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Generate an image of clinical peripheral blood in a purpl... | SciDraw Gallery

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Generate an image of clinical peripheral blood in a purple-top tube, with a white background and no specific cells visible in the blood. Also, generate an image of serum in an Eppendorf tube, with a white background.

Biomedical

Prompt Description

Generate an image of clinical peripheral blood in a purple-top tube, with a white background and no specific cells visible in the blood. Also, generate an image of serum in an Eppendorf tube, with a white background.

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$Generate an image: AI drawing description (for generating a schematic diagram of the DNase-PDA@C-176 microneedle preparation process):\n\nScene Setting:\nA scientific experimental flowchart style, clean, clear, and hierarchical schematic diagram of a laboratory or biomaterial preparation.\n\nImage Content:\nThe left area shows a transparent microneedle mold with neatly arranged conical cavities.\n\nThe middle process is divided into four continuous steps, connected by arrows:\n\nStep 1 (Pouring): A dropper is injecting a mixed solution (HA + DNase-PDA@C-176 NPs) into the mold.\n\nStep 2 (Vacuum): The mold is placed in a vacuum device, bubbles are extracted, and the solution fully fills each cavity.\n\nStep 3 (Drying): The mold is placed in a drying oven or in a ventilated place, and the moisture gradually evaporates.\n\nStep 4 (Demould): A complete microneedle patch (MNs patch) is removed from the mold, with the microneedles neatly arranged.\n\nRight Close-up: Shows a square microneedle patch with 48 cylindrical microneedles (not all need to be drawn), each with a diameter of 600 μm and a length of 1000 μm. A partially enlarged view can be drawn to show that the microneedles are internally encapsulated with nanoparticles (DNase-PDA@C-176 NPs).\n\nLabeling Information: Add concise text labels in appropriate positions in the image, such as:\n\n"HA + DNase-PDA@C-176 NPs mixture"\n\n"Vacuum filling"\n\n"Drying & Demoulding"\n\n"Microneedle patch (48 needles)"\n\nStyle Requirements:\nA flattened or slightly three-dimensional scientific illustration style, with blue, white, and gray as the main colors, and a small amount of highlighted colors (such as light blue or green) to highlight key parts.\n\nClear lines, strong compositional logic, suitable for academic papers or presentation materials.$

Generate an image: AI drawing description (for generating a ...

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Figure creation: MCF7 cell culture. Seeding followed by treatment with five different cellular stressors: 1. Control, 2. Hypoxia (the flask lid was tightly sealed with parafilm), 3. UV Radiation, 4. Serum Depletion (0.5% FBS), 5. Glucose Starvation (low glucose media), 6. DTT/PFA (2 mM DTT and 25 mM PFA). Cells were cultured inside T25 flasks at 37 °C, 5% CO₂ for 48 hours, reaching 80-90% confluence. UV radiation: cells were subjected to five cycles of UV irradiation (5 minutes) followed by incubation (5 minutes) to stimulate the production of multivesicular bodies. Exosome isolation: Samples were centrifuged at 500 × g for 5 minutes at 4 °C, and the supernatant was removed. The cell pellet was resuspended in 5 mL PBS and centrifuged again at 952 rpm for 5 minutes at 4 °C. The pellet was discarded, and the supernatant was retained. Ultracentrifugation: The clarified supernatant was transferred to ultracentrifuge tubes and spun at 100,000 g for 7 minutes.

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