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Anti human max mouse monoclonal

Manufactured by Abcam
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The Anti-human MAX mouse monoclonal is a laboratory reagent used to detect the MAX protein, which is a transcription factor involved in cellular processes. This product is suitable for use in various research applications, such as Western blotting, immunohistochemistry, and immunocytochemistry.

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Lab products found in correlation

Polyvinylidene diflouride membrane, by Merck Group (2 mentions) Anti human cdk2 rabbit monoclonal, by Cell Signaling Technology (2 mentions) Anti human cdk4 mouse monoclonal, by Cell Signaling Technology (2 mentions) Anti human c myc rabbit monoclonal d84c12, by Cell Signaling Technology (2 mentions) Anti human p53 mouse monoclonal clone 1c12, by Cell Signaling Technology (2 mentions) Anti beta actin hrp conjugated monoclonal, by Santa Cruz Biotechnology (2 mentions) Anti gapdh hrp conjugated monoclonal antibody, by Santa Cruz Biotechnology (2 mentions) Hrp conjugated goat anti rabbit or anti mouse secondary antibodies, by Santa Cruz Biotechnology (2 mentions)

Close spelling variants of this product

Monoclonal mouse Mouse anti

2 protocols using anti human max mouse monoclonal

1

Western Blot Analysis of Cell Signaling Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
Western blottng was performed as previously described. Protein was transferred to polyvinylidene diflouride membranes (Millipore) and immunoblotted with anti-human CDK2 rabbit monoclonal, anti-human CDK4 mouse monoclonal, anti-human c-Myc rabbit monoclonal (D84C12), or anti-human p53 mouse monoclonal (clone:1C12) antibodies (all at 1:2000; Cell Signaling). Additional antibodies included anti-human MAX mouse monoclonal (1:2000; Abcam), anti-beta Actin HRP conjugated monoclonal (1:5000; Santa Cruz), or anti-GAPDH HRP conjugated monoclonal antibody (1:2000; Santa Cruz) for at least 1h at room temperature or 4°C overnight. HRP–conjugated goat anti-mouse or anti-rabbit secondary antibodies (Santa Cruz) were added when needed.
Lu Y.C., Sanada C., Xavier-Ferrucio J., Wang L., Zhang P.X., Leighton Grimes H., Venkatasubramanian M., Chetal K., Aronow B., Salomonis N, & Krause D.S. (2018). The Molecular Signature of Megakaryocyte-Erythroid Progenitors Reveals a Role for the Cell Cycle in Fate Specification. Cell reports, 25(8), 2083-2093.e4.
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2

Western Blot Analysis of Cell Signaling Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
Western blottng was performed as previously described. Protein was transferred to polyvinylidene diflouride membranes (Millipore) and immunoblotted with anti-human CDK2 rabbit monoclonal, anti-human CDK4 mouse monoclonal, anti-human c-Myc rabbit monoclonal (D84C12), or anti-human p53 mouse monoclonal (clone:1C12) antibodies (all at 1:2000; Cell Signaling). Additional antibodies included anti-human MAX mouse monoclonal (1:2000; Abcam), anti-beta Actin HRP conjugated monoclonal (1:5000; Santa Cruz), or anti-GAPDH HRP conjugated monoclonal antibody (1:2000; Santa Cruz) for at least 1h at room temperature or 4°C overnight. HRP–conjugated goat anti-mouse or anti-rabbit secondary antibodies (Santa Cruz) were added when needed.
Lu Y.C., Sanada C., Xavier-Ferrucio J., Wang L., Zhang P.X., Leighton Grimes H., Venkatasubramanian M., Chetal K., Aronow B., Salomonis N, & Krause D.S. (2018). The Molecular Signature of Megakaryocyte-Erythroid Progenitors Reveals a Role for the Cell Cycle in Fate Specification. Cell reports, 25(8), 2083-2093.e4.
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