Last Chance Human Cc2d1a(coiled Coil And C2 Domain Containing Protein 1a) Elisa Kit In Multiple Colors [IFON0t9P]
Human CC2D1A ELISA Kit: Precision and Simplicity in Protein AnalysisIntroducing the Last Chance Human Cc2d1a(coiled Coil And C2 Domain Containing Protein 1a) Elisa Kit In Multiple Colors [IFON0t9P], a state-of-the-art diagnostic tool designed for accurate and efficient protein analysis. This
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Human CC2D1A ELISA Kit: Precision and Simplicity in Protein Analysis
Introducing the Last Chance Human Cc2d1a(coiled Coil And C2 Domain Containing Protein 1a) Elisa Kit In Multiple Colors [IFON0t9P], a state-of-the-art diagnostic tool designed for accurate and efficient protein analysis. This kit offers a streamlined approach to detecting and quantifying CC2D1A protein levels in biological samples, making it an invaluable asset in research and clinical diagnostics. With its robust design and user-friendly protocol, this kit ensures reliable results every time.- High specificity for CC2D1A, minimizing cross-reactivity and false positives.
- Optimized protocol for ease of use and rapid results, saving valuable time and resources.
- Comprehensive kit contents, including all necessary reagents and buffers.
Product Specifications and Technical Details
The Human CC2D1A ELISA Kit is meticulously designed to meet the highest standards of quality and accuracy. This kit utilizes a sandwich enzyme-linked immunosorbent assay (ELISA) technique, which provides a sensitive and reliable method for measuring protein levels. Key specifications include:- Assay format: 96-well microplate
- Assay sensitivity: 0.78 pg/mL
- Dynamic range: 0.78 pg/mL to 50 pg/mL
- Incubation time: 1 hour
- Kit shelf life: 12 months from the date of manufacture
Applications and Benefits of the Human CC2D1A ELISA Kit
The Human CC2D1A ELISA Kit is a versatile tool with wide-ranging applications in both research and clinical settings. Its precision and sensitivity make it ideal for:- Research on CC2D1A expression in various diseases, including cancer and neurodegenerative disorders.
- Monitoring therapeutic interventions targeting CC2D1A in clinical trials.
- Diagnosis of genetic disorders associated with CC2D1A mutations.
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