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Cellvis Inc glass bottom dishes
Glass Bottom Dishes, supplied by Cellvis Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glass+bottom+dishes/bottom+dishes+glass/pm42314170-78-46-48
Average 86 stars, based on 1 article reviews
glass bottom dishes - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

other:

Article Title: IQGAP3 bridges matrix stiffness with glioma stem cell maintenance and radioresistance by stabilizing SOX2.
Article Snippet: Glass-bottom dishes (Cellvis, D35–14-1-N and D60-30-1-N) were prepared for gel attachment by treating them with 100~200 μl of Bind-Silane solution for 20 minutes at room temperature.

Imaging:

Article Title: Glutamatergic neuron-tumor synapses shape human glioblastoma cell states through radial glia plasticity
Article Snippet: .. For live imaging, organoid slices were mounted onto 35-mm glass-bottom dishes (Cellvis) using 1% low-melting point agarose (Millipore Sigma) in PBS. .. For slice preparation, organoids were embedded in 3% low-melting point agarose (Precisionary Instruments) in basal DMEM and sectioned using a Compresstome VF-510-0Z (Precisionary Instruments).

Transfection:

Article Title: Engineered Lysosome-Targeted Protein Degradation via Hijacking Macropinocytosis.
Article Snippet: Recently, targeted protein degradation (TPD) strategies have emerged as an effective tool for addressing undruggable targets in both biomedical research and the pharmaceutical industry, selectively binding proteins of interest and targeting them to the intracellular degradation machinery for degradation.. However, the targeting of extracellular proteins with current degradation tools requires a tedious, case-specific selection and design process based on lysosomal trafficking of cell surface receptors.. Here, we introduce Macropinocytosis-Targeting Chimeras (MapTACs), a TPD platform that exploits macropinocytosis, a receptor-independent endocytic process, to deliver extracellular proteins to lysosomes for degradation.

Article Title: C-terminal long-QT type 1 R562S-Kv7.1 variant, the first variant in helix C impairing β-adrenergic response of the slow delayed rectifier K+ channel.
Article Snippet: 20 For the fluorescence image acquisition, a confocal laser scanning microscope Leica 21 TCS SP8 X (Leica Microsystems, Wetzlar, Germany) was used. .. WT and R562S human 22 KCNQ1 tagged with green fluorescent protein (GFP) at the 3'-terminus were transfected 23 AC CE PT ED M AN US CR IP T D ow nloaded from https://academ ic.oup.com /europace/advance-article/doi/10.1093/europace/euag156/8711184 by guest on 21 June 2026 into CHO cells seeded on glass-bottom dishes (Cellvis, Mountain View, CA, USA) coated 1 with fibronectin ~48 hours before the evaluation (KCNQ1 and KCNE1 in the molar ratio 1:2). ..

Expressing:

Article Title: Engineered Lysosome-Targeted Protein Degradation via Hijacking Macropinocytosis.
Article Snippet: Recently, targeted protein degradation (TPD) strategies have emerged as an effective tool for addressing undruggable targets in both biomedical research and the pharmaceutical industry, selectively binding proteins of interest and targeting them to the intracellular degradation machinery for degradation.. However, the targeting of extracellular proteins with current degradation tools requires a tedious, case-specific selection and design process based on lysosomal trafficking of cell surface receptors.. Here, we introduce Macropinocytosis-Targeting Chimeras (MapTACs), a TPD platform that exploits macropinocytosis, a receptor-independent endocytic process, to deliver extracellular proteins to lysosomes for degradation.



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