Mouse Cell Biology ELISA Kits 1
Mouse Estrogen ELISA Kit (MOFI01442)
- SKU:
- MOFI01442
- Product Type:
- ELISA Kit
- Size:
- 96 Assays
- Sensitivity:
- 9.375pg/ml
- Range:
- 15.625-1000pg/ml
- ELISA Type:
- Competitive
- Synonyms:
- Estrogen
- Reactivity:
- Mouse
Description
Mouse Estrogen ELISA Kit
Estrogen is a hormone that plays a crucial role in the development and functioning of the female reproductive system. Estrogen is responsible for regulating the menstrual cycle, promoting the development of secondary sexual characteristics in females, and supporting pregnancy. The Assay Genie Mouse Estrogen ELISA Kit is specifically designed for the quantitative measurement of estrogen levels in mouse biological samples, such as serum, plasma, and tissue homogenates and serves as a valuable tool for studying the role of estrogen in various research areas, including reproductive biology, endocrinology, cancer research, and hormonal regulation.
Key Features
Save Time | Pre-coated 96 well plate | |
Quick Start | Kit includes all necessary reagents | |
Publication Ready | Reproducible and reliable results |
Overview
Product Name: | Mouse Estrogen ELISA Kit (MOFI01442) |
Product Code: | MOFI01442 |
Size: | 96 Assays |
Alias: | Estrogen ELISA Kit |
Detection Method: | Competitive ELISA |
Application: | This immunoassay kit allows for the in vitro quantitative determination of Mouse Estrogen concentrations in serum plasma and other biological fluids. |
Sensitivity: | < 9.375pg/ml |
Range: | 15.625-1000pg/ml |
Storage: | 4°C for 6 months |
Note: | For Research Use Only |
Additional Information
Recovery | Matrices listed below were spiked with certain level of Mouse Estrogen and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse Estrogen in samples. (Not Available.) |
Linearity: | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse Estrogen and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected. (Not Available) |
Intra Assay | CV < 8% |
Inter Assay | CV < 10% |
Kit Components
Component | Quantity | Storage |
ELISA Microplate (Dismountable) | 8x12 strips | 4°C for 6 months |
Lyophilized Standard | 2 | 4°C/ -20°C |
Sample/Standard Dlution Buffer | 20ml | 4°C |
Biotin-labeled Antibody (Concentrated) | 120ul | 4°C (Protection from light) |
Antibody Dilution Buffer | 10ml | 4°C |
HRP-Streptavidin Conjugate (SABC) | 120ul | 4°C (Protect from light) |
SABC Dilution Buffer | 10ml | 4°C |
TMB Substrate | 10ml | 4°C (Protection from light) |
Stop Solution | 10ml | 4°C |
Wash Buffer (25X) | 30ml | 4°C |
Plate Sealer | 5 | - |
Other materials required:
- Microplate reader with 450 nm wavelength filter
- Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
- Incubator
- Deionized or distilled water
- Absorbent paper
- Buffer resevoir
Protocol
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
Equilibrate the TMB substrate for at least 30 min at 37°C beforeuse. When diluting samples and reagents, they must be mixed completely andevenly. It is recommended to plot a standard curve for each test.
Step | Procedure |
1. | Set standard, test sample and control (zero) wells on the pre-coatedplate respectively, and then, record their positions. It isrecommended to measure each standard and sample in duplicate. Washplate 2 times before adding standard, sample and control (zero) wells! |
2. | Add Sample and Biotin-detection antibody: Add 50µL of Standard, Blank or Sample per well. The blankwell is added with Sample Dilution Buffer. Immediately add 50 µL of biotin-labelled antibody workingsolution to each well. Cover with the plate sealer provided. Gently tap the plate to ensure thoroughmixing. Incubate for 45 minutes at 37°C. (Solutions are added to the bottom of micro-ELISA platewell, avoid touching plate walls and foaming). |
3. | Wash: Aspirate each well and wash, repeating the process three timesWash by filling each well with Wash Buffer (approximately 350µL)using a squirt bottle, multi-channel pipette, manifold dispenser orautomated washer. Complete removal of liquid at each step is essentialto good performance. After the last wash, remove any remaining WashBuffer by aspirating or decanting. Invert the plate and pat it againstthick clean absorbent paper. |
4. | HRP-Streptavidin Conjugate(SABC): Add 100µL of SABC workingsolution to each well. Cover with a new Plate sealer. Incubate for30minutes at 37°C. |
5. | Wash: Repeat the aspiration/wash process for five times. |
6. | TMB Substra |