AMSBIO Product Update

Proliferation of transplanted colorectal cancer cells (red) and stroma tissue (green) in MatriMix for PDX

MatriMix for PDX - perfect for personalized medicine and drug screening.

Optimized for PDX models: MatriMix is designed to preserve native tumor architecture and microenvironment, enhancing the viability of patient-derived tumor cells.
Ready to use: Single vial formulation
Consistent and reproducible composition: Manufactured with high purity and minimal batch-to-batch variability.
Enhanced imaging and analysis: MatriMix is a clear gel at 37°C, allowing for superior imaging possibilities (e.g. microscopy).

Liver cancer spheroid stained using CellO-IF technology.

Streamlined Workflows: Reduced number of reagents and steps.
Effortless Labelling: Label organoids, spheroids, and cells while still in hydrogel and extracellular matrix.
Enhanced Clarity: Reduces background noise for high-resolution images.
Optimize Detection: Boosted antigenicity for clearer visualization of targets.

As featured in Genetic Engineering News and more!

Need to plate bacterial and yeast cells on agar plates? Try our EZ-spread™ plating beads!

Fast, uniform cell distribution: Sterile, precision-molded beads ensure even spreading in seconds, enhancing colony formation.
Safe and Convenient: Eliminate the need for glass rods and hazardous ethanol flaming.
Ready-to-Use Packaging: Pre-sterilized in dispenser bottles for 100 plates or single-use tubes for 50 plates.

Ease of automation with minimal accessory requirements
Compatibility with platforms like KingFisher®, Hamilton®, and TECAN®
Industry-leading mechanical stability for reliable results
A MagSi-STA Trial Kit to evaluate the best bead specification for your workflow.
Proven for downstream applications such as PCR and NGS library prep

Looking for reliable tumor tissues for your research?

Complete NGS sequencing data available, including chromosomal position, variant type (SNP or indel), alternate allele variations, quality score, depth of coverage, allele type, transcript ID and more.
Includes comprehensive clinical history when available.
Ideal for verification, genotyping, or identification of new mutations.
Suitable for both IHC and in-situ hybridization assays

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