Description
Key facts
Detection method:Colorimetric,
Sample types:Nuclear Extracts,
Reacts with:Mouse, Rat, Human,
Assay type:Semi-quantitative,
Sensitivity:= 600 ng/well,
Assay time:3h 30m,
Assay Platform:Microplate reader
Product details:
NFATc1 Transcription Factor Assay Kit (Colorimetric) (ab207215) is a high throughput assay to quantify NFATc1 activation in nuclear extracts. This assay combines a quick ELISA format with a sensitive and specific non-radioactive assay for transcription factor activation.
A specific double stranded DNA sequence containing the NFATc1 consensus binding site (5' –AGGAAA– 3') has been immobilized onto a 96-well plate. Active NFATc1 present in the nuclear extract specifically binds to the oligonucleotide. NFATc1 is detected by a primary antibody that recognizes an epitope of NFATc1 accessible only when the protein is activated and bound to its target DNA. An HRP-conjugated secondary antibody provides sensitive colorimetric readout at OD 450 nm. This product detects human and mouse NFATc1.
Key performance and benefits:
Assay time: 3.5 hours (cell extracts preparation not included).
Detection limit: < 0.6 μg nuclear extract/well.
Detection range: 0.6 – 10 μg nuclear extract/well.
NFAT proteins are transcription factors that were first identified as inducers of the immune response. As demonstrated later, these proteins also play varied roles in cell differentiation and adaptation for vascular endothelial cells or skeletal muscle cells. There are four NFAT family members (NFAT1-4, NFAT2 is also called NFATc or NFATc1) from which numerous isoforms are generated by alternative splicing1. NFAT mRNAs are found in peripheral blood lymphocytes, spleen (NFAT1 and 2) and thymus (NFAT4). NFATs modulate the expression of numerous cytokines such as IL-2, IL-3, IL-4, IL-5, IL-8, IL-13, GM-CSF, IFNa, IFNg and CD40L. In resting cells, NFATc1 is confined to the cytoplasm, where it is maintained in a phosphorylated state by the action of constitutive kinases. Upon stimulation, NFATc1 is dephosphorylated by calcineurin, a Ca2+-dependent phosphatase, and migrates to the nucleus. NFATc1 dephosphorylation is stimulated by Ca2+-coupled membrane receptors, such as T cell and B cell receptors, and the CD40, FceRI, CD16 and G protein-associated receptors (thrombin or H1 histamine receptors). NFATc1 can also be activated by calcium ionophores. Cyclosporin A and FK506 immunosuppressor drugs inhibit calcineurin activity on NFAT. Receptors not associated with calcium movement are not expected to stimulate NFAT. When calcium levels drop, calcineurin becomes inactive, and NFATc1 is rephosphorylated by kinases and exported back into the cytoplasm.
NFAT phosphoproteins share two conserved domains: a DNA-binding domain (DBD) displaying limited similarity to the Rel protein family DBD, and modulating interactions with AP-1 dimers; and a NFAT homology region (NHR), upstream of the DBD that regulates translocation and DNA-binding activity. The regulatory domain is dephosphorylated by the calcium- and calmodulin-dependent phosphatase calcineurin, which controls NFAT nuclear translocation. Transactivation domains can be found at the N- and C-terminal ends of the NFAT proteins. NFATs bind to the DNA consensus motif 5´-T/AGGAAA-3´ as monomers. NFATs can cooperatively interact with AP-1 and GATA proteins for DNA binding. NFAT can also bind to certain kB-like sites. Vitamin D3 receptor heterodimers (RXR:VDR) can abrogate NFAT modulation of IL-2 by binding to a site which overlaps the NFAT distal site. Sites in IL-2 and GM-CSF promoters can accommodate both NFAT and the Ets-family member, Elf-1.
Properties and Storage Information:
Shipped at conditions-Dry Ice, Appropriate short-term storage conditions-Multi, Appropriate long-term storage conditions-Multi, Storage information-Please refer to protocols
