Chimeric Antigen Receptor T (CAR-T) are T cells that are genetically engineered and are used in cell therapy. Our expert team of scientists is committed to provide a wide range of services in CAR-T cell therapy research. T-cell cytotoxicity assay Target cells (tumor cells) loaded with CFSE, co-incubated with effector cells 7-AAD added to quantify compromised cells FACS analysis CD107a degranulation assay (optional) Immune-cell profiling Isolation and enrichment of immune cell subsets Characterization of immune-oncological agents using FACS Cytokines release – multiplex cytokine analysis using ELISA Treg-immune suppression assay Human CD4+CD25+ Treg will be isolated using kit (miltenyibiotec) Will be co-cultured with respondent (Tresp) cells FACs analysis will be to check in vitro suppression of Tresp cells Other assays Antibody Dependent Cell Mediated Cytotoxicity (ADCC) assay Complement Dependent Cytotoxicity (CDC) assay Antibody Dependent Cellular Phagocytosis (ADCP) FACS based NK-mediated cell killing assay T-cell receptor sequencing for biomarker identification
Pre-clinical proof of concept
In vitro and In vivo models for screening and efficacy
Experience in multiple assays
Strong framework data recording and traceability
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Aurigene Pharmaceutical Services is a leader in the synthesis of activated MethoxyPolyethyleneGlycol(m-PEGs), With a comprehensive product range and customized services. ...
Read More2020
A novel approach for the spiro-isoindolinone dihydroquinazolinones has been demonstrated from 2- aminobenzamide and 2-cyanomethyl benzoate in the presence of KHMDS as a base to get moderate yields. The reaction has been screened in various bases followed by solvents and a gram scale reaction has also been executed under the given conditions. Based on the controll...
Read More2005
An improved and rapid synthesis of mefenamic acid based indole derivatives has been achieved via the ligand free Cu-catalyzed coupling-cyclization method under ultrasound irradiation. This simple, straightforward and inexpensive one-pot method involved the reaction of a terminal alkyne derived from mefenamic acid with 2- iodosulfanilides in the presence of CuI ...
Read More2005
The formal synthesis of Cladospolide-C and its analog is achieved by using enantiopure (R)-g evalerolactone 10. The significant points of this synthesis are the stereoselective dihydroxylation of a, bunsaturated ester 16 using Sharpless protocol, Wittig olefination of g evalerolactol 6 with triphenylphosphonium iodide salt 7, one pot selective oxidation ...
Read More2005
A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a catalyst, giving good to moderate yields. In this reaction the substrate scope for amines and aldehydes was also investigated. The reaction has been checked on a large scale ...
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