Illustration
Visualization
Convert Image
Pricing
Blog

SciDraw

AI-powered scientific illustration platform for researchers and PhD students. Create publication-ready TOC graphics, journal covers, conference posters, and research figures in minutes. No design skills required.

Email Stripe Climate

Stripe Climate Contribution

Product

Features
Pricing
Gallery

Blog

Product
Tutorials
Changelog

Legal

Cookie Policy
Privacy Policy
Terms of Service

© 2026 SciDraw All Rights Reserved.

A Transwell image, 6-well plate. | SciDraw Gallery

Back to Gallery

A Transwell image, 6-well plate.

Biomedical

Prompt Description

A Transwell image, 6-well plate.

Related Illustrations

Mulching enhances pre-anthesis aboveground nitrogen accumulation (primarily concentrated in reproductive organs) by shortening Tm,so and increasing Sso, and promotes nitrogen redistribution (NRA, NRE, and CRN, with the contribution of each organ ranked as glume > stem > leaf), thereby increasing the grain nitrogen accumulation rate (Ssi and Smax,si) and ultimately improving protein yield. Drip irrigation slightly promoted wheat nitrogen uptake (NUA, CUA, and CUN) during the grain filling stage, but also prolonged the grain filling duration (increased Te,si) and reduced the grain nitrogen accumulation rate (Ssi and Smax,si), resulting in increased protein yield only in 2024. 50% full irrigation enhanced pre-anthesis nitrogen redistribution, especially increasing NRA in leaves and glumes, and promoted post-anthesis nitrogen accumulation by increasing source (Nmax,so, Sso, and Smax,so) and sink (Nmax,si, Ntm,si, and Ssi), thereby accelerating grain maturation. Correlation analysis, principal component analysis, and linear regression models consistently indicated that higher protein yield was significantly correlated with enhanced NRA and Sso, and shortened Tm,so.

Mulching enhances pre-anthesis aboveground nitrogen accumula...

Core Instruction: Create a clear, modular scientific diagram illustrating the multi-layered regulation of ERF proteins.

1. Overall Composition and Layout

Style: Flat vector graphics, using clear lines and blocks of color. Academic cartoon style.

Layout: Employ a core-periphery radial layout.

Canvas: Horizontal rectangular canvas with a white background.

2. Central Core: ERF Protein Binding to DNA (placed in the center of the image)

Draw a light gray DNA double helix fragment, placed horizontally.

On the DNA, highlight the "GCC-box" sequence (5'-GCCGCC-3') in yellow.

Draw the ERF protein: Represent it with a soft blue irregular shape (symbolizing the protein). Inside this shape:

Highlight a core region in dark blue, labeled "AP2/ERF DNA-Binding Domain." This dark blue region should be directly embedded in and in contact with the DNA's GCC-box, indicating binding.

In the upper region of the blue protein shape, draw an orange "flame" or "starburst" shape, labeled "Activation Domain (AD)."

In the lower region of the blue protein shape, draw a gray "square lock" or "inhibition symbol" shape, labeled "Repression Domain (e.g., EAR)."

3. Peripheral Module One: Transcriptional Control (placed above the center)

Left: Draw several small molecule icons—ethylene (two connected spheres with a double bond in the middle), ABA (a polycyclic structure), and a light icon (sun).

Middle: Draw a gene structure diagram. A rightward arrow represents "ERF Gene Promoter," followed by a rectangular box (representing "ERF Gene"), and then a lightning symbol representing transcription producing "ERF mRNA."

Right: Draw a ribosome icon and a small protein icon.

Connection: Connect from left to right with dashed arrows: Signal molecules → Gene promoter → ERF gene → mRNA → Protein. Label the arrow: Transcriptional Control.

4. Peripheral Module Two: Post-translational Modifications (placed to the right of the center)

Next to the central ERF protein, draw two dynamic processes:

Phosphorylation: Draw a red circle with "P" inside, with an arrow pointing from a kinase icon (a small enzyme encapsulating ATP) to a specific location on the ERF protein.

Ubiquitination: Draw a small yellow sphere labeled "Ub." Draw an E3 ligase icon connecting a series (e.g., 3) of "Ub" spheres to the ERF protein. An arrow points from the ubiquitinated ERF to a proteasome (barrel-shaped structure).

Add the title above this module: Post-translational Modifications.

5. Peripheral Module Three: Protein Interaction Network (placed below the center)

Centered on

Core Instruction: Create a clear, modular scientific diagram...

Alzheimer's disease is characterized by cognitive decline, memory loss, and neuroinflammation, with acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) identified as therapeutic targets. This study evaluated the in vitro and in silico anticholinesterase activity, as well as the cytotoxicity, of the essential oils of Eplingiella fruticosa and Medusantha martiusii. The oils were extracted via hydrodistillation and analyzed by GC-MS. In vitro evaluation revealed that both oils exhibited greater activity against BuChE than AChE. The oils demonstrated significant inhibition and selectivity, with IC50 values ranging from 29.2 to 612.1 µg/mL. Molecular docking studies indicated strong interactions between thymol and eudesm-7(11)-en-4-ol with the target enzymes. M. martiusii exhibited higher activity and lower cytotoxicity (IC50 of 876.5 µg/mL) compared to E. fruticosa (574.3 µg/mL). These findings highlight the dual anticholinesterase activity of these essential oils, particularly M. martiusii, which demonstrated promising selectivity for BuChE and lower cytotoxicity.

Alzheimer's disease is characterized by cognitive decline, m...

Background and aim: This study evaluates the effects of the Sahatsatara formula (STF) on platelet aggregation and examines associations with the Thai birth Dhatu Chao Ruean (bDCR) element classification. Experimental procedure: Forty healthy volunteers (20 male, 20 female) were assigned to Earth, Water, Wind, or Fire groups based on their birth month according to bDCR. Participants received STF (5 capsules three times daily, 30 minutes before meals) for 7 days. Platelet aggregation was measured by light transmission aggregometry at baseline and on days 1 and 7. Platelet cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) mRNA and protein levels, as well as plasma thromboxane B2 (TXB2), were quantified using real-time polymerase chain reaction, Western blot, and enzyme-linked immunosorbent assay. Results: On day 1, collagen-induced aggregation decreased significantly in a subgroup exhibiting disaggregation patterns; values returned to baseline by day 8. Individuals classified as Earth element exhibited reduced COX-1 mRNA expression (P < 0.05).

Background and aim: This study evaluates the effects of the ...