|The Human NOS1 n/a (Catalog #MBS2000845) is a CLIA Kit and is intended for research purposes only. The product is available for immediate purchase. The MBS2000845 CLIA Kit recognizes Human (General) NOS1.
To buy or view more detailed product information and pricing, please click on the technical datasheet page below:
(Or you can also download the PDF Manual
for complete product instructions).
Please refer to the product datasheet for known applications of a given clia kit. We\'ve tested the Nitric Oxide Synthase 1, Neuronal (NOS1) CLIA Kit with the following immunoassay(s):
Typical Testing Data/Standard Curve (for reference only)
Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated secondary antibody. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate An and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Nitric Oxide Synthase 1, Neuronal (NOS1) level in the sample or standard.
Samples: Serum, plasma, tissue homogenates and other biological fluids
Detection Range: 13.72-10000pg/mL
Sensitivity: The minimum detectable dose of this kit is typically less than 6.03pg/mL. Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Nitric Oxide Synthase 1, Neuronal (NOS1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Nitric Oxide Synthase 1, Neuronal (NOS1) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Assay Procedure Summary: 1. Prepare all reagents, samples and standards;
2. Add 100uL standard or sample to each well. Incubate 2 hours at 37 degree C;
3. Aspirate and add 100uL prepared Detection Reagent A. Incubate 1 hour at 37 degree C;
4. Aspirate and wash 3 times;
5. Add 100uL prepared Detection Reagent B. Incubate 30 minutes at 37 degree C;
6. Aspirate and wash 5 times;
7. Add 100uL Substrate Solution. Incubate 10 minutes at 37 degree C;
8. Read RLU value immediately.