Description
MARCKS (Phospho-Ser158)Colorimetric Cell-Based ELISA Kit
The MARCKS Phospho-Ser158 Colorimetric Cell-Based ELISA Kit is a powerful tool for researchers looking to accurately measure levels of MARCKS (Myristoylated Alanine-Rich C-Kinase Substrate) phosphorylated at serine 158 in cell lysates. With its high sensitivity and specificity, this kit provides reliable and reproducible results for a variety of research applications.MARCKS is a key protein involved in cellular signaling pathways and plays a crucial role in processes such as cell motility, adhesion, and membrane trafficking.
Phosphorylation of MARCKS at serine 158 is known to regulate its function and influence cell behavior, making it an important target for study in the fields of cancer, neurobiology, and cell biology.By using the MARCKS Phospho-Ser158 Colorimetric Cell-Based ELISA Kit, researchers can gain valuable insights into the role of MARCKS phosphorylation in cellular processes and disease states, ultimately leading to a better understanding of potential therapeutic interventions.
| Product Name: | MARCKS (Phospho-Ser158)Colorimetric Cell-Based ELISA Kit |
| Product Code: | CBCAB01562 |
| ELISA Type: | Cell-Based |
| Target: | MARCKS (Phospho-Ser158) |
| Reactivity: | Human, Mouse, Rat |
| Dynamic Range: | > 5000 Cells |
| Detection Method: | Colorimetric 450 nm |
| Format: | 2 x 96-Well Microplates |
The MARCKS (Phospho-Ser158) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect MARCKS protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated MARCKS in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on MARCKS phosphorylation.
Qualitative determination of MARCKS (Phospho-Ser158) concentration is achieved by an indirect ELISA format. In essence, MARCKS (Phospho-Ser158) is captured by MARCKS (Phospho-Ser158)-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: 4082, UniProt ID: P29966, OMIM: 177061, Unigene: Hs.519909/Hs.712721 |
| Gene Symbol: | MARCKS |
| Sub Type: | Phospho |
| UniProt Protein Function: | MARCKS: the most prominent cellular substrate of protein kinase C. Binds calmodulin, actin, and synapsin. A filamentous actin cross-linking protein. Critical for normal brain development. Phosphorylation by PKC displaces it from the plasma membrane, inhibiting F-actin cross-linking activity. Plays a role in growth cone adhesion: its nonphosphorylated form stabilizes integrin-mediated adhesions, and its phosphorylation-triggered release from adhesions causes localized growth cone detachment. Highly expressed in immature T and B lymphocytes: its expression is highest in CD4-8- T cells and B-cell blasts generated by antigen receptor signaling. Its expression and phosphorylation are closely linked to microglial activation processes involved in pathological conditions such as neuroinflammation and neurodegeneration. |
| UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; Actin-binding Chromosomal Location of Human Ortholog: 6q22.2 Cellular Component: actin cytoskeleton; cell cortex; centrosome; cytosol; dendritic spine; focal adhesion; germinal vesicle; growth cone; lysosome; microtubule; nerve terminal; outer dense fiber; plasma membrane Molecular Function:actin filament binding; calmodulin binding; phosphatidylserine binding; protein kinase C binding Biological Process: actin filament organization; brain development; cell-substrate adhesion; energy reserve metabolic process; intracellular protein transport; phospholipase D activation; regulation of insulin secretion |
| NCBI Summary: | The protein encoded by this gene is a substrate for protein kinase C. It is localized to the plasma membrane and is an actin filament crosslinking protein. Phosphorylation by protein kinase C or binding to calcium-calmodulin inhibits its association with actin and with the plasma membrane, leading to its presence in the cytoplasm. The protein is thought to be involved in cell motility, phagocytosis, membrane trafficking and mitogenesis. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P29966 |
| NCBI GenInfo Identifier: | 76803798 |
| NCBI Gene ID: | 4082 |
| NCBI Accession: | P29966.4 |
| UniProt Secondary Accession: | P29966,Q2LA83, Q5TDB7, E1P560, |
| UniProt Related Accession: | P29966 |
| Molecular Weight: | |
| NCBI Full Name: | Myristoylated alanine-rich C-kinase substrate |
| NCBI Synonym Full Names: | myristoylated alanine rich protein kinase C substrate |
| NCBI Official Symbol: | MARCKS |
| NCBI Official Synonym Symbols: | MACS; 80K-L; PKCSL; PRKCSL |
| NCBI Protein Information: | myristoylated alanine-rich C-kinase substrate |
| UniProt Protein Name: | Myristoylated alanine-rich C-kinase substrate |
| UniProt Synonym Protein Names: | Protein kinase C substrate, 80 kDa protein, light chain; 80K-L protein; PKCSL |
| Protein Family: | MARCKS-related protein |
| UniProt Gene Name: | MARCKS |
| UniProt Entry Name: | MARCS_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-MARCKS (Phospho-Ser158) Antibody, Anti-MARCKS 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.)
