The Human SELE (E-Selectin) Quickstep ELISA Kit is designed for the quantitative detection of Human SELE (E-Selectin) levels in various biological samples. E-Selectin is a biologically active molecule with established roles in cancer, metabolism, neuroscience pathways. It participates in key cellular and molecular processes that regulate physiological homeostasis, and dysregulation of its expression or activity has been associated with pathological states across multiple disease contexts. The precise quantification of Human E-Selectin in biological samples is critical for elucidating its mechanistic contributions to disease pathogenesis, identifying clinically relevant biomarker associations, and supporting the development of novel diagnostic tools and targeted therapeutic interventions. Assay Genie's Human SELE (E-Selectin) Quickstep ELISA Kit offers exceptional sensitivity and specificity with a sensitivity of 75.01 pg/mL, ensuring reliable and reproducible results across a broad range of sample types including serum, plasma and other biological fluids. Manufactured under stringent quality control standards, this ELISA kit provides robust performance and ease of use, making it an outstanding choice for both research and clinical applications. Trust Assay Genie's Human SELE (E-Selectin) Quickstep ELISA Kit for accurate and dependable quantification of this crucial biomarker in your studies.
Product Name:
Human SELE (E-Selectin) Quickstep ELISA Kit
SKU:
QSES092
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
1 h 30 min
Sensitivity:
75.01 pg/mL
Detection range:
125-8000 pg/mL
Reovery:
80%-120%
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to the target protein. Standards or samples are added to the micro ELISA plate wells and bind to the immobilized antibody. A biotinylated detection antibody specific to the target protein is then added, followed by Avidin-Horseradish Peroxidase (HRP) conjugate. Free components are washed away. The substrate solution is added to each well, resulting in a color change. Only wells containing the target protein, detection antibody, and HRP conjugate will develop a blue color. The reaction is terminated by the addition of stop solution, resulting in a yellow color. The optical density (OD) is measured at 450 nm ± 2 nm. The OD value is directly proportional to the concentration of the target protein in the sample and is determined using a standard curve.
