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erbb2 py 1248  (R&D Systems)


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    Structured Review

    R&D Systems erbb2 py 1248
    Western blot analysis of <t>ErbB2</t> pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.
    Erbb2 Py 1248, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/erbb2 py 1248/product/R&D Systems
    Average 92 stars, based on 11 article reviews
    erbb2 py 1248 - by Bioz Stars, 2026-06
    92/100 stars

    Images

    1) Product Images from "ErbB2 pY ‐1248 as a predictive biomarker for Parkinson's disease based on research with RPPA technology and in vivo verification"

    Article Title: ErbB2 pY ‐1248 as a predictive biomarker for Parkinson's disease based on research with RPPA technology and in vivo verification

    Journal: CNS Neuroscience & Therapeutics

    doi: 10.1111/cns.14407

    Western blot analysis of ErbB2 pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.
    Figure Legend Snippet: Western blot analysis of ErbB2 pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.

    Techniques Used: Western Blot

    Western blot analysis of ErbB2 pY‐1248 in mouse PD model. (A) Representative images of western blot of ErbB2 pY‐1248 in the mouse brain tissues. (B) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 was normalized to β‐Actin. *** p < 0.001 vs. Ctl.
    Figure Legend Snippet: Western blot analysis of ErbB2 pY‐1248 in mouse PD model. (A) Representative images of western blot of ErbB2 pY‐1248 in the mouse brain tissues. (B) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 was normalized to β‐Actin. *** p < 0.001 vs. Ctl.

    Techniques Used: Western Blot



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    Western blot analysis of <t>ErbB2</t> pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.
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    Western blot analysis of <t>ErbB2</t> pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.
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    Image Search Results


    Western blot analysis of ErbB2 pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.

    Journal: CNS Neuroscience & Therapeutics

    Article Title: ErbB2 pY ‐1248 as a predictive biomarker for Parkinson's disease based on research with RPPA technology and in vivo verification

    doi: 10.1111/cns.14407

    Figure Lengend Snippet: Western blot analysis of ErbB2 pY‐1248 , ErbB2, and ErbB1 in cellular PD model. (A, C) Representative images of western blot of ErbB2 pY‐1248 , ErbB2, and ErbB1 in extracted protein lysates from SH‐SY5Y cells treated with 6‐OHDA for 6 h. (B, D) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 and ErbB1 were normalized to ErbB2 and β‐Actin, respectively. It is presented as mean ± SEM. *** p < 0.001 vs. Ctl.

    Article Snippet: After blocking with 5% skim milk in TBST for 2 h at room temperature, membranes were incubated overnight at 4°C with primary antibodies against β actin (1:5000, A5441, Sigma), ErbB2 pY‐1248 (1:1000, AF1768, R&D Systems), ErbB2 (1:400, sc‐377,344, Santa Cruz Biotechnology), and ErbB1 (1:400, 2232S, Cell Signaling Technology).

    Techniques: Western Blot

    Western blot analysis of ErbB2 pY‐1248 in mouse PD model. (A) Representative images of western blot of ErbB2 pY‐1248 in the mouse brain tissues. (B) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 was normalized to β‐Actin. *** p < 0.001 vs. Ctl.

    Journal: CNS Neuroscience & Therapeutics

    Article Title: ErbB2 pY ‐1248 as a predictive biomarker for Parkinson's disease based on research with RPPA technology and in vivo verification

    doi: 10.1111/cns.14407

    Figure Lengend Snippet: Western blot analysis of ErbB2 pY‐1248 in mouse PD model. (A) Representative images of western blot of ErbB2 pY‐1248 in the mouse brain tissues. (B) Grayscale value analysis of the immunoblots. The band intensity of ErbB2 pY‐1248 was normalized to β‐Actin. *** p < 0.001 vs. Ctl.

    Article Snippet: After blocking with 5% skim milk in TBST for 2 h at room temperature, membranes were incubated overnight at 4°C with primary antibodies against β actin (1:5000, A5441, Sigma), ErbB2 pY‐1248 (1:1000, AF1768, R&D Systems), ErbB2 (1:400, sc‐377,344, Santa Cruz Biotechnology), and ErbB1 (1:400, 2232S, Cell Signaling Technology).

    Techniques: Western Blot