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plasma membrane protein isolation kit  (Invent Biotechnologies)


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    Invent Biotechnologies plasma membrane protein isolation kit
    Plasma Membrane Protein Isolation Kit, supplied by Invent Biotechnologies, used in various techniques. Bioz Stars score: 96/100, based on 611 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 96 stars, based on 611 article reviews
    plasma membrane protein isolation kit - by Bioz Stars, 2026-05
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    A. IHC staining for WEE1 in Human EAC tissue sections depicting strong cytosolic localization B. Quantification of the Cytoplasmic and Nuclear Signals from A using Cell Profiler C. Cell <t>fractionation</t> of FLO1 and OE33 EAC cell lines followed by western blot for WEE1, p84 (Nuclear marker) and ὰ-Tubulin (Cytoplasmic marker) D- Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (Blue) in EAC cell lines FLO1 and OE33, captured at 40X Magnification.E.MYC mRNA expression in WEE1 high Vs WEE1 low EAC tissue samples derived from TCGA and 4 different GEO datasets. F. Gene Set Enrichment Analysis (GSEA) of MYC target genes in WEE1 high Vs WEE1 low EAC samples G. WEE1 mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001. H. MYC mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . I. Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (blue) in normal esophagus and gastroesophageal adenocarcinoma tissue sections in TMA, captured at 20x magnification. J- Quantification of fluorescence intensity from I K – Correlation analysis between WEE1 and MYC signal intensity
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    Invent Biotechnologies plasma membrane protein isolation kits
    A. IHC staining for WEE1 in Human EAC tissue sections depicting strong cytosolic localization B. Quantification of the Cytoplasmic and Nuclear Signals from A using Cell Profiler C. Cell <t>fractionation</t> of FLO1 and OE33 EAC cell lines followed by western blot for WEE1, p84 (Nuclear marker) and ὰ-Tubulin (Cytoplasmic marker) D- Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (Blue) in EAC cell lines FLO1 and OE33, captured at 40X Magnification.E.MYC mRNA expression in WEE1 high Vs WEE1 low EAC tissue samples derived from TCGA and 4 different GEO datasets. F. Gene Set Enrichment Analysis (GSEA) of MYC target genes in WEE1 high Vs WEE1 low EAC samples G. WEE1 mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001. H. MYC mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . I. Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (blue) in normal esophagus and gastroesophageal adenocarcinoma tissue sections in TMA, captured at 20x magnification. J- Quantification of fluorescence intensity from I K – Correlation analysis between WEE1 and MYC signal intensity
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    Invent Biotechnologies cell fraction kit
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    Invent Biotechnologies endosome isolation
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    A. IHC staining for WEE1 in Human EAC tissue sections depicting strong cytosolic localization B. Quantification of the Cytoplasmic and Nuclear Signals from A using Cell Profiler C. Cell fractionation of FLO1 and OE33 EAC cell lines followed by western blot for WEE1, p84 (Nuclear marker) and ὰ-Tubulin (Cytoplasmic marker) D- Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (Blue) in EAC cell lines FLO1 and OE33, captured at 40X Magnification.E.MYC mRNA expression in WEE1 high Vs WEE1 low EAC tissue samples derived from TCGA and 4 different GEO datasets. F. Gene Set Enrichment Analysis (GSEA) of MYC target genes in WEE1 high Vs WEE1 low EAC samples G. WEE1 mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001. H. MYC mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . I. Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (blue) in normal esophagus and gastroesophageal adenocarcinoma tissue sections in TMA, captured at 20x magnification. J- Quantification of fluorescence intensity from I K – Correlation analysis between WEE1 and MYC signal intensity

    Journal: Cancer letters

    Article Title: WEE1 Stabilizes MYC to Promote Therapeutic Resistance in Esophageal Adenocarcinoma

    doi: 10.1016/j.canlet.2026.218418

    Figure Lengend Snippet: A. IHC staining for WEE1 in Human EAC tissue sections depicting strong cytosolic localization B. Quantification of the Cytoplasmic and Nuclear Signals from A using Cell Profiler C. Cell fractionation of FLO1 and OE33 EAC cell lines followed by western blot for WEE1, p84 (Nuclear marker) and ὰ-Tubulin (Cytoplasmic marker) D- Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (Blue) in EAC cell lines FLO1 and OE33, captured at 40X Magnification.E.MYC mRNA expression in WEE1 high Vs WEE1 low EAC tissue samples derived from TCGA and 4 different GEO datasets. F. Gene Set Enrichment Analysis (GSEA) of MYC target genes in WEE1 high Vs WEE1 low EAC samples G. WEE1 mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001. H. MYC mRNA expression in non-cancerous normal esophagus (Normal) and Esophageal cancer (Tumor) tissue samples, analyzed by TNM plot.com . I. Co-Immunofluorescence of WEE1 (green) and C-MYC (Red) along with DAPI nuclear stain (blue) in normal esophagus and gastroesophageal adenocarcinoma tissue sections in TMA, captured at 20x magnification. J- Quantification of fluorescence intensity from I K – Correlation analysis between WEE1 and MYC signal intensity

    Article Snippet: Cell fractionation in FLO1 and OE33 cell lines was carried out according to the protocol described in the Cell Fractionation Kit (CST).

    Techniques: Immunohistochemistry, Cell Fractionation, Western Blot, Marker, Immunofluorescence, Staining, Expressing, Derivative Assay, Fluorescence