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Hydrogel
- What is VitroGel®?
- Which VitroGel® hydrogel product should I choose?
- Does VitroGel® have viscoelastic properties?
- Will adjusting the temperature induce the hydrogel formation of VitroGel®?
- Can molecules penetrate or diffuse through VitroGel®?
- Does VitroGel® have autofluorescence?
- Can I harvest cells after culturing with VitroGel®?
- Can VitroGel® be used for both 3D culture and 2D hydrogel coating? Which culture method should I choose?
- Is VitroGel® biocompatible for in vivo study?
- How long can cells be grown in the VitroGel® system?
- What are the differences between the 4 VitroGel® ORGANOID versions?
- What are the different mechanical strengths between VitroGel® ORGANOID versions?
- Which VitroGel® ORGANOID hydrogel should I choose for my organoid type?
- Can VitroGel® perform transfection studies?
- Can DMSO be used with the VitroGel®? If so, what is the maximum amount of DMSO that can be mixed with the hydrogel?
- Do I need to keep the VitroGel®-Cell mixture in an ice bucket?
- How long does the VitroGel®-Cell mixture retain its injectable status compared to Matrigel?
- After injection with VitroGel®, how efficient is cell retention?
- How does gelation work in VitroGel®?
- How do I adjust the hydrogel formation time?
- What can I do to prevent bubbles from forming when mixing the VitroGel® solution with the cell culture medium?
- Can I add extracellular matrix proteins or other molecular compounds into VitroGel®?
- Why does the hydrogel sticks loosely to the tissue culture plate?
- Can I use a serum-free medium with VitroGel® ?
- Is it possible to dilute VitroGel® hydrogels with cell culture medium instead of the dilution solution?
- How do I prepare the cell suspension to mix with the hydrogel? Should I add serum?
- What is the optimal incubation time?
- What is the optimal ratio between cell suspension and gel for the mix?
- What is the stiffness of the ready-to-use VitroGel® hydrogels?
- Are the functional ligands such as RGD conjugated (or tethered) on the VitroGel® polymer?
- Are there visual or other methods can be used to verify the status of hydrogel formation?
- How stable of VitroGel® Microbead in cell culture medium?
- Can we use the same cell seeding number of Matrigel for VitroGel® system?
- Do you have suggestions for preventing hydrogel detaching during multiple washing process?
- Do you have the SEM protocol for VitroGel®?
- Can I use VitroGel® for Spheroid Invasion Assay? What is the protocol?
- How do you crosslink the bioink after printing?
- How long are the cell culture models stable?
- What principal component is used in VitroINK®?
- Can I do histology and immunofluorescent staining with the VitroINK®?
- Is VitroINK® going to dry during the printing process?
- Does VitroINK® contain alginate?
- When preparing the mixture for printing, can I standardize the gelling times?
- What is the longest time the VitroINK® can be exposed to air and still be printed?
