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Canine CRP (C-Reactive Protein) ELISA Kit (E-EL-C0243)

Canine CRP (C-Reactive Protein) ELISA Kit - 1
  • Canine CRP (C-Reactive Protein) ELISA Kit - 1
  • Canine CRP (C-Reactive Protein) ELISA Kit - 2
  • Canine CRP (C-Reactive Protein) ELISA Kit - 3
All Size Price Qty
96T $ 609.00
- +
48T $ 487.00
- +
24T $ 150.00
- +
96T*5 Inquire /
96T*10 Inquire /
Add to cart

For research use only.

Product Summary
Sensitivity 0.94 ng/mL
Detection Range 1.56-100 pg/mL
Sample Volume 100 μL
Total Assay Time 3 h 30 min
Reactivity Canine
Specificity This kit recognizes Canine CRP in samples.No significant cross-reactivity or interference between Canine CRP 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 / 96T*10
Storage 2-8℃
Expiration Date 12 months
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.
pg/mL OD1 OD2 Mean OD Corrected OD
100 2.146 2.112 2.129 2.054
50 1.701 1.683 1.692 1.617
25 0.976 0.944 0.960 0.885
12.5 0.480 0.480 0.480 0.405
6.25 0.269 0.275 0.272 0.197
3.13 0.177 0.171 0.174 0.099
1.56 0.131 0.121 0.126 0.051
0 0.074 0.076 0.075 -
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.
/ Intra-assay Precision Inter-assay Precision
Sample 1 2 3 1 2 3
Numbers 20 20 20 20 20 20
Mean(pg/mL) 4.960 12.420 49.400 5.200 12.630 53.140
Standard deviation 0.330 0.500 2.240 0.350 0.840 3.380
CV(%) 6.590 4.060 4.540 6.790 6.670 6.360
Recovery
The recovery of Canine CRP 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.
Sample Type Range (%) Average Recovery(%)
Cell culture media (n=8) 88-101 94
Serum (n=8) 90-106 97
EDTA plasma (n=8) 89-103 95
Linearity
Linearity of the assay was evaluated by spiking samples with high concentrations of Canine CRP 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.
/ / Cell culture media
(n=5)
EDTA plasma
(n=5)
Serum
(n=5)
1:2 Range 98-112 97-111 96-113
Average 95 103 91
1:4 Range 87-102 88-101 95-106
Average 101 87 98
1:8 Range 82-98 82-97 86-99
Average 98 101 101
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.
/ Variation range of 37°C mean
concentration / 2-8°C mean
Sample 1(n=16) 92.43-113.79
Sample 2(n=16) 94.14-95.73
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 ApoH . 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 ApoH 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 ApoH , 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 Rat ApoH . You can calculate the concentration of Rat ApoH in the samples by comparing the OD of the samples to the standard curve.
Apolipoprotein H (ApoH), also known as beta 2‑Glycoprotein I/ beta 2-GPI, is a variably glycosylated member of the complement control superfamily of proteins with a molecular weight of aproximately 33 kDa . ApoH also associates with liposomes and apoptotic cell debris, thereby enabling their renal clearance via Megalin uptake. Circulating levels of ApoH are postively correlated with triglyceride-rich lipoprotein (VLDL) components in type II diabetes. ApoH inhibits thrombosis by blocking the activation of Coagulation Factor XI but also shows procoagulant activity by inhibiting the activation of Protein C . ApoH can be cleaved by Plasmin at Lys317‑Thr318, an action that is enhanced by heparin. ApoH cleavage reduces its ability to bind phospholipids and inhibit Factor XI activation but confers the ability to bind Plasminogen. Cleaved ApoH also demonstrates antiangiogenic activity, whereas intact ApoH does not (14). The production of antibodies against ApoH is a hallmark of Antiphospholipid Syndrome (APS), an autoimmune disorder that leads to hypercoagulability and recurrent miscarriages. ApoH binds to the surface antigen of Hepatitis B Virus and is associated with the development of HBV-induced hepatocellular carcinoma.
Uniport ID T2KEN6
Research Area Cancer , Cardiovascular
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