Leeporter™ Renilla Luciferase Assay Reagent- 1000 Test
Leeporter™ Luciferase Assay Reagent- 1000 Test
Referência 17-1101
Tamanho : 1kit
Marca : Abeomics
Contactar o distribuidor local :
Telefone : +1 850 650 7790
| Amount : | 1 kit |
| Content : | 1000 test (96-well plate format). Assay buffer contains 0.01% Sodium Azide. |
| Storage condition : | Store at -20°C |
The Leeporter™ Renilla Luciferase Assay Reagent was specifically formulated to use with our Leeporter™ (Luciferase Reporter) Cell Lines expressing an optimized intracellular Renilla luciferase, which was designed to produce highly sensitive signal and prolonged signal intensity. As a one-step glow assay reagent, the Leeporter™ Luciferase Assay Reagent can be directly added to cell culture plates compatible with the luminometer being used without diluting or transferring culture supernatants or cell lysates to other plates.
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Protocol:
1) Substrate (100X) Reconstitution:
Add 0.5 ml Substrate Reconstitution Solution to lyophilized Substrate vial and dissolve thoroughly by gently pipetting up and down, and/or inverting tubes. The reconstituted 100X substrate may be stored in a dark environment at -20oC for up to one month.
2) Assay Buffer:
Thaw Assay Buffer of 50 ml in room temperature water bath and dissolve thoroughly any precipitates by swirling and/or gentle vortexing until solution becomes clear. Assay Buffer can be aliquoted (e.g. 5-10 ml each) and stored at -20oC for several months.
3) Preparation of complete Assay Solution (for 96-well plate format):
Prepare complete Assay Solution fresh for each use, which should be used within 2 hours. Thaw Assay Buffer and equilibrate to room temperature with swirling and/or gentle vortexing. Calculate how much complete assay solution is needed (Note: 50 ul of complete assay solution is required for each well of 96-well plate). Aliquot proper amount of Assay Buffer in a 15 ml tube and add corresponding amount of reconstituted 100X substrate to make a final 1X substrate assay solution.
4) Luciferase Assay (96-well plate format):
1. Plate you target Leeporter™ Luciferase reporter cells in a white solid-bottom 96-well microplate (Note: The 96-well plate used should be compatible with the luminometer being used.) at 100 ul cells/well, based on the corresponding protocol to your target Leeporter™ cell line (Note: Each target Leeporter™ cell line protocol can be found in its corresponding Data Sheets.). [Total volume per well is 100 uL]
2. Stimulate or treat your target cells based on the corresponding protocol to your target Leeporter™ cell line. [Total volume per well becomes 105~110 uL = 100 ul cells + 5~10 ul treatment]
3. After completion of stimulation/treament of your target cells, equilibrate the 96-well plate containing your target cells being assayed to room temperature for 10 minutes (Note: Do NOT remove or disturb cell culture medium.).
4. Using a multi-channel pipettor, add 50 ul complete Assay Solution directly to each plate well (Note: Do NOT remove cell culture medium when adding the Assay Reagent. So the Assay Reagent of 50 ul should be directly added on top of the cell culture of each well.). [Total volume per well becomes 155~160 uL = 100 ul cells + 5~10 ul treatment + 50 ul complete assay solution]
5. Use automix for 2-3 seconds, and then read the plate in a luminometer within 1-5 minutes. (An example of a luminometer set up: SpectraMaxL (Molecular Devices): target wavelength of 470nm, integration time at 0.5 sec and automix for 2 sec).
For Research Use Only. Not for use in diagnostic/therapeutics procedures.
1. Suzuki R, Mishima M, Nagane M, Mizugaki H, Suzuki T, Komuro M, Shimizu T, Fukuyama T, Takeda S, Ogata M, Miyamoto T, Aihara N, Kamiie J, Kamisuki S, Yokaryo H, Yamashita T, Satoh T.
The novel sustained 3-hydroxybutyrate donor poly-D-3-hydroxybutyric acid prevents inflammatory bowel disease through upregulation of regulatory T-cells.
FASEB J. 2023 Jan;37(1):e22708. doi: 10.1096/fj.202200919R.
PMID: 36562544.
2. Hratch Matthew Baghdassarian
Understanding How Context Influences Function Across Biological Scales in Multicellular Mammalian Systems
A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Bioinformatics and Systems Biology UNIVERSITY OF CALIFORNIA SAN DIEGO
https://escholarship.org/content/qt91m6s7f8/qt91m6s7f8_noSplash_4ebef6c201c519213351d0b4ac89e7ba.pdf?t=s29esl
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