Mouse C-P(C-Peptide) ELISA Kit (E-EL-M0354)
Add to cart
For research use only.
Product Summary
| Sensitivity | 0.1 ng/mL |
| Detection Range | 0.16-10 ng/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Mouse |
| Specificity | This kit recognizes Mouse C-P in samples. No significant cross-reactivity or interference between Mouse C-P and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, Tissue homogenate and Cell culture supernatant |
| Detection Method | Colorimetric method, ELISA, Sandwich |
| Assay Type | Sandwich-ELISA |
| Size | 96T / 48T / 24T / 96T*5 / 96T*10 |
| 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.
|
|||||||||||||||||||||||||||||||||||||||||||||
| Precision |
Intra-assay Precision (Within-run Precision): Three samples representing low, mid, and high concentrations of Mouse C-P were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Mouse C-P were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
|
|||||||||||||||||||||||||||||||||||||||||||||
| Recovery |
The recovery of Mouse C-P 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.
|
|||||||||||||||||||||||||||||||||||||||||||||
| Linearity |
Linearity of the assay was evaluated by spiking samples with high concentrations of Mouse C-P 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.
|
|||||||||||||||||||||||||||||||||||||||||||||
| 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.
|
|||||||||||||||||||||||||||||||||||||||||||||
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 Mouse C-P. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Mouse C-P 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 Mouse C-P, 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 ± 2 nm. The OD value is proportional to the concentration of Mouse C-P. You can calculate the concentration of Mouse C-P in the samples by comparing the OD of the samples to the standard curve.
Background
C-peptide (connecting peptide, C-P) is a 31-amino-acid peptide that links the A and B chains within proinsulin and is an intrinsic component of insulin biosynthesis. It is generated in pancreatic beta cells and cleaved from proinsulin by prohormone convertases within secretory granules, then released into the circulation in equimolar amounts with insulin. Because it directly reflects beta-cell secretory activity, C-peptide provides an index of endogenous insulin output.
C-peptide possesses anti-inflammatory, anti-apoptotic and microvascular-protective activities, improving endothelial function and tissue perfusion. Unlike insulin, it undergoes little hepatic first-pass clearance and has a longer half-life, and it is eliminated mainly by renal filtration, so it can also be measured in urine. Its slow clearance and equimolar secretion with insulin make it a stable and direct marker of residual beta-cell function.
Measurement of C-peptide is used to distinguish type 1 from type 2 diabetes, to assess residual beta-cell function in insulin-treated patients, to investigate the causes of hypoglycemia and to monitor graft status after islet transplantation. This ELISA kit enables sensitive and specific quantitative determination of C-peptide in serum, plasma and urine, serving diabetes research.
| Uniport ID | P01325 |
| Research Area | Metabolism , SignalTransduction |
-
IF:{{item.impact}}
Journal:{{item.journal}} ({{item.year}})
DOI:{{item.doi}}Reactivity:{{item.species}}
Sample Type:{{item.sample_type}}
-
Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}}
No files available. Please enter the correct identification code in the search area to query the relevant documents.
| Title | Status | Valid until | Action | |
|---|---|---|---|---|
| {{v.文件名}} | {{v.status_str}} | {{v.timestamp_str}} | Download | / |
*Note:Please download the relevant files within the validity period. After expiration, file preview and download will not be available on the page.
Resources
Contact with Us
Toll-free: 1-888-852-8623
Tel: 1-832-243-6086
Add:
14780 Memorial Drive, Suite 105, Houston, Texas, 77079, USA

