Description
MAPKAPK5 (Phospho-Thr182)Colorimetric Cell-Based ELISA Kit
The MAPKAPK5 (Mitogen-Activated Protein Kinase-Activated Protein Kinase 5) Phospho-Thr182 Colorimetric Cell-Based ELISA Kit is a cutting-edge tool for the quantitative detection of phosphorylated MAPKAPK5 levels in cell lysates using a colorimetric method. This kit offers unparalleled sensitivity and specificity, allowing for accurate and reliable results in a variety of cell-based research applications.MAPKAPK5 is a key signaling protein that plays a crucial role in various cellular processes, including cell growth, proliferation, and stress response. Phosphorylation of MAPKAPK5 at threonine 182 is known to regulate its activity, making it an important marker for studying intracellular signaling pathways and potential therapeutic targets.
With its user-friendly protocol and robust performance, the MAPKAPK5 Phospho-Thr182 Colorimetric Cell-Based ELISA Kit is an indispensable tool for researchers looking to investigate the role of MAPKAPK5 in disease processes such as cancer, inflammation, and metabolic disorders. Unlock the mysteries of cellular signaling with this innovative ELISA kit from AssayGenie.
| Product Name: | MAPKAPK5 (Phospho-Thr182)Colorimetric Cell-Based ELISA Kit |
| Product Code: | CBCAB01681 |
| ELISA Type: | Cell-Based |
| Target: | MAPKAPK5 (Phospho-Thr182) |
| Reactivity: | Human, Mouse |
| Dynamic Range: | > 5000 Cells |
| Detection Method: | Colorimetric 450 nm |
| Format: | 2 x 96-Well Microplates |
The MAPKAPK5 (Phospho-Thr182) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect MAPKAPK5 protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated MAPKAPK5 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on MAPKAPK5 phosphorylation.
Qualitative determination of MAPKAPK5 (Phospho-Thr182) concentration is achieved by an indirect ELISA format. In essence, MAPKAPK5 (Phospho-Thr182) is captured by MAPKAPK5 (Phospho-Thr182)-specific primary (1ø) antibodies while the HRP-conjugated secondary (2ø) antibodies bind the Fc region of the 1ø antibody. Through this binding, the HRP enzyme conjugated to the 2ø antibody can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of the Cell-Based ELISA, multiple normalization methods are needed:
| 1. | A monoclonal antibody specific for human GAPDH is included to serve as an internal positive control in normalizing the target absorbance values. |
| 2. | Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method may be used to determine cell density. After staining, the results can be analysed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted. |
| Database Information: | Gene ID: 8550, UniProt ID: Q8IW41, OMIM: 606723, Unigene: Hs.413901 |
| Gene Symbol: | MAPKAPK5 |
| Sub Type: | Phospho |
| UniProt Protein Function: | MAPKAPK5: a member of the MAPKAPK family of protein kinases. Activated through phosphorylation by MAP kinases including ERK, p38-alpha, and MAPp38-beta In response to cellular stress and proinflammatory cytokines. Two alternately spliced transcript variants of this gene encoding distinct isoforms have been reported. |
| UniProt Protein Details: | Protein type:EC 2.7.11.1; Tumor suppressor; Kinase, protein; Protein kinase, Ser/Thr (non-receptor); Protein kinase, CAMK; CAMK group; MAPKAPK family; MAPKAPK subfamily Chromosomal Location of Human Ortholog: 12q24.13 Cellular Component: cytoplasm; cytosol; nucleoplasm; nucleus Molecular Function:calcium-dependent protein serine/threonine kinase activity; calmodulin binding; calmodulin-dependent protein kinase activity; MAP kinase kinase activity; p53 binding; protein binding; protein serine/threonine kinase activity Biological Process: negative regulation of TOR signaling pathway; peptidyl-serine phosphorylation; positive regulation of telomerase activity; positive regulation of telomere maintenance via telomerase; protein amino acid autophosphorylation; Ras protein signal transduction; regulation of translation; signal transduction |
| NCBI Summary: | The protein encoded by this gene is a tumor suppressor and member of the serine/threonine kinase family. In response to cellular stress and proinflammatory cytokines, this kinase is activated through its phosphorylation by MAP kinases including MAPK1/ERK, MAPK14/p38-alpha, and MAPK11/p38-beta. The encoded protein is found in the nucleus but translocates to the cytoplasm upon phosphorylation and activation. This kinase phosphorylates heat shock protein HSP27 at its physiologically relevant sites. Two alternately spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2012] |
| UniProt Code: | Q8IW41 |
