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New England Biolabs
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Rockland Immunochemicals
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Cytoskeleton Inc
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Cytoskeleton Inc
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Danaher Inc
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Rockland Immunochemicals
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Cytoskeleton Inc
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Revvity
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Danaher Inc
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Rockland Immunochemicals
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Rockland Immunochemicals
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Rockland Immunochemicals
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Image Search Results
Journal: Cell reports
Article Title: Cisplatin resistance in an ovarian cancer model is mediated by microtubule dynamics regulator TPPP3 in synergy with tubulin code rewiring
doi: 10.1016/j.celrep.2026.117414
Figure Lengend Snippet: KEY RESOURCES TABLE
Article Snippet: Paclitaxel-stabilized cisplatin sensitive (CP-S) microtubules containing 97% CP-S tubulin, 1% biotin brain tubulin, and 2%
Techniques: Cell-Signaling, Virus, Activation Assay, Control, Recombinant, Labeling, Mass Spectrometry, Sequencing, Cell Viability Assay, DNA Purification, Amplification, CRISPR, Plasmid Preparation, Synthesized, Software, Analysis, Filtration
Journal: STAR Protocols
Article Title: Volumetric super-resolution imaging by serial ultrasectioning and stochastic optical reconstruction microscopy in mouse neural tissue
doi: 10.1016/j.xpro.2021.100971
Figure Lengend Snippet:
Article Snippet: Cy-3B Mono NHS-ester ,
Techniques: Recombinant, Saline, Electron Microscopy, Plasmid Preparation, Software, Imaging, Control, Mass Measurement, Capsules, Microscopy, Staining, Adhesive, Spectrophotometry
Journal: Pharmaceutics
Article Title: Design and Evaluation of Autophagy-Inducing Particles for the Treatment of Abnormal Lipid Accumulation
doi: 10.3390/pharmaceutics14071379
Figure Lengend Snippet: In vivo and organ DiR fluorescence imaging of genetically obese ob/ob mice following a single IV injection (120 µL) of soluble fluorophore or fluorescent particles (0.25% w/v ). ( a ) Autophagy-inducing fluorescent particles (NP DiR T-B) and plain fluorescent particles (NP DiR) accumulate in the liver over the course of 72 h. Images are representative of scans from 3–4 mice per group. ( b ) Quantification of whole-body fluorescence up to 72 h post a single IV injection. The percentage values reported are calculated from the 5 min timepoint, when the maximal fluorescence was observed, and are reported as mean ± s.e.m. Results were analyzed using one-way ANOVA followed by Sidak’s multiple comparison test, which revealed no significant difference between the NP DiR and the NP DiR T-B group for all timepoints. ( c , d ) Organ biodistribution of fluorescent NPs 24 h after a single intravenous (IV) injection in ob/ob mice. n = 3–4 mice per group. Ex vivo DiR fluorescence imaging on main organs (liver, spleen, pancreas and kidneys) ( c ) and quantification of DiR fluorescence ( d ). The percentage values reported are calculated from total organ fluorescence and presented as mean ± s.e.m ( d ).
Article Snippet: Mice were immediately injected in the retro-orbital vein with 120 µL of either
Techniques: In Vivo, Fluorescence, Imaging, IV Injection, Ex Vivo
Journal: Nucleic Acids Research
Article Title: Enhanced exon skipping and prolonged dystrophin restoration achieved by TfR1-targeted delivery of antisense oligonucleotide using FORCE conjugation in mdx mice
doi: 10.1093/nar/gkac641
Figure Lengend Snippet: FORCE–M23D structure, Fab internalization kinetics and FORCE–M23D TfR1 binding affinity in C2C12 mouse myoblasts. ( A ) Schematic representation of the FORCE–M23D conjugate. ( B ) Binding to murine TfR1 with the FORCE–M23D conjugate or with a negative control human-TfR1 specific conjugate by ELISA. ( C ) Uptake of anti-murine TfR1-Cypher5a conjugate and anti-human TfR1-Cypher5e conjugate in C2C12 myoblasts. Data represent mean ± SD. *** P < 0.001. A.U., arbitrary units; ELISA, enzyme-linked immunosorbent assay.
Article Snippet: The pH-sensitive
Techniques: Binding Assay, Negative Control, Enzyme-linked Immunosorbent Assay