email

Email:

info@biotech-pack.com

Free Quote
百泰派克蛋白质测序
百泰派克蛋白质组学服务
百泰派克生物制药分析服务
百泰派克代谢组学服务

Who knows about the preparation of Western blot protein gels? There are always a lot of bubbles on the edge, everything else is normal, begging for help from the great gods?

When preparing protein gels for Western blotting, the occurrence of many bubbles around the edges may be due to the following reasons:

1. Bubbles during gel solution preparation:

During the preparation of polyacrylamide gel, if the gel solution is not thoroughly mixed or stirred evenly, bubbles may be generated. To avoid this, ensure thorough stirring during gel solution preparation and let the solution stand for a while before use to allow bubbles to rise and disappear.

2. Bubbles during gel solution injection:

When injecting the gel solution into the gel plate, if the injection speed is too fast or if care is not taken to avoid bubble formation, bubbles can become trapped in the gel. To prevent this, inject the gel solution slowly and use tools like syringes carefully to avoid bubble formation.

3. Inadequate sealing of the gel plate:

If the gel plate is not sealed properly, air can enter the gel solution and form bubbles. To prevent this, apply a layer of sealing gel around the gel plate or use a specialized gel plate sealant to ensure proper sealing.

4. Contaminants in the gel solution:

If there are contaminants in the gel solution, such as dust or bacteria, bubbles may form. To avoid this, filter the gel solution using a filter to remove suspended particles before preparation.

5. Inappropriate pH value of the gel solution:

If the pH value of the gel solution is too high or too low, it may lead to bubble formation. Use a pH meter to measure the pH value of the gel solution and adjust it as necessary.

BiotechPack, A Biopharmaceutical Characterization and Multi-Omics Mass Spectrometry (MS) Services Provider

Related Services:

Far-Western Blot analysis

Protein interaction analysis

Protein interaction mass spectrometry analysis

Protein interaction analysis using co-immunoprecipitation (CO-IP) combined with mass spectrometry

Protein interaction analysis using GST fusion protein Pull-down technology combined with mass spectrometry

Protein interaction analysis using SILAC combined with co-immunoprecipitation and mass spectrometry

Cross-linking method protein interaction analysis

Label transfer method protein interaction analysis

Pull-down target protein mass spectrometry identification

Submit Inquiry
Name *
Email Address *
Phone Number
Inquiry Project *
Project Description*

 

How to order?