MSK1 (Phospho-Ser212) Colorimetric Cell-Based ELISA Kit

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SKU:
CBCAB00496
Product Type:
ELISA Kit
ELISA Type:
Cell Based Phospho Specific
Research Area:
Immunology
Reactivity:
Human
Mouse
Detection Method:
Colorimetric
Frequently bought together:

Description

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MSK1 (Phospho-Ser212)Colorimetric Cell-Based ELISA Kit

The MSK1 Phospho-Ser212 Colorimetric Cell-Based ELISA Kit is a highly sensitive and specific assay designed for the accurate quantification of phosphorylated MSK1 (Mitogen- and Stress-Activated Protein Kinase 1) at serine 212 in cell lysates. This kit enables researchers to study the regulation of MSK1 activity in various cellular processes, such as cell proliferation, differentiation, and stress response.MSK1 is a key signaling molecule that plays a crucial role in cellular functions, including gene expression, cell cycle progression, and immune response. Phosphorylation of MSK1 at serine 212 is known to be essential for its kinase activity and downstream signaling pathways.

Dysregulation of MSK1 activity has been implicated in various diseases, including cancer, inflammation, and neurodegenerative disorders, highlighting the importance of studying its phosphorylation status.The MSK1 Phospho-Ser212 Colorimetric Cell-Based ELISA Kit provides a simple and reliable method for measuring phosphorylated MSK1 levels in cell lysates, allowing researchers to investigate the role of MSK1 signaling in different pathophysiological conditions. With its high sensitivity and specificity, this kit is an essential tool for advancing research in cell biology, signal transduction, and drug discovery.

Product Name:MSK1 (Phospho-Ser212) Colorimetric Cell-Based ELISA
Product Code:CBCAB00496
ELISA Type:Cell-Based
Target:MSK1 (Phospho-Ser212)
Reactivity:Human, Mouse
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nm
Format:2 x 96-Well Microplates

The MSK1 (Phospho-Ser212) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect MSK1 protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated MSK1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on MSK1 phosphorylation.

Qualitative determination of MSK1 (Phospho-Ser212) concentration is achieved by an indirect ELISA format. In essence, MSK1 (Phospho-Ser212) is captured by MSK1 (Phospho-Ser212)-specific primary antibodies while the HRP-conjugated secondary antibodies bind the Fc region of the primary antibody. Through this binding, the HRP enzyme conjugated to the secondary 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: 9252, UniProt ID: O75582, OMIM: 603607, Unigene: Hs.510225
Gene Symbol:RPS6KA5
Sub Type:Phospho
UniProt Protein Function:MSK1: an AGC kinase of the RSK family. Has two kinase domains connected by a regulatory linker region. Enzyme activity requires the presence of both kinase domains. Is phosphorylated and activated by Erk as well as p38 MAPK in response to growth factors and cellular stress.
UniProt Protein Details:

Protein type:EC 2.7.11.1; Protein kinase, AGC; Kinase, protein; Protein kinase, Ser/Thr (non-receptor); AGC group; RSK family; MSK subfamily

Chromosomal Location of Human Ortholog: 14q31-q32.1

Cellular Component: cytoplasm; nucleoplasm; nucleus

Molecular Function:ATP binding; histone serine kinase activity (H3-S10 specific); magnesium ion binding; protein binding; protein kinase activity; protein serine/threonine kinase activity

Biological Process: activation of CREB transcription factor; activation of NF-kappaB transcription factor; axon guidance; epidermal growth factor receptor signaling pathway; histone phosphorylation; inflammatory response; innate immune response; MyD88-dependent toll-like receptor signaling pathway; MyD88-independent toll-like receptor signaling pathway; negative regulation of cytokine production; negative regulation of transcription, DNA-dependent; nerve growth factor receptor signaling pathway; positive regulation of histone acetylation; positive regulation of histone phosphorylation; positive regulation of transcription from RNA polymerase II promoter; protein amino acid phosphorylation; regulation of transcription, DNA-dependent; stimulatory C-type lectin receptor signaling pathway; stress-activated MAPK cascade; toll-like receptor 10 signaling pathway; toll-like receptor 2 signaling pathway; toll-like receptor 3 signaling pathway; toll-like receptor 4 signaling pathway; toll-like receptor 5 signaling pathway; toll-like receptor 9 signaling pathway; toll-like receptor signaling pathway

UniProt Code:O75582
NCBI GenInfo Identifier:37999482
NCBI Gene ID:9252
NCBI Accession:O75582.1
UniProt Secondary Accession:O75582,O95316, Q96AF7, B7Z2Y5,
UniProt Related Accession:O75582
Molecular Weight:81,780 Da
NCBI Full Name:Ribosomal protein S6 kinase alpha-5
NCBI Synonym Full Names:ribosomal protein S6 kinase A5
NCBI Official Symbol:RPS6KA5  
NCBI Official Synonym Symbols:MSK1; RLPK; MSPK1  
NCBI Protein Information:ribosomal protein S6 kinase alpha-5
UniProt Protein Name:Ribosomal protein S6 kinase alpha-5
UniProt Synonym Protein Names:90 kDa ribosomal protein S6 kinase 5; Nuclear mitogen- and stress-activated protein kinase 1; RSK-like protein kinase; RSKL
Protein Family:Ribosomal protein S6 kinase
UniProt Gene Name:RPS6KA5  
UniProt Entry Name:KS6A5_HUMAN
ComponentQuantity
96-Well Cell Culture Clear-Bottom Microplate2 plates
10X TBS24 mL
Quenching Buffer24 mL
Blocking Buffer50 mL
15X Wash Buffer50 mL
Primary Antibody Diluent12 mL
100x Anti-Phospho Target Antibody 60 µL
100x Anti-Target Antibody60 µL
Anti-GAPDH Antibody60 µL
HRP-Conjugated Anti-Rabbit IgG Antibody12 mL
HRP-Conjugated Anti-Mouse IgG Antibody12 mL
SDS Solution12 mL
Stop Solution24 mL
Ready-to-Use Substrate12 mL
Crystal Violet Solution12 mL
Adhesive Plate Seals2 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.

StepProcedure
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-MSK1 (Phospho-Ser212) Antibody, Anti-MSK1 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.)

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