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polyclonal rabbit anti human egfr igg  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology polyclonal rabbit anti human egfr igg
    ( a ) Western blot analysis of <t>EGFR,</t> Nectin-4, and TROP-2 expression in the BC cell lines RT4 and RT112 and in the antigen-negative control cell line CHO. ( b ) Cell binding of the antibodies and conjugates to the target cells as demonstrated by flow cytometry. Binding of the isotype control antibody is shown in gray.
    Polyclonal Rabbit Anti Human Egfr Igg, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 2218 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+antibody+to+egfr/EGFR/pmc12736122-157-9-15
    Average 96 stars, based on 2218 article reviews
    polyclonal rabbit anti human egfr igg - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Exploring EGFR, Nectin-4, and TROP-2 as Therapeutic Targets for Bladder Cancer Photoimmunotherapy"

    Article Title: Exploring EGFR, Nectin-4, and TROP-2 as Therapeutic Targets for Bladder Cancer Photoimmunotherapy

    Journal: Molecules

    doi: 10.3390/molecules30244802

    ( a ) Western blot analysis of EGFR, Nectin-4, and TROP-2 expression in the BC cell lines RT4 and RT112 and in the antigen-negative control cell line CHO. ( b ) Cell binding of the antibodies and conjugates to the target cells as demonstrated by flow cytometry. Binding of the isotype control antibody is shown in gray.
    Figure Legend Snippet: ( a ) Western blot analysis of EGFR, Nectin-4, and TROP-2 expression in the BC cell lines RT4 and RT112 and in the antigen-negative control cell line CHO. ( b ) Cell binding of the antibodies and conjugates to the target cells as demonstrated by flow cytometry. Binding of the isotype control antibody is shown in gray.

    Techniques Used: Western Blot, Expressing, Negative Control, Binding Assay, Flow Cytometry, Control

    Graphical abstract illustrating the future clinical application of PIT using WB692-CB2 conjugates for the treatment of NMIBC. Following intravesical application of the antibody–dye conjugates into the bladder, they can be activated by cystoscopic red light for the selective eradication of BC cells expressing EGFR, Nectin-4 and/or TROP-2. For personalized PIT, a pre-therapeutic determination of target antigen expression in biopsy samples may guide the selection of an optimal conjugate combination. Created in BioRender. Wolf, I (2025) https://BioRender.com/sx866ld .
    Figure Legend Snippet: Graphical abstract illustrating the future clinical application of PIT using WB692-CB2 conjugates for the treatment of NMIBC. Following intravesical application of the antibody–dye conjugates into the bladder, they can be activated by cystoscopic red light for the selective eradication of BC cells expressing EGFR, Nectin-4 and/or TROP-2. For personalized PIT, a pre-therapeutic determination of target antigen expression in biopsy samples may guide the selection of an optimal conjugate combination. Created in BioRender. Wolf, I (2025) https://BioRender.com/sx866ld .

    Techniques Used: Expressing, Selection

    Related Articles

    Incubation:

    Article Title: Improved Efficiency of Microsurgical Enucleated Tripronuclear Zygotes Development and Embryonic Stem Cell Derivation by Supplementing Epidermal Growth Factor, Brain-Derived Neurotrophic Factor, and Insulin-Like Growth Factor-1
    Article Snippet: .. Slides were incubated separately overnight with the following antibodies at 4°C: rabbit polyclonal antibody to EGFR (1:100, sc374607; Santa Cruz Biotechnology), rabbit polyclonal antibody to TrkB (1:100, ab51190; Abcam, Inc.), and rabbit polyclonal antibody to IGF-1R (1:100, ab90657; Abcam, Inc.). .. Slides were incubated with FITC-conjugated anti-rabbit or anti-mouse secondary antibodies (Jackson Labs) for 1 h at 37°C before washing again in PBS.

    Article Title: Molecular Imaging of N-linked Glycosylation Suggests Glycan Biosynthesis Is a Novel Target for Cancer Therapy
    Article Snippet: .. The primary antibody was a rabbit polyclonal antibody to EGFR (Santa Cruz) which was added to the tumor sections at a 1:70 dilution and incubated for 45 minutes at room temperature. ..

