Antigen Information
- P23771
- 2625
- GATA3
- Human
Assay Format
- Human
- Cell Lysates
- Nuclear Extracts
- Sandwich-based
- Semi-Quantitative
Product Specifications
Introduction
Product Features
- Specific transcription factor-DNA binding assay
- Perfect alternative to EMSA
- Easy to perform in an ELISA format
- Non-radioactive assay
- High throughput (96-well plate format)
- Assay can be completed within 5 hours
Application Notes
- 96-well Strip Microplate pre-coated with DNA probes
- DNA Binding Buffer
- Positive Control Sample
- Specific Competitor DNA probe
- Non-specific Competitor DNA probe
- Assay Reagent
- DTT
- Wash Buffer
- Primary Antibody
- HRP-conjugated Secondary Antibody
- Antibody Diluent Buffer
- TMB One-Step Substrate Reagent
- Stop Solution
- Distilled or deionized water
- 100 ml and 1 liter graduated cylinders
- Tubes to prepare sample dilutions
- Absorbent paper
- Precision pipettes to deliver 2 µl to 1 ml volumes
- Adjustable 1-25 ml pipettes for reagent preparation < li="">
- Microplate reader capable of measuring absorbance at 450 nm
- Prepare all reagents and samples as instructed in the manual.
- Add 100 µl of sample or positive control to each well.
- Incubate 2 h at RT or O/N at 4 °C.
- Add 100 µl of prepared primary antibody to each well.
- Incubate 1 h at RT.
- Add 100 µl of prepared HRP-secondary antibody to each well.
- Incubate 1 h at RT.
- Add 100 µl of TMB One-Step Substrate Reagent to each well.
- Incubate 30 min at RT.
- Add 50 µl of Stop Solution to each well.
- Read at 450 nm immediately.
Typical Data
Figure 1Transcription factor activity assay of GATA-3 from nuclear extracts of Jurkat cells or HeLa cells. In Jurkat cells, activated GATA-3 is translocated into the nucleus where it binds with its corresponding DNA. A. Western-blot result of GATA-3 from cytoplasmic and nuclear fractions. B. Transcription factor activity assay of GATA-3 from nuclear fractions with the RayBio® GATA-3 Transcription Factor-Activity Assay Kit.
Figure 2Transcription factor activity assay of GATA-3 from nuclear extracts of Jurkat cells or HeLa cells with the specific competitor or non-specific competitor. The result shows specific binding of GATA-3 to the GATA conserved binding site detected by using the RayBio® GATA-3 Transcription Factor-Activity Assay Kit.
Storage/Stability
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