STAT3 cleavage during ES cell differentiation along neural or adipocyte cell lineages

Copyright information:Taken from "Caspase-dependent proteolytic cleavage of STAT3α in ES cells, in mammary glands undergoing forced involution and in breast cancer cell lines"BMC Cancer 2007;7():29-29.Published online 12 Feb 2007PMCID:PMC1800902. Short term differentiation of murine IOUD2...

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Hauptverfasser: Matthews, James R, Watson, Susan MR, Tevendale, Maxine CL, Watson, Christine J, Clarke, Alan R
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Watson, Susan MR
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Clarke, Alan R
description Copyright information:Taken from "Caspase-dependent proteolytic cleavage of STAT3α in ES cells, in mammary glands undergoing forced involution and in breast cancer cell lines"BMC Cancer 2007;7():29-29.Published online 12 Feb 2007PMCID:PMC1800902. Short term differentiation of murine IOUD2 ES cells following removal of LIF for 48 hours. In the adipocyte differentiation protocol, cells were treated with RA between 48 and 72 hours, while cells differentiating along the neural lineage were untreated. Whole cell extracts were immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). 20 day differentiation time course of IOUD2 ES cells along the neural cell lineage. Cells were harvested at the indicated timepoints and whole cell extracts immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). 20 day differentiation time course of IOUD2 ES cells along the adipocyte cell lineage. Cells were harvested at the indicated timepoints and whole cell extracts immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). Arrows indicate cleaved fragments and the asterisk non-specific bands.
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Short term differentiation of murine IOUD2 ES cells following removal of LIF for 48 hours. In the adipocyte differentiation protocol, cells were treated with RA between 48 and 72 hours, while cells differentiating along the neural lineage were untreated. Whole cell extracts were immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). 20 day differentiation time course of IOUD2 ES cells along the neural cell lineage. Cells were harvested at the indicated timepoints and whole cell extracts immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). 20 day differentiation time course of IOUD2 ES cells along the adipocyte cell lineage. 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Short term differentiation of murine IOUD2 ES cells following removal of LIF for 48 hours. In the adipocyte differentiation protocol, cells were treated with RA between 48 and 72 hours, while cells differentiating along the neural lineage were untreated. Whole cell extracts were immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). 20 day differentiation time course of IOUD2 ES cells along the neural cell lineage. Cells were harvested at the indicated timepoints and whole cell extracts immunoblotted with either the anti-STAT3 amino terminal antibody (upper panel, 48 kDa cleaved fragment) or the anti-STAT3 PY705 antibody (lower panel, 43 kDa cleaved fragment). 20 day differentiation time course of IOUD2 ES cells along the adipocyte cell lineage. 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title STAT3 cleavage during ES cell differentiation along neural or adipocyte cell lineages
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