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Anti mitf antibody

Manufactured by Santa Cruz Biotechnology
Sourced in United States

The Anti-MITF antibody is a tool used in research applications to detect and study the MITF (Microphthalmia-associated transcription factor) protein. MITF is a key regulator of pigment cell development and function. This antibody can be used in various techniques, such as Western blotting, immunohistochemistry, and immunocytochemistry, to identify and analyze the MITF protein in biological samples.

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2 protocols using anti mitf antibody

1

Melanin Signaling Pathway Regulation

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Example 2

Melanocytes (B16F10 cell line) were incubated on 6-well culture plates in an incubator for 24 hours, and were treated with the peptide of the present invention with different concentrations. After the cells were incubated for from 6 to 24 hours, the cells were dissolved, and then the CREB phosphorylation and MITF expression, which are signaling molecules involved in melanogenesis, were observed by western blot assay using antibodies specific thereto. The test was carried out using anti-pCREB antibody (Santa Cruz Biotechnology, USA) and anti-MITF antibody (Santa Cruz Biotechnology, USA).

When mouse melanocytes B16F10 were treated with the peptide having the amino acid sequence of SEQ ID NO: 1 or SEQ ID NO: 2, and then the changes in expressions of the melanin signaling molecules were observed over time, the phosphorylation levels of MITF, which is a transcription factor to increase the expression of a melanogenic enzyme, and CREB, which increases the expression of MITF, were increased (FIGS. 2a and 2b).

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2

Western Blot Analysis of Transcription Factors

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Whole-cell extracts (10 μg/lane) or nuclear extracts were prepared using the method of Schreiber, E. et al.(19 (link)) and then subjected to Western blotting analysis using anti-SOX10 antibody (Santa Cruz), anti-MITF antibody (C5), anti-IRF4 antibody (Santa Cruz), anti-IRF1 antibody (Cell Signaling Technology, Danvers, MA, USA), anti-α-tubulin antibody (Sigma), or anti-Histone H3 antibody (Abcam). The band intensities were measured by ImageJ and normalized to that of each control lane.
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