Alpha-Tubulin Housekeeping Cellular Kit
GAPDH Housekeeping Cellular Kit HTRF®
This assay enables measurement of the endogenous expression level of GAPDH in cells and tissues, to normalize data obtained on the protein(s) of interest.
- High sensitivity
This assay is designed to measure the endogenous expression level of GAPDH in cells and tissues, in order to normalize data obtained on the phospho- and/or total protein(s) of interest. Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH) is a key glycolytic enzyme which is constitutively and stably expressed in all cells and tissues. Its amino acid sequence exhibits a high degree of homology between mammalian species. These characteristics make it one of the most commonly used housekeeping proteins. Its concentration is proportional to cell numbers and total protein concentrations, and it is therefore used as an internal control for data normalization, to correct for signal changes caused by experimental variability (e.g. number of cells remaining in the culture plate after treatment, or lysis efficacy). The low sample volume of 4 µL and its compatibility with all HTRF phospho-total protein lysis buffers enable a multi-parametric analysis from the same lysate, with the detection of GAPDH in parallel with the phospho- and/or total protein(s) of interest.
- DATA NORMALIZATION
The GAPDH Housekeeping assay measures endogenous GAPDH in a cell or tissue lysate. Unlike Western Blot, the assay is entirely plate-based and does not require gels, electrophoresis, or transfer. The GAPDH Housekeeping assay uses two labeled antibodies: one coupled to a donor fluorophore, the other to an acceptor. Both antibodies are highly specific for a distinct epitope on the protein. In presence of GAPDH in a cell extract, the addition of these conjugates brings the donor fluorophore into close proximity with the acceptor and thereby generates a FRET signal. Its intensity is directly proportional to the concentration of the protein present in the sample, and provides a means of assessing any changes caused by experimental variability under a no-wash assay format.
The assay is run under a two-plate assay protocol, where cells are plated and treated in a culture plate. For the detection step, 4 µL of lysate are subsequently transferred into a low volume 96- or 384-well white plate, and 12 µL of kit diluent are added before the dispensing of 4 µL of HTRF® reagents. This protocol enables monitoring of the cells' viability and confluence in an appropriate cell culture plate.
The adherent cell lines HeLa (human), NIH-3T3 (mouse), GH1 (rat) and CHO-K1 (hamster) were plated in 96-well culture plates at different cell densities and incubated for 24 hours at 37°C-5% CO2. After culture medium removal, the cells were lysed with 50 µL of supplemented lysis buffer #1 (1X). The suspension human cell line Jurkat was dispensed under 30 µL in a 96-well half-area plate at different cell densities, incubated for 1h at 37°C-5% CO2, and directly lysed with 10 µL of supplemented lysis buffer #1 (4X). For HTRF detection of GAPDH levels, 4 µL of cell lysate (undiluted or prediluted in the supplemented lysis buffer) were transferred into a low volume white microplate and supplemented with 12 µL of diluent #11 before adding 4 µL of premixed detection antibodies. The HTRF signal was recorded after an overnight incubation at RT.
The HTRF GAPDH Housekeeping kit is adapted to adherent and suspension cells from different species. It has been validated on samples from human, mouse, rat and hamster origin, and is also compatible with monkey species. The assay range and sensitivity have been optimized on the most commonly used cell lines and cell densities. For some cell models that express high levels of GAPDH, the lysate must be prediluted in the supplemented lysis buffer 1X before transfer to the detection plate (e.g. 1/4 predilution for NIH-3T3 and CHO-K1 lysates; and 1/5 predilution for Jurkat cell lysates).
GH1 cells were plated at different cell densities in 96-well culture plates, grown for 24 hours at 37°C-5% CO2, and then lysed with HTRF Phospho-Total protein lysis buffer #1, #2, #3 or #4 (supplemented with the blocking reagent). For HTRF detection of GAPDH levels, 4 µL of cell lysate were transferred into a low volume white microplate and supplemented with 12 µL of diluent #11 before adding 4 µL of premixed detection antibodies. The HTRF signal was recorded after an overnight incubation at RT.
The assay is compatible with all Phospho-Total protein lysis buffers. The best performance is obtained with lysis buffer #1. However, the three other lysis buffers provide comfortable assay windows (S/N > 8), even on the lowest cell density. These results demonstrate that the GAPDH Housekeeping assay can be performed on the same lysate as the one used for Phospho- and Total protein assays. For more information, please refer to the lysis buffer compatibility table.
1. Study of ERK inhibition by the MEK inhibitor PD98059 in HeLa cells
HeLa cells were plated in a 96-well culture plate (100,000 cells/well) and incubated for 24 hours before treatment with increasing concentrations of the MEK inhibitor PD98059 for 30 minutes. After cell lysis with 50 µL of supplemented lysis buffer #1, the same lysate was sequentially dispensed into a low volume detection white plate: twice 16 µL for the combined analysis of phospho-ERK and total ERK levels using HTRF Advanced phospho-ERK and Total ERK kits (64AERPET/G/H and 64NRKPET/G/H), and an additional 4 µL (suplemented with 12 µL diluent #11) to control GAPDH levels using the HTRF GAPDH Housekeeping kit. The corresponding kit detection reagents were added under 4 µL and HTRF signals were recorded after an overnight incubation.
