Researchers take advantage of MBL International’s recombinant IL-18 to activate varying cells like peripheral blood cells, macrophages, NK cells and T cells to identify targets.
Explore the Limitless Potential of IL-18
Caspase Activity: Essential for Apoptosis
MBLI ‘s APOPCYTO Caspase-3,8,9 Colorimetric Assay Kit detects caspase activity in cell extract with LEHD-pNA as a substrate, in which LEHD sequence is recognised by each active caspase selectively.
Why should you use Isotype Control Antibodies – MBL
Isotype control antibodies optimise study performance & data analysis in therapeutic antibody research, which is key to drug development.
Ensure Accurate Immune Monitoring Results with Negative Controls
Negative controls aid precision of immune response monitoring. For HLA-A*02:01 alleles, MBLI offers a “Negative Tetramer” in BV421, PE or APC.
Visualising Protein-Protein Interaction with FLUOPPI Technology
MBLI’s innovative technology, Fluoppi, simplifies the visualisation of protein-protein interaction.
Validation of Neoantigen In Silico Prediction using QuickSwitch™ Kits
Research findings indicate that neoantigens have the potential to activate tumour-specific T-cell-mediated anti-tumour immune responses.
Therapeutic Targets of the NAD+ Biosynthesis Pathway
CycLex NAMPT Colorimetric Assay Kit detects nicotinamide phosphoribosyltransferase (NAMPT) activity in recombinant NAMPT or endogenous NAMPT immunoprecipitated from cell extract.
Discover the Ab-Match ELISA Series: Unveiling Cancer Biomarkers and Beyond
The Ab-Match series by MBL are innovative ELISA kits for the detection of cancer antigens. These convenient kits come with all the necessary components for successful detection.
Tetramer Gating Strategy For True Positives Results
Investigators have developed a gating strategy that effectively minimises non-specific staining by incorporating a dump channel.
Histone deacetylase (HDAC): important consideration in regulating gene expression
Histone deacetylase (HDAC) plays a pivotal role in the regulation of gene expression through the modification of nucleosome structure.