Technical FAQs

      1. How to label particles with dyes?

      In a solution containing hydrophobic dyes, polystyrene particles will expand. Afterwards, this dye can diffuse into the polystyrene matrix. Then the particles are removed from the solvent and dialyzed into the aqueous phase environment, expanding in reverse and embedding the dye into the polystyrene. After the dye is embedded in polystyrene, it will be properly isolated from the external environment.

      2. How many dye molecules are there in a single fluorescent particle?

      We have not determined the specific number of dye molecules in each particle. The number of dye molecules is a variable related to the particle diameter and the properties of the dye.

      3. What is the concentration of the particle product?

      The concentration of particles and other related parameters can generally be found in the corresponding product manual. Most of the instruction manuals can be found on the product webpage. If you can't find it on the webpage, please contact customer service.

      4. I have noticed that most of your particle products contain sodium azide, but my application process cannot contain sodium azide. How can I remove sodium azide from the particle solution?

      We recommend using the method of dialysis with a molecular weight cut-off of 500,000 MWCO to remove sodium azide from the buffer containing particles.

      5. I hope to put the particles into non-aqueous solutions, will they react in alcohols?

      The stability of particles in alcohols or water/alcohol mixtures depends on the chain length of the alcohols. Particles are quite stable in 40% methanol, but they are more soluble in long-chain alcohols. Long-term storage of particles in solvents containing alcohols can lead to the dissolution of dyes.

      6. Do fluorescent particles not contain surfactants?

      Fluorescent particles may contain trace amounts of surfactants. Only latex particles with a diameter greater than 100 nm contain no surfactants at all.

      7. What is the working pH range of the various particles with different surface modifications provided by you?

      We recommend using surface-modified particles within the following pH ranges:
      Modifying group\tAvailable pH range
      Aldehyde/Sulfate\t≥3 and ≤12
      Amino\t ≤9
      Carboxyl\t ≥6 and ≤12
      Sulfate\t ≥3 and ≤12

      8. How to remedy the aggregation of polystyrene particles?

      Unless the particles have been frozen, aggregation is usually reversible under normal circumstances. Before use, the particles can be dispersed by ultrasonic treatment in a water bath ultrasonic instrument. If particles are not used in the living cell system, a low concentration of Tween 20 or Triton X-100 can also be added. For protein-labeled particles, the mildest possible methods should be used to disperse the aggregates to avoid disrupting the protein conformation.
      Note: The smaller the particle size of the particles is, the more likely they are to aggregate.

      9. If PS particles are diluted with PBS solution (1×), will it have an impact on the particles? What if it causes particle agglomeration?

      No.

      10. When the carboxylate-modified latex particles were ultrasonically treated according to the method suggested in the experimental plan, it was found that foam appeared in the solution. Is special attention necessary?

      This situation is normal. The foam is caused by Tween 20, which plays a role in preventing aggregation in the reservoir.

      11. Are fluorescent particles sterile and can they be used for cell experiments?

      It is not sterile and can be filtered through a membrane before use.

      12. Which method should be used to disperse particle aggregates?

      It is recommended to use a water bath ultrasound instrument to disperse aggregates. Do not use the probe ultrasound instrument, otherwise the particles will be damaged.

      13. How to avoid the aggregation of particles?

      All kinds of conditions may lead to the aggregation of particles. Please try to avoid the particles coming into contact with the following environments:
      ①Freezing temperature
      ② Microbial contamination
      ③ High-salt buffer solution
      ④ Extreme pH: Acidic pH can neutralize carboxyl and sulfonate matrix. An alkaline pH will deprotonate the amino group.
      ⑤ Heating, excessive vortexing and excessive ultrasonic treatment: Special attention should be paid to protein-labeled particles.

      14. In the experimental system, non-specific binding occurred in the protein-coated particles. Are there any products that can help reduce these non-specific effects?

      Non-specific binding can be alleviated by blocking solution.

      15. Can frozen particles still be used?

      Even short-term freezing can lead to irreversible aggregation and may cause deformation of the particles, making them unusable.

      16. After washing and centrifugation, only a very small amount of precipitate remained in the particles and the solution was transparent. Why does this phenomenon occur?

      Centrifugation is not an effective method for collecting smaller particles; Even though small precipitates can be seen, there are still quite a few particles remaining in the solution. For particles with a diameter of less than 1 μm, we recommend using any of the following methods for washing:
      ①Cross-flow filtration is carried out because these particles have extremely high compression coefficients and can withstand high gravity without the risk of damage.
      ② Using 500 kDa MWCO to intercept molecular weight for dialysis.
      Note: Particles with a diameter greater than 1 μm can be centrifuged at 1,300 rpm.

      17. My particles have been in use for over a year. I wonder if they are still usable. What is a good way to check its function?

      Bacterial contamination is the most common cause that makes particles unusable. Many of our particles contain low levels of sodium azide to prevent bacterial contamination, but this still happens sometimes. The best way to assess bacterial contamination is to perform electroplating on an appropriate medium and conduct an inspection after 72 h.

      18. The reason why the density of PE is 0.94-0.96, while the density of PE particles is 1.1.

      PE particles were prepared by the template method, PS was used as the framework, and the PE content was above 75%. At present, 100% pure PE particles cannot be provided. There is also the crosslinking agent divinylbenzene. Therefore, the density will be large. Cross-linking will lead to a higher density.

      19. If the fluorescence of the fluorescent particles is monitored for at least 3 min, will they gradually quench?

      No.

      20. What is the construction environment for rare earth europium PVC particles?

      PVC wrapping.