Gel Documentation System LBGD-T2010

Introduction

Gel Documentation System is a close-packed vertical gel documentation system designed for nucleic acids and proteins quantification. Equipped with 16-bit high-resolution power and a highly sensitive camera to capture the gel images efficiently. The captured images can be easily saved for later analysis in varied formats. Integrated with UV and white light transilluminators to visualize samples.

This gel documentation is designed to meet the rigorous requirements of modern laboratory operations, ensuring high precision, reliability, and ease of use for various experimental applications.

Applications

Gel Documentation System is mainly used in molecular biology laboratories for imaging and documentation of nucleic acid, proteins, various fluorescent dyes, silver-stained glue, deep purple and Pro-Q Diamond, labelling glue/membrane/chip.

Specifications

camera	Scientific Digital Camera
Resolution	5 megapixels, 2592×1944
Pixel density	16-bit (65536 Grey scales)
High QE	0.75
Readout Noise	5.1e-
Signal to Noise ratio	70.1db
Sensitivity	10pg EB-stained
Lens	F1.2 motorized lens
Light Source	White light ×2
Packaging Dimension	500 x 550 x 880 mm
Net Weight	22 Kg
Gross Weight	26 Kg

Features

Built-in UV transilluminator provides clear visualization of fluorescent dye-stained samples

Offers the analysis of the colorimetric samples using a White light transilluminator

Designed with a scientific high-resolution camera for precise and sharp images

An easy-to-open and close door design ensures smooth operation

Equipped with easily removable and attachable plate

Smartly designed intuitive software simplifies image processing, analysis and quantification

FAQs

1. What are the key factors to consider when selecting this gel documentation for laboratory use?

When selecting this gel documentation, key factors include: 1) The instrument's precision and accuracy to meet experimental requirements; 2) Compatibility with the types of samples and applications you will be working with; 3) Ease of use and maintenance requirements; 4) Safety features to protect operators and samples; 5) Calibration and certification requirements; 6) Cost-effectiveness and long-term reliability; 7) Technical support and service availability from the supplier. Evaluating these factors ensures that the instrument meets your laboratory's specific needs.

2. How often should this gel documentation be calibrated to ensure accurate results?

It is recommended to calibrate this gel documentation at least once every 6-12 months under normal usage conditions. More frequent calibration (every 3-6 months) may be necessary if: 1) The instrument is used continuously for extended periods; 2) It is exposed to harsh environmental conditions (temperature fluctuations, humidity, dust); 3) It is used for critical applications requiring high precision; 4) The instrument has been moved or subjected to physical shock; 5) Calibration checks indicate significant deviations from standard values. Always follow the manufacturer's calibration guidelines.

3. What are the common maintenance procedures required for this gel documentation?

Common maintenance procedures include: 1) Regular cleaning of the instrument's exterior and sample contact surfaces to prevent contamination and ensure proper operation; 2) Inspection of moving parts (if applicable) for wear and lubrication as recommended by the manufacturer; 3) Replacement of consumable parts (filters, bulbs, reagents) according to usage guidelines; 4) Verification of performance parameters (temperature, pressure, voltage) regularly; 5) Storage of the instrument in a clean, dry environment when not in use; 6) Keeping a maintenance log to track service activities and identify potential issues early; 7) Following the manufacturer's specific maintenance schedule for optimal performance and longevity.

4. Can this gel documentation be used with different types of samples, and are there any compatibility considerations?

Yes, this gel documentation can be used with a variety of sample types, but compatibility considerations are important: 1) Check if the instrument's materials are compatible with the chemical composition of your samples (avoid corrosive or reactive substances that may damage the instrument); 2) Ensure that the sample volume and concentration are within the instrument's recommended range; 3) For biological samples, consider sterility requirements and potential cross-contamination risks; 4) For volatile or hazardous samples, ensure proper ventilation and safety precautions are in place; 5) Consult the manufacturer's documentation for specific sample compatibility guidelines, and perform compatibility tests with new sample types before regular use.

5. What should be done if the gel documentation malfunctions or produces inconsistent results?

If malfunctions or inconsistent results occur: 1) First, check the instrument's user manual for troubleshooting guidelines specific to the issue; 2) Verify that the instrument is properly calibrated and within its calibration period; 3) Inspect for obvious issues such as loose connections, damaged parts, or incorrect settings; 4) Clean the instrument thoroughly to remove any contamination that may affect results; 5) Repeat the experiment with a known standard sample to determine if the issue is with the instrument or the sample; 6) If the problem persists, discontinue use of the instrument to prevent further damage or inaccurate results; 7) Contact technical support or a qualified service technician for diagnosis and repair, providing details of the issue and any troubleshooting steps already performed.