM patients). ( C ) Anomalies currently reported in VWF and FCN3 genes. ( D ) Equal volume of protein lysates from EV fractions (3 GBM and 3 Healthy) were separated by SDS-PAGE and analyzed by immunoblot for VWF, GM130 (putative intracellular membrane protein contaminant), and Apolipoprotein A1 (APOA1, plasmatic protein). Healthy donor plasma and total cell lysate from GBM cells serve as controls. Blots are representative of n > 7 individual samples. ( E ) Densitometric analysis was performed on 7 and 8 independent EV preparations from Healthy and GBM liquid biopsies, respectively. ( F ) Concentration of VWF in plasmatic EVs from healthy donors and GBM patients (n = 20). Mann–Whitney test, * p < 0.05, ** p < 0.01, *** p < 0.001. S.D. are shown in panel E and S.E.M. in panel F.

    Article Snippet: EVs were separated and concentrated from 500 μl of plasma as described above and the pellet was directly lysed in boiling Laemmli for 10 min. Proteins were resolved by SDS-PAGE, transferred onto nitrocellulose membranes and blotted with the following antibodies, all diluted at 1/1000: CD9 (EXOAB-CD9A-1, SBI), CD63 (EXOAB-CD63A-1, SBI), VWF (sc-53466, Santa Cruz), FCN3 (CL7767AP, Cedarlane) , Apolipoprotein A1 (sc-376818, Santa Cruz), HSP70 (EXOAB-HSP70A, SBI), and GM130 (ab52649, Abcam) diluted at 1/1000.

    Techniques: Clinical Proteomics, SDS Page, Western Blot, Expressing, Membrane, Concentration Assay, MANN-WHITNEY