Intended use
This ELISA kit is intended for use in quantitating Trypsin, recombinant from porcine pancreas. The kit is for research use only and is not intended for diagnostic use in human or animals.
Principle of the Procedure
This Trypsin assay is a two-site immunoenzymtric assay. The recombinant trypsin from porcine pancreas, expressed in E.Coli, from YAXINBIO, in the samples are reacted in microtiter wells coated with a purified capture antibody. An anti-trypsin monoclonal antibody conjugated with the enzyme horseradish peroxidase (HRP) is reacted simultaneously forming a sandwich complex of solid phase antibody-trypsin-HRP labeled antibody. After a wash step to remove any unbound reactants, the wells are then reacted with tetramethylbenzidine (TMB) substrate. The amount of hydrolyzed substrate is read on a microtiter plate reader and will be directly proportional to the concentration of recombinant trypsin present in the samples. Accurate quantitation is achieved by comparing the signal of recombinant trypsin standards assayed at the same time.
Reagents & Materials Provided
Vial cap | Label | Contents | Storage |
Anti-trypsin Coated plate Dismountable Micro ELISA Plate in a sealed bag | 8 wells×12 Strips | -20°C | |
A1 | Trypsin Standard (lyophilizates) | 4×10 ng | 2-8°C |
A2 (250×) | HRP Conjugated Anti-trypsin Concentrate Mouse monoclonal Antibody to recombinant trypsin conjugated with HRP in a protein matrix with preservatives | 1×0.05 mL | -20°C |
P1 | Diluent Concentrate (25×) For Standard, Samples & HRP-Ab | 1×5 mL | 2-8°C |
P2 | Wash Concentrate (25×) | 1×40 mL | 2-8°C |
A3 | TMB-Substrate 3,3’,5,5Tetramethylbenzidine | 5×0.125 mL | -20°C Avoid Light |
P3 | TMB Diluent (Substrate Reagent) | 1×15 mL | 2-8°C Avoid Light |
P4 | Stop Solution | 1×5 mL | 2-8°C |
Plate Sealer (Reuseable) | 5 sheets | ||
Product insert | 1 | ||
Certificate of Analysis | 1 |
Materials & Equipment Required But Not Provided
Microtiter plate reader spectrophotometer with dual wave length capability at 450 & 650 nm. If your plate reader does not provide dual wave length analysis, you may read at just the 450 nm wave length.
Pipettors – 50 μL and 100 μL
Repeating or multichannel pipette – 100 μL
Incubator, 37°C
Clean absorbent pad
Precautions
It is not intended for diagnostic use in human or animals.
Stop reagent is 0.5M H2SO4. Avoid contact with eyes, skin and clothing. At the concentrations used in this kit, none of the other reagents are believed to be harmful.
This kit should only be used by qualified technicians.
Performance Characteristics
YAXINBIO has validated the assay by conventional criteria as indicated below.
Sensitivity
The lower limit of detection (LOD) is defined as that concentration corresponding to a signal two standard deviations above the mean of the zero standard. LOD is ~11 pg/mL in the recommended protocol. The lower limit of quantitation (LOQ) is defined as the lowest concentration, where concentration coefficients of variation (CVs) are <20%. The LOQ is ~156 pg/mL.
Precision
Precision is defined as the percent coefficient of variation (%CV). This is calculated by dividing the standard deviation by the mean value for a number of replicate determinations of two different control samples in the low and high concentration range of the assay. Both intra-assay and inter-assay precision were determined on 2 pools with low (~1.25 ng/mL) and high concentrations (~10 ng/mL).
Intra-assay
Number of Test | X (ng/ml) | % CV |
20 | 1.25 | 6.3 |
20 | 10 | 3.2 |
Inter-assay
Number of Assays | X (ng/ml) | % CV |
8 | 1.25 | 7.6 |
8 | 10 | 4.6 |
Specificity/Cross-Reactivity
This ELISA kit is intended to detect Trypsin, recombinant from porcine pancreas. It is suggested that the compatibility of the kit calibration be conducted, if it is used for other type of trypsin.
The following materials were tested for cross reactivity at the concentrations indicated both in the absence of recombinant trypsin and in the presence of 5 ng/mL recombinant trypsin. None of these materials were found to yield any statistically significant false increase or decrease in apparent recombinant trypsin concentrations. It is recommended that each user test known materials in their sample matrices for cross reactivity in a similar experiment, when it is necessary.
Materials not cross reactive for recombinant trypsin
Substances | Concentration tested |
human plasma | Undiluted |
human serum | Undiluted |
LB medium | Undiluted |
Recombinant carboxypeptidase B expressed in E.Coli | 1 mg/ml |
Limitations
Trypsin from other suppliers other than YAXINBIO may show a different reactivity with regard to sensitivity and accuracy. Therefore the compatibility of the kit calibration to the individual trypsin product must be verified.
Matrix interference
Although the assay is designed to minimize matrix interference, certain sample matrices may interfere in this assay. Materials, such as detergents and salt in high concentration, extremes of pH (<6.0 and >8.5) or very high protein concentrations may give erroneous results. It is recommended to test the sample matrix for interference by diluting the 10 ng/mL standard to analyze the recovery.
Hook Capacity
High Dose Hook Effect may be observed in samples
with very high concentrations of recombinant trypsin. The readings of samples greater than 10 ng/mL (80ng,100ng,500ug,1mg/mL) may give absorbencies less than the 40ng/mL standard. It is highly recommended that samples should be assayed by diluted, when their readings were ≧10 ng/ml.
Quality Control
Precision on duplicate samples should yield average coefficients of variation of less than 10% for samples greater than 1 ng/mL. CVs for samples <1 ng/mL may be greater than 10%. It is recommended that each laboratory assay appropriate quality control samples in each run to insure that all reagents and procedures are correct.
Assay Time
Incubation time: 1 h 45 min to 2 hours
Total assay time: approximately 2 to 2.5 hours
Notes for samples
Samples should be assayed within 7 days, when stored at 4°C, or divided and stored at -20°C (≤1 month) or -80°C (≤3 months). Avoid repeated freeze-thaw cycles.
The supernatants, centrifuged of