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Horseradish peroxidase conjugated anti rabbit igg h l

Manufactured by Abcam
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Horseradish peroxidase-conjugated anti-rabbit IgG H&L is a secondary antibody that binds to the heavy and light chains of rabbit immunoglobulin G (IgG). The horseradish peroxidase (HRP) enzyme is covalently attached to the antibody, allowing for the detection of target proteins in applications such as Western blotting, ELISA, and immunohistochemistry.

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Lab products found in correlation

Anti fis1, by Abcam (1 mentions) Anti vdac, by Cell Signaling Technology (1 mentions) Anti drp1, by Cell Signaling Technology (1 mentions) Anti mfn2, by Cell Signaling Technology (1 mentions) Anti mfn1, by Cell Signaling Technology (1 mentions) Anti opa1, by Cell Signaling Technology (1 mentions) Anti h2ax ps139, by Cell Signaling Technology (1 mentions) Anti β tubulin, by Cell Signaling Technology (1 mentions) Anti c fos, by Cell Signaling Technology (1 mentions) Sch772984, by Targetmol (1 mentions) A438079, by Abcam (1 mentions) Anti gapdh, by Merck Group (1 mentions) Anti erk1 2, by Cell Signaling Technology (1 mentions) Anti β actin, by Merck Group (1 mentions) Dimethyl sulfoxide (dmso), by Merck Group (1 mentions) Anti ha, by BioLegend (1 mentions)

Close spelling variants of this product

Horseradish peroxidase-conjugated goat anti-rabbit IgG H&L Horseradish peroxidase-conjugated goat anti-rabbit IgG H&L (ab6721 Horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG H&L Horseradish peroxidase-conjugated secondary antibody of goat anti-rabbit IgG H&L Horseradish-peroxidase-conjugated goat anti-rabbit IgG H&L secondary antibody Horseradish peroxidase Rabbit anti-IgG IgG rabbit Rabbit anti-

2 protocols using horseradish peroxidase conjugated anti rabbit igg h l

1

Mitochondrial Dynamics and DNA Damage Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following primary antibodies were used for western blotting: anti-MFN1 (1:1000, Cell Signaling Technology, 14739S), anti-MFN2 (1:1000, Cell Signaling Technology, 9482S), anti-OPA1 (1:1000, Cell Signaling Technology, 80471S), anti-DRP1 (1:1000, Cell Signaling Technology, 8570S), anti-DRP1 p-S616 (1:1000, Cell Signaling Technology, 3455S), anti-FIS1 (1:1000, Abcam, ab156865), anti-H2A.X p-S139 (1:1000, Cell Signaling Technology 2577S), anti-VDAC (1:1000, Cell Signaling Technology, 4661S), anti-β-tubulin (1:1000, Cell Signaling Technology, 2146S) and horseradish peroxidase-conjugated anti-rabbit IgG H&L (1:10,000, Abcam, ab205718).
Baek M.L., Lee J., Pendleton K.E., Berner M.J., Goff E.B., Tan L., Martinez S.A., Mahmud I., Wang T., Meyer M.D., Lim B., Barrish J.P., Porter W., Lorenzi P.L, & Echeverria G.V. (2023). Mitochondrial structure and function adaptation in residual triple negative breast cancer cells surviving chemotherapy treatment. Oncogene, 42(14), 1117-1131.
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2

Antibody and Inhibitor Usage in Cell Signaling

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The antibodies used in this study were as follows: anti-phospho-c-Fos (pSer374) (Santa Cruz Biotechnology), anti-c-Fos (Cell Signaling Technology), anti-phospho-ERK1/2 (pThr202/pTyr204; Cell Signaling Technology), anti-ERK1/2 (Cell Signaling Technology), anti-HA (Biolegend), anti-GAPDH (Millipore), anti-β-actin (Millipore), horseradish peroxidase–conjugated anti-rabbit IgG H&L (Abcam), and horseradish peroxidase–conjugated anti-mouse IgG H&L (Abcam). ERK1/2 inhibitor (SCH772984">SCH772984; TargetMol) and competitive P2X7R antagonist (A 438079; Abcam) were dissolved in DMSO (Sigma–Aldrich) and stored at −20 °C.
Chang Y.W., Wang C.C., Yin C.F., Wu C.H., Huang H.C, & Juan H.F. (2022). Quantitative phosphoproteomics reveals ectopic ATP synthase on mesenchymal stem cells to promote tumor progression via ERK/c-Fos pathway activation. Molecular & Cellular Proteomics : MCP, 21(6), 100237.
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