NF-kB Leeporter™ Luciferase Reporter-HEK293 Cell Line

Fig-1: Dose response EC50 evaluation of NF-kB reporter HEK293 cells against phorbol 12-myristate 13-acetate (PMA).

NF-kB Leeporter™ Luciferase Reporter-HEK293 Cell Line

Roll over image to zoom in

Fig-1: Dose response EC50 evaluation of NF-kB reporter HEK293 cells against phorbol 12-myristate 13-acetate (PMA).

Fig-2: Normalized fold induction of NF-kB activity against PMA in NF-kB reporter HEK293 cells.

Fig-3: Dose response EC50 evaluation of NF-kB reporter HEK293 cells against TNF-alpha.

Fig-4: Normalized fold induction of NF-kB activity against TNF-alpha in NF-kB reporter HEK293 cells.

Product code: 14-125ACL

Application :	Functional Assay

Shipping Info:

Order now and get it on Tuesday November 26, 2024

Download TDS / Manual MSDS

Write a review for this product on BioCompare

Get $20 gift card from Amazon

Shipping Info:

Order now and get it on Tuesday November 26, 2024

Same day delivery FREE on San Diego area orders placed by 1.00 PM

Download TDS / Manual MSDS

Amount :	1 Vial
Content :	Each vial contains 2 ~ 3 x 10^6 cells in 1 ml of 90% FBS + 10% DMSO.
Storage condition :	Immediately upon receipt, store in liquid nitrogen.

The NF-kB Leeporter™ Luciferase Reporter cell line is a stably transfected HEK293 cell line which expresses Renilla luciferase reporter gene under the transcriptional control of the NF-kB response element. NF-kB is a key transcription factor that is involved in immune and inflammatory responses, developmental processes, cellular growth and apoptosis. The NF-kB induction assays were performed with phorbol 12-myristate 13-acetate (PMA) (Figures 1 and 2) and with TNF-alpha (Figures 3 and 4).

Application:

Monitor the NF-kB signaling pathway.
Screen for activators or inhibitors of the NF-kB signaling pathway.

Culture conditions:

Cells should be grown at 37^oC with 5% CO₂ using DMEM medium (w/ L-Glutamine, 4.5g/L Glucose and Sodium Pyruvate) supplemented with 10% heat-inactivated FBS and 1% Pen/Strep, plus 3 µg/ml of Puromycin (Note: Puromycin can be omitted during the reporter cell assays).

It is recommended to quickly thaw the frozen cells upon receipt or from liquid nitrogen in a 37^oC water-bath, transfer to a tube containing 10 ml of growth medium without Puromycin, spin down cells, resuspend cells in pre-warmed growth medium without Puromycin, transfer resuspended cells to T25 flask and culture in 37^oC-CO₂ incubator.

Leave the T25 flask in the incubator for 1~3 days without disturbing or changing the medium until cells completely recover viability and become adherent. Once cells are over 90% adherent, remove growth medium and passage the cells through trypsinization and centrifugation. At first passage, switch to growth medium containing Puromycin. Cells should be split before they reach complete confluence.

To passage the cells, detach cells from culture vessel with Trypsin/EDTA, add complete growth medium and transfer to a tube, spin down cells, resuspend cells and seed appropriate aliquots of cells suspension into new culture vessels. Subcultivation ration = 1:10 to 1:20 weekly. To achieve satisfactory results, cells should not be passaged over 16 times.

Functional validation:

A. Response of NF-kB Leeporter™ – HEK293 cells to phorbol 12-myristate 13-acetate (PMA).

1. Harvest NF-kB Leeporter™ – HEK293 cells and seed cells into a white solid-bottom 96-well microplate in 100 µl of growth medium at 5 x 10^4 cells/well.

2. Incubate cells at 37^oC in a CO₂ incubator for overnight.

3. The next day, stimulate cells with different concentrations of PMA.

4. Incubate at 37^oC in a CO₂ incubator for 16 hours.

5. Equilibrate the plate to room temperature for 10 minutes.

6. Add 50 µl of luciferase assay reagent (Abeomics, Cat #17-1101; Refer to the reagent datasheet for the detailed luciferase assay protocol) per well.

7. Read the plate in 1-5 minutes to measure luminescence using a microplate luminometer.

LIMITED USE RESTRICTIONS:

THIS PRODUCT IS SOLELY FOR IN VITRO RESEARCH USE ONLY. NOT FOR DIAGNOSTIC OR THERAPEUTIC USE.

By use of this product, user agrees to be bound by the terms of this limited use statement.

This product is solely for Internal Research Purposes and not for Commercial Purposes. Commercial Purposes include, but are not limited to (1) use of the cell line in manufacturing; (2) use of the cell line to provide a service, information or data; (3) use of the cell line for therapeutic, diagnostic or prophylactic purposes; or (4) resale of the cell line whether or not such cell lines are resold for use in research. The buyer cannot sell, give or otherwise transfer this product to a third party.

Commercial License Agreement is available for non-research use if applicable. Please contact Abeomics ([email protected]).

For Research Use Only. Not for use in diagnostic/therapeutics procedures.

1. Piri-Gharaghie T, Doosti A, Mirzaei SA.
Novel adjuvant nano-vaccine induced immune response against Acinetobacter baumannii.
AMB Express. 2023 Mar 11;13(1):31. doi: 10.1186/s13568-023-01531-0.
PMID: 36905472; PMCID: PMC10008545.

2. Wang F, Stappenbeck F, Tang LY, Zhang YE, Hui ST, Lusis AJ, Parhami F.
Oxy210, a Semi-Synthetic Oxysterol, Exerts Anti-Inflammatory Effects in Macrophages via Inhibition of Toll-like Receptor (TLR) 4 and TLR2 Signaling and Modulation of Macrophage Polarization.
Int J Mol Sci. 2022 May 13;23(10):5478. doi: 10.3390/ijms23105478.
PMID: 35628290; PMCID: PMC9141227.

There are currently no product reviews

Write a review on this product!