Chemiluminescence Imaging System SCG-W3000

SCG-W3000 Chemiluminescence Imaging System

SCG-W3000 chemiluminescence imaging system is equipped with a high-sensitivity camera with 9 million pixels. It enables fast, accurate, and high-throughput detection and imaging of samples, and is widely used in fields such as life sciences, medicine, and environmental protection.

1. Whether the signal is weak or strong, a single imaging session can deliver your WB results.
   • For weak signals, you can directly extend the imaging time based on the original image for further imaging.
   • For strong signals, you can adjust the timeline to retrieve any result image from the imaging duration.
2. Supports simultaneous imaging of up to 10 membranes (or even more), improving instrument efficiency—1 device equals 10!
3. Dual-camera system:
   • A color camera captures markers with true-to-life colors for greater authenticity.
   • A monochrome camera captures bands with high sensitivity, delivering superior performance for weak signals.
4. Marker optimization function:
   • Eliminates nonspecific band signals caused by prestained markers and antibody interactions.
   • Adjusts overexposed or underexposed chemiluminescent marker signals.
5. Source file storage allows flexible adjustments anytime:
   • If bands appear too thick or too thin after the experiment, you can easily fine-tune the results on your computer using the source file function!

Working with the ECL Chemiluminescence Kit (G2161-200ML), it meets the exposure needs of high, medium, and low-concentration samples. Enjoy a better WB imaging process and achieve superior WB imaging results!

SWE Imaging Grayscale Analysis Software-SCG-W2000 SCG-W3000-3.3.2-win32-x64-setup.exe

Download link from Google Drive: https://drive.google.com/file/d/1IoXazML9PDHoN4HqOYm-t3C2bVFvQ_rt/view?usp=drive_link

SOFTWARE USER MANUAL:

SWE Imaging Grayscale Analysis Software-SCG-W2000 SCG-W3000.pdf

Notes:

1. Do not touch or scratch the internal lens of the dark box with hands or sharp objects.
2. After placing the sample, ensure the instrument door is properly closed to prevent external light from entering and affecting results.
3. During imaging, avoid shaking the workbench or instrument to prevent compromised image quality.
4. Observe electrical safety—do not pull the power cord or move the instrument during operation.
5. After experiments, clean the dark box thoroughly, removing all samples and residues.

Parameter Comparison

Literature Citations:

• Wang G., et al. An injectable decellularized extracellular matrix hydrogel with cortical neuron-derived exosomes enhances tissue repair following traumatic spinal cord injury. Mater Today Bio 28, 101250 (2024). PMID 39318371 IF 8.2 (PMID:39318371)

• Liu, S., et al. PTGES3 proteolysis using the liposomal peptide-PROTAC approach. Biol Direct 19, 144 (2024). PMID 39726032 IF 5.7 (PMID:39726032)

• Huang, K., et al. The Role of TPM3 in Protecting Cardiomyocyte from Hypoxia-Induced Injury via Cytoskeleton Stabilization. Int J Mol Sci 25, 25 (2024). PMID 38928503 IF 5.

• Zhang,​​​​​ PMID:40427372

• Tan, C., et al. Lycopene inhibits pyroptosis of endothelial progenitor cells induced by ox-LDL through the AMPK/mTOR/NLRP3 pathway. Open Med (Wars) 2024, 20240973 (2024). PMID 38919547 Application: WB IF 2.1