Rat ELISA Kits

Home / Products / Traditional ELISA / Rat ELISA Kits
Rat βTG/PBP/CXCL7/NAP2(Thromboglobulin, Beta) ELISA Kit
Copy Product Information

Product No

FY-ER5641

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

Manual(EN) Manual(EN) Manual(CN) Manual(CN) MSDS MSDS
Product Details Performance Procedures Citations
Product Details
Product Name in English:
Rat βTG/PBP/CXCL7/NAP2(Thromboglobulin, Beta) ELISA Kit
Species:
Rat
Alternative Name:
PPBP, B-TG1, Beta-TG, CTAP-III, CTAP3, CTAPIII, CXCL7, LA-PF4, LDGF, MDGF, NAP-2, PBP, SCYB7, TC1, TC2, TGB, TGB1, THBGB, THBGB1, pro-platelet basic protein
Assay Type:
Sandwich
Standard:
1000pg/mL
Sensitivity:
9.38 pg/mL
Detection Range:
15.63-1000pg/mL
Assay Time:
3.5H
Sample Type:
Serum, Plasma, Tissue homogenate and Other biological samples
Research:
Signal transduction;Infection immunity;Rheumatology;
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 βTG/PBP/CXCL7/NAP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to βTG/PBP/CXCL7/NAP2. 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 βTG/PBP/CXCL7/NAP2, 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 βTG/PBP/CXCL7/NAP2 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
1000 2.486 2.492 2.489 2.43
500 1.606 1.608 1.607 1.55
250 0.913 0.921 0.917 0.857
125 0.478 0.481 0.48 0.422
62.5 0.269 0.27 0.27 0.213
31.25 0.163 0.164 0.164 0.107
15.63 0.112 0.112 0.112 0.056
0 0.056 0.056 0.056 0
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 (%) 86-100 96-105 85-92
Average (%) 95 99 90
1:4 Range (%) 93-108 95-103 80-96
Average (%) 104 101 85
1:8 Range (%) 80-101 95-103 89-101
Average (%) 98 96 97
1:16 Range (%) 87-96 87-98 85-97
Average (%) 92 92 92
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) 80-97 88
EDTA plasma (n=8) 80-92 85
Cell culture media (n=8) 90-105 97
Assay Procedures
Related literature

Social Media