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Unser breites Angebot enthält Multiplex-Panels, für die Sie die Analyten auswählen können, die am besten für Ihre Anwendung geeignet sind. Unter einem separaten Register können Sie das Premixed-Cytokin-Format oder ein Singleplex-Kit wählen.
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Die folgenden MAPmates™ sollten nicht zusammen analysiert werden: -MAPmates™, die einen unterschiedlichen Assaypuffer erfordern. -Phosphospezifische und MAPmate™ Gesamtkombinationen wie Gesamt-GSK3β und Gesamt-GSK3β (Ser 9). -PanTyr und locusspezifische MAPmates™, z.B. Phospho-EGF-Rezeptor und Phospho-STAT1 (Tyr701). -Mehr als 1 Phospho-MAPmate™ für ein einziges Target (Akt, STAT3). -GAPDH und β-Tubulin können nicht mit Kits oder MAPmates™, die panTyr enthalten, analysiert werden.
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48-602MAG
Buffer Detection Kit for Magnetic Beads
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03-0175-00
MilliporeSMC™ Immunogenicity Bead Based Assay Development Kit
SMC™ technology enables ADA assay development by labelling the drug with capture & detection reagents and utilizing buffer reagents for optimization. It allows you to develop a homogenous species-independent assay format that is simple, easy to design and validate.
More>>SMC™ technology enables ADA assay development by labelling the drug with capture & detection reagents and utilizing buffer reagents for optimization. It allows you to develop a homogenous species-independent assay format that is simple, easy to design and validate. Less<<
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Übersicht
Replacement Information
Description
Catalogue Number
03-0175-00
Trade Name
SMC™
Description
SMC™ Immunogenicity Bead Based Assay Development Kit
Overview
All biological therapeutics have the potential to induce an immune mediated response ranging from benign to severe adverse effects. These effects can encompass diminished clinical efficacy of the biotherapeutic being administered to hypersensitivity, allergic reaction or even cytokine storms. Consequently, regulatory agencies are looking to understand the implications of immunogenicity and are directing the industry to integrate programs for immunogenicity risk management starting in early phase drug development in clinical and pre-clinical.
Traditionally ELISAs or Electrochemiluminescence (ECL) have been used to identify the presence of anti-drug antibodies (ADA). Though effective for detection, ELISA methods often fail to adequately measure specific antibody response in the presence of circulating protein therapeutic due to the limitation on sensitivity and problems presented on a plate-based format.
According to FDA Guidance (2019), ADA assays should be sufficiently sensitive to detect low levels of ADA before the amount of ADA impact the PK, PD, safety or efficacy.
Single Molecule Counting (SMC™) technology, a fluorescent based immunoassay technique, not only offers a magnitude fold increase in sensitivity over current existing technologies, it also enables the development and optimization of homogenous, species-independent ADA assays.
Combining our Immunoassay portfolio to study the impact on the immunogenicity of a therapeutic can provide great insight into the mechanism of the response. The SMC™ technology can offer increased sensitivity which may assist in the detection of low affinity antibodies and lead to earlier detection of primary ADA response, overcome matrix effects and may reduce drug tolerance. Our MILLIPLEX® kits can offer insight into the mechanism of the response and also help understand the immune complex mediated responses to the ADA. Related products include the high senstivity T cell panels (HSTCMAG-28SK, MHSTCMAG-70K), the complement panels (HCMP1MAG-19K, HCMP2MAG-19K), and the immunoglobulin isotyping panels (HGAMMAG-301K, HGAMMAG-303E, MGAMMAG-300K, MGAMMAG-300E).
Background Information
SMC™ technology enables the development of ADA assays by the labelling of the drug with capture & detection reagents, and utilization of buffer reagents to develop and optimize the assays. The technology allows the ability to develop a homogenous species-independent assay format that is simple, easy to design and validate. The reduced number of wash steps aids in the detection of low affinity antibodies and decreases assay time. This assay format is often referred to as a “bridging assay” since the ADA acts as a bridge between the drug labelled capture & detection.
References
Product Information
Components
Capture Label
Detection Label
Buffer 1
Buffer 2
Buffer 3 (10X)
Filter Tube Ultrafree Ultracel-20 membrane
10X Wash Buffer
Coated Bead Buffer
Uncoated SMC Beads
Discovery Standard Diluent
Elution Buffer B
Buffer D
10X Systems/Wash Buffer w/ Proclin
Applications
Application
SMC™ technology enables ADA assay development by labelling the drug with capture & detection reagents and utilizing buffer reagents for optimization. It allows you to develop a homogenous species-independent assay format that is simple, easy to design and validate.
Key Applications
Single Molecule Counting (SMC™)
Application Notes
In developing an immunogenicity assay, optimization is required to fully validate for the immunological system being studied. Considerations such as those listed below can be easily studied with the SMC technology platform: • Drug tolerance • Cut point/Matrix Tolerance • Sensitivity/Dynamic range of the assay • Reproducibility • Reagents suitable for up to approximately 30 bead-based assays.
Biological Information
Physicochemical Information
Sensitivity
Further optimization of different variables can take place to produce the most sensitive assay. These include: ◦Drug concentration (capture and detection reagent) ◦Assay diluents (to mitigate HAMA or other interfering factors) ◦Sample volume ◦Number of wash steps ◦Incubation time ◦Standard / sample diluent ◦Determination of minimum required dilution (MRD) ◦Evaluation of drug interference / tolerance
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Usage Statement
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.