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Next Generation Albumin

With the development of science and technology, a lot of studies are being performed to bioengineer next-generation albumins to enhance the curative effects of albumin. The key point of the new technology is the manipulation of the FcRn and albumin complex, which required albumin variants that have longer and shorter half-lives than natural albumin. To this end, scientists have used a structure-based approach, supported by the analysis of site-specific mutants, to identify residues involved in the binding of albumin to FcRn. Results show that both FcRn and albumin domain III in this complex allow specific molecular interactions. The development of the FcRn-albumin complex may speed up the process of novel albumin variants with altered serum half-life as carriers of drugs.

Quantification of Ribosomal Proteins

The quantification of ribosomal proteins in biological samples has been routinely used for the diagnosis of diseases and monitoring the treatment. However, large-scale protein quantification in complex samples is still a challenging task, while ribosomal proteomics attracts more attention. In addition to their canonical ribosomal functions, multiple ribosomal proteins have extra-ribosomal functions resulting in cell cycle arrest and apoptosis. Defects in ribosome biogenesis, translation, and the functions of individual ribosomal proteins, including mutations in ribosomal proteins, have been linked to a diverse range of human congenital disorders termed ribosomopathies.

The 6-azauridine

Single Cell Omics Solutions

Tumor-infiltrating immune cells have been regarded as attractive markers for revealing immune responses and tumor control in various cancer immunotherapies. Single cell omics for immunity technologies have been widely used for analyzing the heterogeneity of cells and molecules in the tumor microenvironment (TME). Meanwhile, scOmics analysis of tumor-infiltrating immune cells is also critical to determining cell interactions in cancer research. Single Cell now offers a collection of single-cell omics services for quantifying different cell types, such as T cells, B cells, dendritic cells (DCs), natural killer cells (NKs), macrophages, myeloid-derived suppressor cells (MDSCs), and neutrophils.

Whole Transcriptome Sequencing Service for Cancer

RNA services for cancer are important for interpreting the functional elements of the genome as well as for understanding the underlying mechanisms of diverse diseases, especially cancers. Microarray-based gene expression approaches have been used for high-throughput, large-scale RNA-level studies, such as to identify differentially expressed genes. However, the application of microarray technologies has been limited by their hybridization-based nature. Advances in massively parallel DNA sequencing technologies have enabled RNA-seq by sequencing cDNA.

CD16 EGFR scIgG

Recombinant Anti-CD16 EGFR scIgG is designed to be expressed as two chains; each chain has the same units as their parental IgG antibodies, anti-CD16 and anti-EGFR IgGs. The two chains form heterodimers via Fc KIH technology. This BsAb can retarget NK cells toward tumor cells. It is designed for the research of Head and neck cancer, Colorectal cancer (CRC), Glioblastoma multiforme (GBM), Squamous cancer, glioblastoma, medulloblastoma, Non-small cell lung cancer (NSCLC), Renal cell cancer (RCC), and solid tumor therapy.

Stable Cell Line Service

Stable cell lines are suitable not only for manufacturing therapeutic and diagnostic antibodies but also for drug screening and applications in pharmacological and toxicological studies. At Creative Biolabs, we provide cGMP-compliant stem cell banking in strict accordance with industry standards to ensure that our customers have access to fully characterized and phenotypically consistent cells. Together with our antibody production services, the master cell bank (MCB) and working cell bank (WCB) we offer can be used for routine laboratory use or therapeutic antibody generation.