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Anti pegfr

Manufactured by Merck Group
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Sourced in United Kingdom

Anti-pEGFR is a laboratory product used for the detection and quantification of phosphorylated epidermal growth factor receptor (pEGFR) in various biological samples. It is designed to provide a reliable and accurate method for researchers to analyze the activation status of EGFR, which is a key signaling protein involved in cell growth and proliferation.

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Lab products found in correlation

Anti akt, by Cell Signaling Technology (2 mentions) Anti p akt, by Cell Signaling Technology (2 mentions) Sorafenib, by LGC (1 mentions) Osimertinib, by Selleck Chemicals (1 mentions) Lapatinib, by Selleck Chemicals (1 mentions) Anti igf1rβ, by Cell Signaling Technology (1 mentions) Anti p c met, by Cell Signaling Technology (1 mentions) Anti src, by Cell Signaling Technology (1 mentions) Anti lck, by Cell Signaling Technology (1 mentions) Anti p stat3, by Cell Signaling Technology (1 mentions) Anti fgfr1, by Cell Signaling Technology (1 mentions) Sb203580, by Cayman Chemical (1 mentions) Bibf1120, by Selleck Chemicals (1 mentions) Anti lyn, by Cell Signaling Technology (1 mentions) Anti pten, by Cell Signaling Technology (1 mentions) Anti stat3, by Cell Signaling Technology (1 mentions) Anti pigf1r β, by Cell Signaling Technology (1 mentions) Anti fyn, by Cell Signaling Technology (1 mentions) Anti yes, by Cell Signaling Technology (1 mentions) Anti pfgfr, by Cell Signaling Technology (1 mentions)

2 protocols using anti pegfr

1

Anticancer Compounds Characterization

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Erlotinib was kindly provided by F. Hoffman-La Roche Ltd, gefitinib was provided by AstraZeneca Inc; VS-4718 was provided by Verastem Inc; afatinib, osimertinib, lapatinib, AZD4547, and BIBF1120 were purchased from Selleck Chemicals; SU11274 and picropodophyllin were from Carbiochem; dasatinib was from Bio Vision; SB203580 was from Cayman Chemical; sorafenib was acquired from Toronto Research Chemicals Inc, cisplatin was from Bristol-Myers Squibb Company; and PD173074 was from Sigma-Aldrich.
Anti-HER2 and anti-pHER2 antibodies were purchased from Merck Millipore Corporation, anti-EGFR, anti-pEGFR, anti-pHER3, anti-HER4, anti-pHER4, anti-pc-Met, anti-IGF1Rβ, anti-pIGF1Rβ, anti-PDGFRβ, anti-pPDGFRβ, anti-FGFR1, anti-pFGFR, anti-ERK1/2, anti-pERK1/2, anti-AKT, anti-pAKT, anti-STAT3, anti-pSTAT3, anti-PTEN, anti-SRC, anti-FYN, anti-LYN, anti-YES, anti-LCK, anti-pSRC family (Y416), anti-pSRC (Y527), anti-FAK, anti-pFAK (Y397), anti-pFAK (Y576/577), anti-pFAK (Y925) and anti- EGFR (del E746-A750) antibody were from Cell Signaling Technology, anti-HER3 and anti-c-Met were from Santa Cruz Biotechnology Inc, anti-β-actin was from Abcam, Inc., and anti-α-tubulin was from Sigma-Aldrich.
Murakami Y., Sonoda K., Abe H., Watari K., Kusakabe D., Azuma K., Kawahara A., Akiba J., Oneyama C., Pachter J.A., Sakai K., Nishio K., Kuwano M, & Ono M. (2017). The activation of SRC family kinases and focal adhesion kinase with the loss of the amplified, mutated EGFR gene contributes to the resistance to afatinib, erlotinib and osimertinib in human lung cancer cells. Oncotarget, 8(41), 70736-70751.
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2

Western Blotting for Protein Analysis

Cited 1 time
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Western blotting assays were performed as previously described [16 (link)]. The following antibodies were used in the analysis: anti-ADAM15 (sc-365752), anti-CD151 (sc-271216) (Santa Cruz, CA, USA), anti-Integrin αV (ab179475), anti-Integrin α3 (ab242196), anti-Integrin α6 (ab20142), and anti-Integrin β1 (ab52971) antibodies (Abcam, London, UK), followed by the p-Her2 (Sigma-Aldrich; Merck KGaA, SAB4300061), anti-p-EGFR (#3777), anti-EGFR (#4267), anti-Her2 (#4290), anti-p-FAK (#8556), anti-FAK (#13009), anti-p-AKT (#4060), anti-AKT (#4691), anti-p-ERK (#4370), anti-ERK (#4695), anti-CyclinD1 (#2978), anti-MMP9 (#13667) (Cell Signaling Technology Danvers, MA, USA). Anti-β-actin (CW0096M) and anti-mouse (CW0102) or anti-rabbit (CW0103) secondary antibodies were purchased from Cowin (China).
Zhou J., Wang A., Cai T., Li Y., Du W., Zhang Y., Zhang R., Zhang W., Zhu J., Zeng Y., Huang J.A, & Liu Z. (2022). Integrin α3/α6 and αV are implicated in ADAM15-activated FAK and EGFR signalling pathway individually and promote non-small-cell lung cancer progression. Cell Death & Disease, 13(5), 486.
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