    Article Title: Molecular Imaging of N-linked Glycosylation Suggests Glycan Biosynthesis is a Novel Target for Cancer Therapy
    Article Snippet: .. The primary antibody was a rabbit polyclonal antibody to EGFR (Santa Cruz) which was added to the tumor sections at a 1:70 dilution, and incubated for 45 minutes at room temperature. ..

    other:

    Article Title: Enhancing Akt imaging through targeted reporter expression
    Article Snippet: Rabbit polyclonal antibodies to Akt, phospho-Akt (phosphorylated on Ser473) and phospho-EGFR (Y845) were purchased from Cell Signaling Technology, and rabbit polyclonal antibody to EGFR (SC-03) was purchased from Santa Cruz biotechnology.



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    ( a ) Western blot analysis of <t>EGFR,</t> Nectin-4, and TROP-2 expression in the BC cell lines RT4 and RT112 and in the antigen-negative control cell line CHO. ( b ) Cell binding of the antibodies and conjugates to the target cells as demonstrated by flow cytometry. Binding of the isotype control antibody is shown in gray.
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    Altered protein expression and <t>EGFR</t> signaling in Sorcin-deficient lung development A ) Confocal microscopy of 3-week-old lung tissue from WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ lung tissue shows reduced SP-B (red) expression compared to WT. Scale bars, 20 μm B ) Western blot analysis of lung lysates from 3-week-old WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ mice exhibit decreased EGFR, PANRAS and RAB5C protein levels compared to WT. Densitometry quantification is shown (mean ± SEM). ** p < 0.01 (Student’s t-test), *** p < 0.001 (determined by Student’s t-test) C-E ) Confocal microscopy of 3-week-old lung sections: WT mice show epithelial localization of EGFR (green) (C), RAB5C (green) (D) and PANRAS (red) protein (E). In Sri⁻ / ⁻ mice, these proteins are significantly reduced. Scale bars, 20 μm
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    Santa Cruz Biotechnology anti egfr santa cruz sc101 rabbit polyclonal anti erk2
    Altered protein expression and <t>EGFR</t> signaling in Sorcin-deficient lung development A ) Confocal microscopy of 3-week-old lung tissue from WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ lung tissue shows reduced SP-B (red) expression compared to WT. Scale bars, 20 μm B ) Western blot analysis of lung lysates from 3-week-old WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ mice exhibit decreased EGFR, PANRAS and RAB5C protein levels compared to WT. Densitometry quantification is shown (mean ± SEM). ** p < 0.01 (Student’s t-test), *** p < 0.001 (determined by Student’s t-test) C-E ) Confocal microscopy of 3-week-old lung sections: WT mice show epithelial localization of EGFR (green) (C), RAB5C (green) (D) and PANRAS (red) protein (E). In Sri⁻ / ⁻ mice, these proteins are significantly reduced. Scale bars, 20 μm
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    Image Search Results


    ( a ) Western blot analysis of EGFR, Nectin-4, and TROP-2 expression in the BC cell lines RT4 and RT112 and in the antigen-negative control cell line CHO. ( b ) Cell binding of the antibodies and conjugates to the target cells as demonstrated by flow cytometry. Binding of the isotype control antibody is shown in gray.

    Journal: Molecules

    Article Title: Exploring EGFR, Nectin-4, and TROP-2 as Therapeutic Targets for Bladder Cancer Photoimmunotherapy

    doi: 10.3390/molecules30244802

    Figure Lengend Snippet: ( a ) Western blot analysis of EGFR, Nectin-4, and TROP-2 expression in the BC cell lines RT4 and RT112 and in the antigen-negative control cell line CHO. ( b ) Cell binding of the antibodies and conjugates to the target cells as demonstrated by flow cytometry. Binding of the isotype control antibody is shown in gray.

    Article Snippet: Following transfer, EGFR, Nectin-4 and TROP-2 were detected using polyclonal rabbit anti-human EGFR IgG (#sc-03-G, Santa Cruz Biotechnology, Dallas, TX, USA), polyclonal rabbit anti-human Nectin-4 IgG (#17402S, Cell Signaling Technologies, Danvers, MA, USA), and monoclonal rabbit anti-human TROP-2 IgG (#90540, Cell Signaling Technologies).

    Techniques: Western Blot, Expressing, Negative Control, Binding Assay, Flow Cytometry, Control

    Graphical abstract illustrating the future clinical application of PIT using WB692-CB2 conjugates for the treatment of NMIBC. Following intravesical application of the antibody–dye conjugates into the bladder, they can be activated by cystoscopic red light for the selective eradication of BC cells expressing EGFR, Nectin-4 and/or TROP-2. For personalized PIT, a pre-therapeutic determination of target antigen expression in biopsy samples may guide the selection of an optimal conjugate combination. Created in BioRender. Wolf, I (2025) https://BioRender.com/sx866ld .

