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Horseradish peroxidase conjugated anti rabbit immunoglobulin g

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Horseradish peroxidase-conjugated anti-rabbit immunoglobulin G is a secondary antibody that binds to rabbit primary antibodies. The horseradish peroxidase enzyme conjugated to the antibody can be used to detect and visualize the presence of the bound primary antibody.

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Lab products found in correlation

Horseradish peroxidase conjugated anti mouse immunoglobulin g, by GeneTex (2 mentions) P egfr, by Cell Signaling Technology (2 mentions) Erk1 2, by Cell Signaling Technology (2 mentions) P erk1 2 t202 y204, by Cell Signaling Technology (1 mentions) Synaptophysin, by Cell Signaling Technology (1 mentions) P mek1 2, by Cell Signaling Technology (1 mentions) P erk1 2, by Cell Signaling Technology (1 mentions) Neurod1, by Abcam (1 mentions) Snail, by Abcam (1 mentions) Twist, by Abcam (1 mentions) Mek1 2, by Cell Signaling Technology (1 mentions) P akt, by Cell Signaling Technology (1 mentions) Vimentin, by GeneTex (1 mentions)

Close spelling variants of this product

Horseradish peroxidase (

2 protocols using horseradish peroxidase conjugated anti rabbit immunoglobulin g

1

Western Blotting of Signaling Proteins

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Western blotting was performed as previously described. The primary antibodies used included p-EGFR (T1068), EGFR, p-AKT (S473), AKT, p-MEK1/2 (S217/ 221), MEK1/2, p-ERK1/2 (T202/Y204), and ERK1/2, all from Cell Signaling Technology (Danvers, MA), BRAF (Abcam [Cambridge, MA]), and a-tubulin (Genetex, Zeeland, MI). Secondary antibodies used included horseradish peroxidase-conjugated anti-mouse immunoglobulin G and horseradish peroxidase-conjugated anti-rabbit immunoglobulin G (Genetex).
Ho C.C., Liao W.Y., Lin C.A., Shih J.Y., Yu C.J, & Yang J.C. (2017). Acquired BRAF V600E Mutation as Resistant Mechanism after Treatment with Osimertinib. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 12(3).
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2

Western Blotting Protein Analysis

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Western blotting was performed as previously described. The primary antibodies used included Rb, Synaptophysin, p-EGFR (T1068), EGFR, p-AKT (S473), AKT, p-MEK1/2 (S217/ 221), MEK1/2, p-ERK1/2 (T202/Y204), ERK1/2 (Cell Signaling Technology, Danvers, Massachusetts), NeuroD1, Zeb1, Twist, Snail, Slug (Abcam, Cambridge, United Kingdom) and CD44, Vimentin, GADH, and a-tubulin (Genetex, Zeeland, Michigan). Secondary antibodies used included horseradish peroxidase-conjugated anti-mouse immunoglobulin G and horseradish peroxidase-conjugated anti-rabbit immunoglobulin G (Genetex) antibodies.
Lin C.A., Yu S.L., Chen H.Y., Chen H.W., Lin S.U., Chang C.C., Yu C.J., Yang P.C, & Ho C.C. (2019). EGFR-Mutant SCLC Exhibits Heterogeneous Phenotypes and Resistance to Common Antineoplastic Drugs. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 14(3).
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