Increasing doses of PD98059 lead to increased inhibition of ERK phosphorylation. Since inhibition of ERK phosphorylation occurs without a decrease in total ERK or GAPDH levels, toxicity can be excluded from the list of possible mechanisms of action. Thus, it can be ascertained that PD98059 acts to decrease ERK phosphorylation primarily by targeting MEK, the kinase upstream of ERK.
2. Study of AKT activation by IGF-1 in HEK293 cells
HEK293 cells were plated in a 96-well culture plate (100,000 cells/well) and incubated for 24 hours before treatment with increasing concentrations of human IGF-1 for 10 minutes. After cell lysis with 50 µL of supplemented lysis buffer #1, the same lysate was sequentially dispensed into a low volume detection white plate: twice 16 µL for the combined analysis of phospho-AKT and total AKT levels using HTRF Phospho-AKT (Ser473) and Total AKT kits (64AKSPET/G/H and 64NKTPET/G/H), and an additional 4 µL (suplemented with 12 µL diluent #11) to control GAPDH levels using the HTRF GAPDH Housekeeping kit. The corresponding kit detection reagents were added under 4 µL and HTRF signals were recorded after an overnight incubation.
Cell stimulation with IGF-1 induces an increase in AKT phosphorylation on Ser473 and a down-regulation of AKT expression level, both in a dose-dependent manner with similar EC50 and IC50 values. On the other hand, the level of GAPDH remained unchanged, suggesting that the decrease in total AKT was not caused by an inhibition of global protein synthesis or by experimental issues. This example clearly illustrates the need to analyze the phospho- and total protein of interest, as well as GAPDH, in order to correctly understand the effect of compounds on the protein.
Lysates of Jurkat, CHO-K1, HeLa and NIH-3T3 cell lines plated at different cell densities in 96-well plates were prepared as described in the first section. The level of the housekeeping protein GAPDH was measured in these samples using the HTRF assay. In parallel, the concentration of proteins was determined from the same lysates using the BCA protein assay (QuantiPro™ BCA Assay Kit, Sigma-Aldrich) according to the manufacturer’s instructions. For both methods, lysates were analyzed either undiluted or prediluted in the appropriate buffer, thus ensuring all samples were tested within the respective assay linear ranges. Each graph represents the HTRF GAPDH Signal to Noise (S/N) versus the concentration of proteins determined by BCA. The cell densities used for the correlations are mentioned next to each point.
Using human, mouse or hamster cell lines, the level of GAPDH measured by HTRF is always properly correlated to the concentration of proteins determined by the BCA method (with correlation coefficients r > 0.97). These results demonstrate that GAPDH is an appropriate housekeeping protein suitable for checking the effect of compounds on protein(s) of interest.
Liver tissue samples from three different mice were homogenized with supplemented lysis buffer #3, and one rat liver tissue sample was lysed with supplemented lysis buffer #4. The samples were prepared and analyzed as described in the technical note. The level of the housekeeping protein GAPDH was measured in these samples using the HTRF assay. In parallel, the concentration of proteins was determined from the same lysates using the BCA protein assay (QuantiPro™ BCA Assay Kit, Sigma-Aldrich) according to the manufacturer’s instructions. For both methods, the lysates were analyzed after predilution in the appropriate buffer (dilution factor from 1/50 to 1/200), thus ensuring all samples were tested within the respective assay linear ranges.
The GAPDH Housekeeping assay is compatible with tissue lysates from different species. The assay sensitivity enables a comfortable detection of GAPDH in samples containing less than 0.1 mg/mL of proteins. The level of GAPDH measured by HTRF is always properly correlated to the concentration of proteins determined by the BCA method. These results demonstrate that GAPDH is an appropriate housekeeping protein that can be used to normalize tissue samples in order to study the effect of compounds on animal models.
Physiologically relevant results fo fast flowing research - Flyers
Insider Tips for successful sample treatment - Technical Notes
HTRF and WB compatible guidelines - Technical Notes
Protocol for tumor xenograft analysis with HTRF - Technical Notes
Mastering the art of cell signaling assays optimization - Guides
Multi-tissue cellular modeling and anlysis of insulin signaling - Posters
A solution for phospho-protein analysis in metabolic disorders - Posters
Detailed protocol and direct comparison with WB - Posters
A single technology for 2D cells, 3D cells, and xenograft models - Posters
PI3K/AKT/mTor translational control pathway - Posters
Analysis of a large panel of diverse biological samples and cellular models - Posters
One technology across all samples - Application Notes
Tumor xenograft analysis: HTRF versus Western blot - Application Notes
Valuable guidelines for efficiently analyzing and interpreting results - Application Notes
Increased flexibility of phospho-assays - Application Notes
Analyse of PI3K/AKT/mTor translational control pathway - Application Notes
In collaboration with Bayer - Scientific Presentations
A fun video introducing you to phosphorylation assays with HTRF - Videos
Seeding and lysing recommendations for a number of cell culture vessels. - Technical Notes
Combination of AlphaLISA®, HTRF®, or AlphaLISA® SureFire® Ultra™ immunoassays with the ATPlite™ 1step cell viability assay - Application Notes
Learn how to reduce time and sample consumption - Application Notes
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