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phycoerythrin conjugated mouse monoclonal anti human c kit cd117  (R&D Systems)


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    R&D Systems phycoerythrin conjugated mouse monoclonal anti human c kit cd117
    Phycoerythrin Conjugated Mouse Monoclonal Anti Human C Kit Cd117, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+kit+cd117+monoclonal+antibody/Human+CD117%2Fc-kit+PE-conjugated+Antibody/pm35955836-391-12-17
    Average 92 stars, based on 6 article reviews
    phycoerythrin conjugated mouse monoclonal anti human c kit cd117 - by Bioz Stars, 2026-10
    92/100 stars

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    Related Articles

    Expressing:

    Article Title: Activity of triptolide against human mast cells harboring the kinase domain mutant KIT
    Article Snippet: Dexamethasone was from Guangzhou Baiyunshan Pharmaceutical Co (Guangzhou, China).. Antibodies and their sources were as follows: rabbit polyclonal antibodies against Bax, Mcl‐1 (S‐19), KIT (c‐19), phospho‐KIT on Y568/570, were from Santa Cruz Biotechnology (Santa Cruz, CA, US); antibodies against poly(adenosine diphosphate [ADP]‐ribose) polymerase (PARP), p27Kip1 and p53, Becton‐Dickson Biosciences Pharmingen (San Jose, CA, US); antibodies against phospho‐Erk1/2 (T202/Y204), Erk1/2, Akt, JNK, and XIAP were from Cell Signaling Technology (Beverly, MA, US); mouse monoclonal antibody specific against phosphotyrosine 705 of Stat3 (clone 9E12) and rabbit polyclonal anti‐Stat3, Upstate Technology (Lake Placid, NY, US); mouse anti‐human‐KIT (CD117) monoclonal antibody, R&D Systems (Minneapolis, MN, US); mouse monoclonal antibody against actin, Sigma‐Aldrich (Shanghai, China); rabbit anti‐human RNA polymerase II, phospho‐RNA polymerase II (S5), Bethyl Laboratories (Montgomery, TX, US); and anti‐mouse IgG and anti‐rabbit IgG horseradish peroxidase‐conjugated antibodies, Pierce Biotechnology (Rockford, IL, US).. Cell viability assay.

    Control:

    Article Title: Activity of triptolide against human mast cells harboring the kinase domain mutant KIT
    Article Snippet: Dexamethasone was from Guangzhou Baiyunshan Pharmaceutical Co (Guangzhou, China).. Antibodies and their sources were as follows: rabbit polyclonal antibodies against Bax, Mcl‐1 (S‐19), KIT (c‐19), phospho‐KIT on Y568/570, were from Santa Cruz Biotechnology (Santa Cruz, CA, US); antibodies against poly(adenosine diphosphate [ADP]‐ribose) polymerase (PARP), p27Kip1 and p53, Becton‐Dickson Biosciences Pharmingen (San Jose, CA, US); antibodies against phospho‐Erk1/2 (T202/Y204), Erk1/2, Akt, JNK, and XIAP were from Cell Signaling Technology (Beverly, MA, US); mouse monoclonal antibody specific against phosphotyrosine 705 of Stat3 (clone 9E12) and rabbit polyclonal anti‐Stat3, Upstate Technology (Lake Placid, NY, US); mouse anti‐human‐KIT (CD117) monoclonal antibody, R&D Systems (Minneapolis, MN, US); mouse monoclonal antibody against actin, Sigma‐Aldrich (Shanghai, China); rabbit anti‐human RNA polymerase II, phospho‐RNA polymerase II (S5), Bethyl Laboratories (Montgomery, TX, US); and anti‐mouse IgG and anti‐rabbit IgG horseradish peroxidase‐conjugated antibodies, Pierce Biotechnology (Rockford, IL, US).. Cell viability assay.



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    The anti-p17 mAb (6E3) specifically recognized CHO suspension cells transiently transfected with p17-expressing plasmid. ( A ) Identification of the mAb subtypes. ( B ) Identification of antibody titer of the purified 6E3 by the ELISA method. ( C ) 293T cells were transfected with pcDNA3.1- D117L -strep or control plasmid. Cells were fixed at 24 h post-transfection and immunostained with 6E3 as primary antibody and FITC-conjugated goat anti-mouse IgG as second antibody. Cellular nuclei were counterstained with 1 μg/mL of 4′,6′-diamidino-2-phenylindole (DAPI). ( D ) WB was conducted as treated in ( C ) to show the reactivity of 6E3.

    Journal: Viruses

    Article Title: The Indirect ELISA and Monoclonal Antibody against African Swine Fever Virus p17 Revealed Efficient Detection and Application Prospects

    doi: 10.3390/v15010050

    Figure Lengend Snippet: The anti-p17 mAb (6E3) specifically recognized CHO suspension cells transiently transfected with p17-expressing plasmid. ( A ) Identification of the mAb subtypes. ( B ) Identification of antibody titer of the purified 6E3 by the ELISA method. ( C ) 293T cells were transfected with pcDNA3.1- D117L -strep or control plasmid. Cells were fixed at 24 h post-transfection and immunostained with 6E3 as primary antibody and FITC-conjugated goat anti-mouse IgG as second antibody. Cellular nuclei were counterstained with 1 μg/mL of 4′,6′-diamidino-2-phenylindole (DAPI). ( D ) WB was conducted as treated in ( C ) to show the reactivity of 6E3.

    Article Snippet: The subtypes of 6E3 were identified using a monoclonal antibody isotype identification kit (Proteintech Group, Inc., Chicago, IL, USA) according to the manufacturer’s instructions.

    Techniques: Suspension, Transfection, Expressing, Plasmid Preparation, Purification, Enzyme-linked Immunosorbent Assay, Control