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SPR Assay

 Biacore 8K can detect almost all biomolecules from various organic small molecules, peptides, proteins, nucleic acids, carbohydrates, lipids, phages, viruses and cells. Biacore 8K can also be used to study the interaction network composed of different molecules, complex assembly, protein conformational changes, thermodynamic parameters of molecular binding, and post-translational modifications of proteins. Biacore 8K provides high-quality analytical data, thereby effectively solving related problems in the current life science field.

  • Detection Indicator
    Biological specificity and selectivityCompound screeningConcentration analysisThe binding ability - affinity analysisTarget molecule activity Detection
    SPR Assay.webp
  • Wide Variety
    TGF-β superfamily (TGF-β1, TGF-β2, TGF-β3);Immunoglobulin Fc receptors (Fcγ RI, FCγ RIIB, FCγ RIIIA, FcRn from different species);Immunoglobulin superfamily cell adhesion molecules (Nectin-1, Nectin-2, Nectin-3, Nectin-4);Eph receptor family (EphA1, EphA2, EphA3, EphA4), insulin receptor (IR-A, IR-B, IGF1R), etc.
  • Fast Delivery
    Analysis data and reports will be issued within two weeks.
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What is preclinical testing?

In the process of  preclinical testing  of a compound or biological agent into a drug, the compound involved must go through the testing phase. First, we need to identify potential targets that can treat the disease. Then, a variety of compounds or preparations are screened out. Any compound that has shown potential as a drug for the treatment of this disease needs to be tested for toxicity before clinical testing to reduce the possibility of injury. preclinical testing What is the basis of preclinical testing? According to US Food and Drug Administration (FDA) regulations, a series of tests are required before a new drug is approved for use. In the first stage, basic research determines a hypothetical target for the treatment of a certain disease, and then screens small molecules or biological compounds to discover any substance with the potential to treat the disease. Then, a  preclinical research  phase followed, before which, as described above, the potential toxicity of the compou
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Inventory of the three major in vitro pharmacokinetic research methods

  The metabolic properties of a compound are an essential factor in whether or not it can be used as a drug in the clinical setting, so pharmacokinetic studies of newly synthesized compounds are required in drug development. In vitro incubation with liver microsomes, recombinant CYP450 enzyme lines, and in vitro incubation with hepatocytes are some of the more common in vitro drug metabolism methods. 1. In vitro incubation method with liver microsomes The metabolic stability and metabolic phenotypes of candidate compounds in different species of liver microsomes are good predictors of the metabolic properties of compounds in vivo. They are practical tools for evaluating candidate compounds in the pre-development phase of drug development. Liver microsomes include rat liver microsomes, human liver microsomes, canine liver microsomes, monkey liver microsomes, and mouse liver microsomes. In in vitro incubation of the liver, microsomes are the "gold standard" for in vitro d
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Novel Parkinson’s Therapies Possible with New Mouse Model

Parkinson's disease (PD) is a neurodegenerative disorder that is marked by the accumulation of the protein, α-synuclein (αS), into clumps known as Lewy bodies, which diminish neural health. Now, researchers from Brigham and Women's Hospital (BWH) report the development of a mouse model to induce PD-like αS aggregation, leading to resting tremor and abnormal movement control. The mouse responds to L-DOPA, similarly to patients with PD. The team's study (“Abrogating Native α-Synuclein Tetramers in Mice Causes a L-DOPA-Responsive Motor Syndrome Closely Resembling Parkinson’s Disease”) on the use of this transgenic mouse model appears in  Neuron . “α-Synuclein (αS) regulates vesicle exocytosis but forms insoluble deposits in PD. Developing disease-modifying therapies requires animal models that reproduce cardinal features of PD. We recently described a previously unrecognized physiological form of αS, α-helical tetramers, and showed that familial PD-causing missense mutati
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