Rat TNF-β(Tumor Necrosis Factor Beta) ELISA Kit

Home / Products / Traditional ELISA / Rat ELISA Kits

Copy Product Information

Product No

FY-ER3820

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

DataSheet

说明书 MSDS

MSDS

Product Details

Product Name in English:

Rat TNF-β(Tumor Necrosis Factor Beta) ELISA Kit

Species:

Rat

Alternative Name:

LT, LTA, TNFB, TNFSF1, TNF Superfamily,Member 1, Lymphotoxin Alpha

Uniport ID:

Q06332

Assay Type:

Sandwich

Standard:

2000pg/mL

Sensitivity:

18.75 pg/mL

Detection Range:

31.25-2000pg/mL

Assay Time:

3.5H

Sample Type:

Serum, Plasma, Tissue homogenate and Other biological samples

Research:

Metabolic pathway;Neuro science;Developmental science;Nutrition metabolism;Bone metabolism;

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 TNF-β. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TNF-β. 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 TNF-β, 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 TNF-β 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
2000	2.309	2.327	2.318	2.284
1000	1.515	1.526	1.521	1.49
500	0.884	0.885	0.885	0.859
250	0.401	0.405	0.403	0.376
125	0.222	0.222	0.222	0.197
62.5	0.122	0.123	0.123	0.097
31.25	0.075	0.075	0.075	0.05
0	0.025	0.025	0.025	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)	83-97	90
EDTA plasma (n=8)	87-95	91
Cell culture media (n=8)	81-95	88

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 (%)	88-97	95-104	85-92
1:2	Average (%)	90	101	92
1:4	Range (%)	96-105	82-96	87-101
1:4	Average (%)	98	87	90
1:8	Range (%)	86-92	92-105	88-102
1:8	Average (%)	91	99	90
1:16	Range (%)	89-97	83-92	80-102
1:16	Average (%)	96	87	89

Assay Procedures

Related literature