| NCBI GenInfo Identifier: | 52000829 |
| NCBI Gene ID: | 8550 |
| NCBI Accession: | Q8IW41.2 |
| UniProt Secondary Accession: | Q8IW41,O60491, Q86X46, Q9BVX9, Q9UG86, B3KVA5, |
| UniProt Related Accession: | Q8IW41 |
| Molecular Weight: | 54,035 Da |
| NCBI Full Name: | MAP kinase-activated protein kinase 5 |
| NCBI Synonym Full Names: | mitogen-activated protein kinase-activated protein kinase 5 |
| NCBI Official Symbol: | MAPKAPK5 |
| NCBI Official Synonym Symbols: | MK5; MK-5; PRAK; MAPKAP-K5 |
| NCBI Protein Information: | MAP kinase-activated protein kinase 5 |
| UniProt Protein Name: | MAP kinase-activated protein kinase 5 |
| UniProt Synonym Protein Names: | p38-regulated/activated protein kinase; PRAK |
| Protein Family: | MAP kinase-activated protein kinase |
| UniProt Gene Name: | MAPKAPK5 |
| UniProt Entry Name: | MAPK5_HUMAN |
| Component | Quantity |
| 96-Well Cell Culture Clear-Bottom Microplate | 2 plates |
| 10X TBS | 24 mL |
| Quenching Buffer | 24 mL |
| Blocking Buffer | 50 mL |
| 15X Wash Buffer | 50 mL |
| Primary Antibody Diluent | 12 mL |
| 100x Anti-Phospho Target Antibody | 60 µL |
| 100x Anti-Target Antibody | 60 µL |
| Anti-GAPDH Antibody | 60 µL |
| HRP-Conjugated Anti-Rabbit IgG Antibody | 12 mL |
| HRP-Conjugated Anti-Mouse IgG Antibody | 12 mL |
| SDS Solution | 12 mL |
| Stop Solution | 24 mL |
| Ready-to-Use Substrate | 12 mL |
| Crystal Violet Solution | 12 mL |
| Adhesive Plate Seals | 2 seals |
The following materials and/or equipment are NOT provided in this kit but are necessary to successfully conduct the experiment:
- Microplate reader able to measure absorbance at 450 nm and/or 595 nm for Crystal Violet Cell Staining (Optional)
- Micropipettes with capability of measuring volumes ranging from 1 µL to 1 ml
- 37% formaldehyde (Sigma Cat# F-8775) or formaldehyde from other sources
- Squirt bottle, manifold dispenser, multichannel pipette reservoir or automated microplate washer
- Graph paper or computer software capable of generating or displaying logarithmic functions
- Absorbent papers or vacuum aspirator
- Test tubes or microfuge tubes capable of storing ≥1 ml
- Poly-L-Lysine (Sigma Cat# P4832 for suspension cells)
- Orbital shaker (optional)
- Deionized or sterile water
*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
| Step | Procedure |
| 1. | Seed 200 µL of 20,000 adherent cells in culture medium in each well of a 96-well plate. The plates included in the kit are sterile and treated for cell culture. For suspension cells and loosely attached cells, coat the plates with 100 µL of 10 µg/ml Poly-L-Lysine (not included) to each well of a 96-well plate for 30 minutes at 37 °C prior to adding cells. |
| 2. | Incubate the cells for overnight at 37 °C, 5% CO2. |
| 3. | Treat the cells as desired. |
| 4. | Remove the cell culture medium and rinse with 200 µL of 1x TBS, twice. |
| 5. | Fix the cells by incubating with 100 µL of Fixing Solution for 20 minutes at room temperature. The 4% formaldehyde is used for adherent cells and 8% formaldehyde is used for suspension cells and loosely attached cells. |
| 6. | Remove the Fixing Solution and wash the plate 3 times with 200 µL 1x Wash Buffer for five minutes each time with gentle shaking on the orbital shaker. The plate can be stored at 4 °C for a week. |
| 7. | Add 100 µL of Quenching Buffer and incubate for 20 minutes at room temperature. |
| 8. | Wash the plate 3 times with 1x Wash Buffer for 5 minutes each time. |
| 9. | Add 200 µL of Blocking Buffer and incubate for 1 hour at room temperature. |
| 10. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 11. | Add 50 µL of 1x primary antibodies Anti-MAPKAPK5 (Phospho-Thr182) Antibody, Anti-MAPKAPK5 Antibody and/or Anti-GAPDH Antibody) to the corresponding wells, cover with Parafilm and incubate for 16 hours (overnight) at 4 °C. If the target expression is known to be high, incubate for 2 hours at room temperature. |
| 12. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 13. | Add 50 µL of 1x secondary antibodies (HRP-Conjugated AntiRabbit IgG Antibody or HRP-Conjugated Anti-Mouse IgG Antibody) to corresponding wells and incubate for 1.5 hours at room temperature. |
| 14. | Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time. |
| 15. | Add 50 µL of Ready-to-Use Substrate to each well and incubate for 30 minutes at room temperature in the dark. |
| 16. | Add 50 µL of Stop Solution to each well and read OD at 450 nm immediately using the microplate reader. |
(Additional Crystal Violet staining may be performed if desired – details of this may be found in the kit technical manual.)
