Rat CD48 (Cluster Of Differentiation 48) ELISA Kit (E-EL-R3080)
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For research use only.
Product Summary
| Sensitivity | 46.88 pg/mL |
| Detection Range | 78.13-5000 pg/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Rat |
| Specificity | This kit recognizes Rat CD48 in samples.No significant cross-reactivity or interference between and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, plasma and other biological fluids |
| Detection Method | Colorimetric method, ELISA, Sandwich |
| Assay Type | Sandwich-ELISA |
| Size | 96T / 48T / 24T / 96T*5 |
| Storage | 2-8℃ |
| Expiration Date | 12 months |
Performance
| Typical data |
The following data was generated by the Quality Control Department, under controlled laboratory conditions (ambient temperature: 18-25 °C, relative humidity: 35-75%) using standardized procedures (TMB reaction at 37 °C in the dark for 15 minutes, followed by termination and OD measurement). These values are provided for reference only.
Actual results may vary due to differences in laboratory conditions, operator technique, and equipment. Users are required to generate a standard curve using their own experimental data.
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| Precision |
Intra-assay Precision (Within-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Rat CD48 was evaluated by spiking samples at low, mid, and high concentrations across the assay range in various sample matrices.
The assay performance was assessed by comparing the measured concentrations to the expected spiked amounts to determine the percent recovery.
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| Linearity |
Linearity of the assay was evaluated by spiking samples with high concentrations of Rat CD48 and performing serial dilutions using Standard & Sample Diluent to produce concentrations spanning the assay's dynamic range.
The measured values were then compared to the expected concentrations to assess the linearity of response.
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| Stability |
Each kit batch is subjected to accelerated stability testing and real-time stability monitoring. Sample performance is evaluated after storage at 37 °C for 10 days to assess the impact of elevated temperature on assay reliability and reagent integrity.
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Test Principle
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 Rat CD48. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat CD48 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Rat CD48, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 9 nm. The OD value is proportional to the concentration of Rat CD48. You can calculate the concentration of Rat CD48 in the samples by comparing the OD of the samples to the standard curve.
Background
CD48 protein is a glycosylphosphatidylinositol (GPI)-anchored cell surface protein belonging to the CD2 subfamily of the immunoglobulin superfamily (IgSF). Its basic functions include acting as an adhesion molecule and co-stimulatory molecule, participating in the adhesion, activation, and signal transduction of immune cells by binding to ligands such as CD2, CD244 (2B4), and bacterial component FimH.Structurally, CD48 consists of a signal peptide, two immunoglobulin-like variable regions (IgV), and two constant regions (IgC2), without a transmembrane domain. Instead, it is fixed to the cell membrane through a GPI anchor structure at the C-terminus. This structure enables it to interact with Src family kinase Lck through lipid raft regions, thereby triggering tyrosine phosphorylation and related signaling pathways.CD48 is expressed on the surface of various immune cells, including T cells, B cells, natural killer cells (NK cells), dendritic cells (DCs), and mast cells, and its expression is regulated by multiple factors such as viral and bacterial products as well as inflammatory cytokines. By binding to ligands, CD48 can activate Lck kinase, promote TCR signaling, enhance T cell activation, and regulate effector functions in NK cells and CTLs.CD48 also has significant clinical implications, such as serving as a target for immunotherapy in the treatment research of multiple myeloma and other cancers.
| Gene Alias | Cd48 |
| Gene ID | 245962 |
| Uniport ID | P10252 |
| Protein Alias | Cd48 |
| Research Area | Immunology , SignalTransduction |
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