This kit was based on sandwich ELISA method. The experiment lasted 120 minutes. Capture antibody was conjugated to an affinity tag that was recognized by a specific antibody coated on the QuickTest plate. Add the Cap/Det Ab working solution into each well, then add the standards and pilot samples into individual wells. If the sample contains EGR1, a capture antibody-EGR1-biotin-detection antibody complex was formed. After incubation, unbound conjugates were removed by wash buffer. HRP-Streptavidin was added. After washing, TMB substrates were added to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that turned yellow after adding a stop solution. Read the O.D. absorbance at 450nm in a microplate reader. The concentration of EGR1 in the sample was calculated by drawing a standard curve. The concentration of the target substance is proportional to the OD450 value.
Alternative Names
Early growth response protein 1 ELISA Kit, EGR-1 ELISA Kit, AT225 ELISA Kit, Nerve growth factor-induced protein A ELISA Kit, NGFI-A ELISA Kit, Transcription factor ETR103 ELISA Kit, Transcription factor Zif268 ELISA Kit, Zinc finger protein 225 ELISA Kit, Zinc finger protein Krox-24 ELISA Kit, EGR1 ELISA Kit, KROX24 ELISA Kit, ZNF225 ELISA Kit
Reactivity
Rat
Detection Method
Double Antibody
Detection Range
6.25-400pg/ml
Assay Type
Sandwich
Assay Duration
120 minutes
Kit Components
Kit Components
Item
Size(48T)
Size(96T)
Storage Condition for Opened Kit
E001
ELISA Microplate(Dismountable)
8x6
8x12
Put the rest strips into a sealed foil bag with the desiccant. Stored for 1 month at 2-8°C; Stored for 6 month at -20°C
E002
Lyophilized Standard
1vial
2vial
Put the rest standards into a desiccant bag. Stored for 1 month at 2-8°C; Stored for 6 month at -20°C
E054
Cap/Det Ab (Ready to use, blue)
3ml
6ml
2-8°C (Avoid Direct Light)
E053
HRP-Streptavidin (Ready to use, orange)
5ml
10ml
E024
TMB Substrate
5ml
10ml
E039
Sample Dilution Buffer
20ml
20ml
2-8°C
E026
Stop Solution
5ml
5ml
E038
Wash Buffer(25X)
15ml
30ml
E006
Plate Sealer
3 pieces
5 pieces
E007
Product Description
1 copy
1 copy
Recovery
Add a certain amount of EGR1 into the sample. Calculate the recovery by comparing the measured value with the expected amount of EGR1 in the sample.
Sample Type
Recovery Range(%)
Average(%)
serum(n=10)
85-98
91
EDTA plasma(n=10)
86-105
98
Heparin plasma(n=10)
86-97
93
Linearity
Dilute the sample with a certain amount of EGR1 at 1:2, 1:4 and 1:8 to get the recovery range.
Sample Type
1:2
1:4
1:8
serum(n=10)
85-105%
94-105%
90-100%
EDTA plasma(n=10)
83-101%
83-97%
84-95%
Heparin plasma(n=10)
81-99%
82-94%
82-93%
Sensitivity
3.75pg/ml
Specificity
Specifically binds with EGR1 , no obvious cross reaction with other analogues.
Standard Curve
This product is detected by QC department and meets performance required in the manual. (Laboratory Humidity: 20%-60%; Temperature: 18°C -25°C; Equilibrate TMB substrate to 37°C before staining. After adding into the ELISA wells, incubate for 15min at 37°C in dark.) Due to different assay environments and operations, assay data below and standard curve are provided for reference. Experimenters should establish standard curve according to their own assay.
STD.(pg/ml)
OD-1
OD-2
Average
0
0.067
0.069
0.068
6.25
0.176
0.175
0.176
12.5
0.273
0.268
0.271
25
0.512
0.508
0.49
50
0.886
0.879
0.84
100
1.262
1.272
1.298
200
2.117
2.136
2.081
400
2.686
2.621
2.64
Assay Procedure Summary
Step 1: Take out the required plate wells, add 50ul Cap/Det Ab into each well, then add 50ul Standard or Sample into individual well. (When adding standard or sample, the disposable tip lightly touches the liquid level. Change the disposable tips for different samples and standards.) Gently tap the plate for 10s to ensure thorough mixing then static incubate for 60 minutes at 37°C.
Washing: Wash the plate twice without immersion.
Step 2: Add 100ul HRP-Streptavidin (orange) into each well, seal the plate and static incubate for 30 minutes at 37°C.
Washing: Wash the plate five times without immersion.
Step 3: Add 90ul TMB substrate solution, seal the plate and static incubate for 10-20 minutes at 37°C. (Accurate TMB visualization control is required.)
Step 4: Add 50ul stop solution. Read at 450nm immediately and calculate.
Stability
Perform the stability test for the sealed kit at 37°C and 2-8°C and get relevant data.
ELISA kit(n=5)
37°C for 1 month
2-8°C for 6 months
Average(%)
80
95-100
UniProt ID
P08154
Antigen
EGR1
Usage Notes
Microplate reader (wavelength: 450nm) 37°C incubator (CO2 incubator for cell culture is not recommenced.) Automated plate washer or multi-channel pipette/5ml pipettor (for manual washing purpose) Precision single (0.5-10uL, 5-50uL, 20-200uL, 200-1000uL) and multi-channel pipette with disposable tips(Calibration is required before use.) Sterile tubes and Eppendorf tubes with disposable tips Absorbent paper and loading slot Deionized or distilled water
Intra-assay Precision: samples with low, medium and high concentration are tested 20 times on the same plate. Inter-assay Precision: samples with low, medium and high concentration are tested 20 times on three different plates.
Item
Intra-assay Precision
Inter-assay Precision
Sample
1
2
3
1
2
3
n
20
20
20
20
20
20
Mean (pg/ml)
13.05
48.73
207.37
11.59
51.79
193.26
Standard deviation
0.52
1.78
7.47
0.47
1.89
7.9
CV(%)
3.99
3.66
3.6
4.02
3.65
4.09
Storage
2-8°C(Sealed), Don't cryopreserve.
Reviews of Rat EGR1 (Early Growth Response Protein 1) QuickTest ELISA Kit