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Catalog Number:RE2999H
Human TAF2(Transcription initiation factor TFIID subunit 2) ELISA Kit

Size:

48 T

96 T

Price:

$279.00

$399.00

Delivery: Order now, ship in 3 days

Product Details
Product Name Human TAF2(Transcription initiation factor TFIID subunit 2) ELISA Kit Species Human
Uniprot ID N/A Alternative Names Transcription initiation factor TFIID subunit 2,CIF15, MRT4, TAF2B, TAFII15,15 kDa cofactor of initiator function,RNA polymerase II TBP-associated factor subunit B,TBP-associated factor 15 kDa,Transcription initiation factor TFIID 15 kDa subunit,TAF(II)15,TAFII-15,TAFII15
Detection method Sandwich Sensitivity 9.38 pg/mL
Standard 1000pg/mL Detection Range 15.63-1000pg/mL
Sample type Serum, Plasma, Tissue homogenate and Other biological samples;Sample Volume=100μL
Reaction time 3.5H Research Area Neuro science;
Test principle This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human TAF2. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human TAF2 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human TAF2, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human TAF2. You can calculate the concentration of Human TAF2 in the samples 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.

(pg/mL) OD Corrected
1000.00 2.499 2.430
500.00 1.619 1.550
250.00 0.926 0.857
125.00 0.491 0.422
62.50 0.282 0.213
31.25 0.176 0.107
15.63 0.125 0.056
0.00 0.069 0.000
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.

Intra-assay Precision Inter-assay Precision
Sample 1 2 3 1 2 3
n 20 20 20 20 20 20
Mean(pg/mL) 31.12 198.21 378.57 21.02 186.65 460.59
Standard deviation 1.13 12.00 23.95 1.59 12.02 20.95
C V (%) 3.87 6.19 6.83 4.07 5.25 4.81
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) 83-98 90
EDTA plasma (n=8) 81-95 88
Cell culture media (n=8) 88-102 95
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 (%) 90-98 80-95 85-97
Average (%) 93 84 88
1:4 Range (%) 85-92 96-105 93-101
Average (%) 92 101 100
1:8 Range (%) 83-96 85-96 97-103
Average (%) 87 88 102
1:16 Range (%) 93-102 90-99 91-99
Average (%) 101 98 95
Assay Procedures