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Table 1.

Subgrouping of medulloblastomas based on the evaluation of IHC immunoreactivity for selected protein markers [13].

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Table 1 Expand

Table 2.

Description of the patient cohort and patient-derived cell lines.

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Table 2 Expand

Table 3.

Antibodies used in this study.

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Table 3 Expand

Fig 1.

Immunohistochemical detection of selected protein markers in tumor samples.

Expression of β-catenin, filamin A, GAB1 and YAP1 in medulloblastoma tissue samples (1–6) as detected by immunohistochemistry. Bars, 100 μm.

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Fig 1 Expand

Table 4.

Analysis of the expression and intracellular localization of selected protein markers in tumor samples and corresponding cell lines.

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Table 4 Expand

Fig 2.

Immunofluorescence detection of selected protein markers in corresponding cell lines.

Expression of β-catenin, filamin A, GAB1 and YAP1 in medulloblastoma cell lines as detected by IF. Each marker was visualized by indirect immunofluorescence using Alexa 488-conjugated secondary antibody (green); nuclei were counterstained with DAPI (blue). Bars, 50 μm (β-catenin, filamin A, YAP1) or 20 μm (GAB1).

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Fig 3.

Immunoblot analysis of selected protein markers in medulloblastoma cell lines.

Expression of β-catenin, filamin A, GAB1 and YAP1 in patient-derived and reference medulloblastoma cell lines as detected by immunoblotting. β-actin served as a loading control.

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Fig 3 Expand