Human FAAH(Fatty-acid amide hydrolase) ELISA Kit

Home / Products / Traditional ELISA / Human ELISA Kits

Copy Product Information

Product No

FY-EH4273

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Assay Time

3.5H

Price($)

280 400

Size

48T 96T

Purchase details

Contact supplier to negotiate price details

100% Quality Assurance

Fast Shipping

Product Details

Product Name in English:

Human FAAH(Fatty-acid amide hydrolase) ELISA Kit

Species:

Human

Alternative Name:

Anandamide amidohydrolase 1,Anandamide amidohydrolase,FA2H,FAAH,FAAH-1,FAAH1,Fatty acid 2-hydroxylase,Fatty acid alpha-hydroxylase,Fatty acid amide hydrolase,Fatty-acid amide hydrolase 1,MGC12823,MGC138146,Oleamide hydrolase 1,Oleamide hydrolase

Uniport ID:

O00519

Assay Type:

Sandwich

Standard:

5000pg/mL

Sensitivity:

46.88 pg/mL

Detection Range:

78.13-5000pg/mL

Assay Time:

3.5H

Sample Type:

Serum, Plasma, Tissue homogenate and Other biological samples

Research:

Enzyme & Kinase;

Test Principle:

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to FAAH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to FAAH. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain FAAH, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of FAAH in the samples is then determined by comparing the OD of the samples to the standard curve.

Technical Data

As the OD values of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.

Concentration	OD1	OD2	Average OD	Corrected
5000	2.468	2.481	2.475	2.435
2500	1.612	1.619	1.616	1.579
1250	0.946	0.947	0.947	0.913
625	0.427	0.429	0.428	0.394
312.5	0.218	0.219	0.219	0.185
156.25	0.12	0.121	0.121	0.087
78.13	0.068	0.068	0.068	0.035
0	0.033	0.033	0.033	0

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level were tested on 3 different plates, 20 replicates in each plate, respectively.

Item	Intra-assay Precision	Intra-assay Precision
Sample	3	3
Replicate	9	18
CV(%)	5	8

Rate of recovery

The recovery of spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.

Sample Type	Range(%)	Average Recovery(%)
Serum (n=8)	93-107	100
EDTA plasma (n=8)	87-99	93
Cell culture media (n=8)	87-95	91

Linear

Samples were spiked with high concentrations of target proteins and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.

		Serum (n=5)	EDTA plasma (n=5)	Cell culture media (n=5)
1:2	Range (%)	83-98	89-97	85-99
1:2	Average (%)	92	92	91
1:4	Range (%)	88-97	89-97	80-93
1:4	Average (%)	92	90	81
1:8	Range (%)	96-105	85-94	89-97
1:8	Average (%)	102	93	95
1:16	Range (%)	86-92	80-96	85-94
1:16	Average (%)	89	92	88

Assay Procedures

Related literature