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Immunocytochemistry to study myogenesis in zebrafish.

Methods in molecular biology (Clifton, N.J.) (2011-12-02)
Nathan C Bird, Stefanie E Windner, Stephen H Devoto
要旨

During myogenesis, cells gradually transition from mesodermal precursors to myoblasts, myocytes, and then to muscle fibers. The molecular characterization of this process requires the ability to identify each of these cell types and the factors that regulate the transitions between them. The most versatile technique for assaying cell identities in situ is immunocytochemistry, because multiple independent molecular markers of differentiation can be assayed simultaneously. The zebrafish has developed into a popular model for the study of myogenesis, and immunocytochemical techniques have been critical. We have adapted existing protocols to optimize immunocytochemistry in zebrafish, and have tested many antibodies developed against mouse, chick, and frog muscle antigens for their cross-reactivity in zebrafish. Here, we present protocols for whole mount immunocytochemistry on both formaldehyde and Carnoy's fixed embryos as well as on sectioned zebrafish tissue. We include a table of antibodies useful for experiments on the molecular biology of myogenesis in zebrafish.

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製品内容

Sigma-Aldrich
抗ラミニン ウサギ宿主抗体, 0.5 mg/mL, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
抗β-カテニン ウサギ宿主抗体, whole antiserum
Sigma-Aldrich
抗デスミン ウサギ宿主抗体, whole antiserum
Sigma-Aldrich
モノクローナル抗β-カテニン マウス宿主抗体, clone 15B8, ascites fluid
Sigma-Aldrich
モノクロナール抗トロポミオシン(筋節) マウス宿主抗体, clone CH1, ascites fluid
Sigma-Aldrich
モノクロナール抗ジストロフィン マウス宿主抗体, clone MANDRA1, ascites fluid