    Journal: Molecules

    Article Title: Exploring EGFR, Nectin-4, and TROP-2 as Therapeutic Targets for Bladder Cancer Photoimmunotherapy

    doi: 10.3390/molecules30244802

    Figure Lengend Snippet: Graphical abstract illustrating the future clinical application of PIT using WB692-CB2 conjugates for the treatment of NMIBC. Following intravesical application of the antibody–dye conjugates into the bladder, they can be activated by cystoscopic red light for the selective eradication of BC cells expressing EGFR, Nectin-4 and/or TROP-2. For personalized PIT, a pre-therapeutic determination of target antigen expression in biopsy samples may guide the selection of an optimal conjugate combination. Created in BioRender. Wolf, I (2025) https://BioRender.com/sx866ld .

    Article Snippet: Following transfer, EGFR, Nectin-4 and TROP-2 were detected using polyclonal rabbit anti-human EGFR IgG (#sc-03-G, Santa Cruz Biotechnology, Dallas, TX, USA), polyclonal rabbit anti-human Nectin-4 IgG (#17402S, Cell Signaling Technologies, Danvers, MA, USA), and monoclonal rabbit anti-human TROP-2 IgG (#90540, Cell Signaling Technologies).

    Techniques: Expressing, Selection

    Altered protein expression and EGFR signaling in Sorcin-deficient lung development A ) Confocal microscopy of 3-week-old lung tissue from WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ lung tissue shows reduced SP-B (red) expression compared to WT. Scale bars, 20 μm B ) Western blot analysis of lung lysates from 3-week-old WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ mice exhibit decreased EGFR, PANRAS and RAB5C protein levels compared to WT. Densitometry quantification is shown (mean ± SEM). ** p < 0.01 (Student’s t-test), *** p < 0.001 (determined by Student’s t-test) C-E ) Confocal microscopy of 3-week-old lung sections: WT mice show epithelial localization of EGFR (green) (C), RAB5C (green) (D) and PANRAS (red) protein (E). In Sri⁻ / ⁻ mice, these proteins are significantly reduced. Scale bars, 20 μm

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Sorcin regulates alveolarization and airway tissue remodeling during lung morphogenesis

    doi: 10.1007/s00018-025-05870-y

    Figure Lengend Snippet: Altered protein expression and EGFR signaling in Sorcin-deficient lung development A ) Confocal microscopy of 3-week-old lung tissue from WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ lung tissue shows reduced SP-B (red) expression compared to WT. Scale bars, 20 μm B ) Western blot analysis of lung lysates from 3-week-old WT and Sri⁻ / ⁻ mice. Sri⁻ / ⁻ mice exhibit decreased EGFR, PANRAS and RAB5C protein levels compared to WT. Densitometry quantification is shown (mean ± SEM). ** p < 0.01 (Student’s t-test), *** p < 0.001 (determined by Student’s t-test) C-E ) Confocal microscopy of 3-week-old lung sections: WT mice show epithelial localization of EGFR (green) (C), RAB5C (green) (D) and PANRAS (red) protein (E). In Sri⁻ / ⁻ mice, these proteins are significantly reduced. Scale bars, 20 μm

    Article Snippet: Then, sections were blocked in 5% goat serum for 1 h and incubated overnight at 4 °C with primary antibody rabbit polyclonal EPCAM/CD326 (1:100 in 1%BSA-PBS solution) (Proteintech, #21050-1-AP), rabbit polyclonal SFTPB (1:100 in 1%BSA-PBS solution) (Thermo Fisher Scientific, # PA542000 ), rabbit polyclonal E-cadherin (1:100 in 1%BSA-PBS solution) (Proteintech, #20874-1-AP), mouse monoclonal E-cadherin (1:100 in 1%BSA-PBS solution) (BD Bioscience, #610181), mouse monoclonal α-Smooth Muscle Actin (1:100 in 1%BSA-PBS solution) (Sigma-Aldrich, #A5228), rabbit polyclonal EGFR (1:100 in 1%BSA-PBS solution) (Proteintech, #30847-1-AP) rabbit polyclonal RAB5C (1:100 in 1%BSA-PBS solution) (Thermo Fisher Scientific, #PA5101828), mouse monoclonal PANRAS (Ab3) (1:100 in 1%BSA-PBS solution) (Sigma-Aldrich, #OP40) followed by incubation with Alexa fluor 488 (rabbit)-conjugated secondary antibodies (1:500 in 1%BSA-PBS solution) (Thermo Fisher Scientific).

    Techniques: Expressing, Confocal Microscopy, Western Blot