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Xenograft
- Is VitroGel® biocompatible for in vivo study?
- Can I use VitroGel® for in vivo studies? What is the injectability of VitroGel®?
- What is the injection volume of VitroGel®?
- What is the recommended number of cells for VitroGel® injection?
- 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?
- Do I have to add serum, growth factors, or supplements to the cell suspension before mixing with VitroGel®?
- If I want to add supplements to boost cell growth, what are the common growth factors or components used?
- Does adding serum and other cytokines at a high concentration to the cell suspension before mixing with VitroGel® lead to bubble formation?
- Can VitroGel® be used for injection in mice at different sites?
- What is the tumor formation rate and growth kinetic in VitroGel®?
- Are there data on the successful cell types that have worked with VitroGel®, specifically for xenograft?
- What type of needles can you use for animal injection?
- When the mixture of the cells and the VitroGel® is left to stabilize at room temperature before the injection, will the suspension cells sink to the bottom of the tube?
- How can I decide the mixing ratio between ready-to-use hydrogel solution and cell suspension while preparing samples for xenograft application?
- How to counter ulceration problem if seen at tumor site?
- Can VitroGel® be injected anywhere in the animal or are there any limitations for some organs, for example, brain, lungs, etc?
- How can I improve tumor size or weight?