Porcine CTX1 (Cross Linked C-telopeptide of Type 1 Collagen) Sandwich ELISA (STJE0006677)

SKU:
STJE0006677

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Applications: ELISA
Reactivity: Porcine
Note: FOR SCIENTIFIC EDUCATIONAL RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR OTHER MEDICAL APPLICATIONS.
Sensitivity: 0.188ng/mL
Detection Limit: 0.313~20ng/mL
Short Description: This CTX1 Sandwich ELISA is an in-vitro enzyme-linked immunosorbent assay for the measurement of samples in porcine cell culture supernatant, serum and plasma (EDTA, citrate, heparin).
Storage Instruction: If unopened the kit may be stored at 2-8°C for up to 1 month. If the kit will not be used within 1 month, store the components separately, according to the component table in the manual.
Assay Time: 3.5h
Detection: Colormetric
Specificity: This kit recognizes Porcine CTX 1 in samples. No significant cross-reactivity or interference between Porcine CTX 1 and analogues was observed.
Sample Type: Serum, plasma and other biological fluids
Background 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 Porcine CTXⅠ. Samples (or Standards) and biotinylated detection antibody specific for Human CLU are added to the micro ELISA plate wells. Human CLU would combined with the specific antibody. Then 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 Human CLU, 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 ± 2 nm. The OD value is proportional to the concentration of Porcine CTXⅠ. You can calculate the concentration of Human CLU in the samples by comparing the OD of the samples to the standard curve.

Information sourced from Uniprot.org

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