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Moesin/Ezrin/Radixin (Phospho-Thr558) Colorimetric Cell-Based ELISA Kit

SKU:
CBCAB01462
Product Type:
ELISA Kit
ELISA Type:
Cell Based Phospho Specific
Research Area:
Immunology
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
$719
Frequently bought together:

Description

system_update_altDatasheetMSDS

Moesin/Ezrin/Radixin (Phospho-Thr558)Colorimetric Cell-Based ELISA Kit

The Moesin/Ezrin/Radixin Phospho Thr558 Colorimetric Cell-Based ELISA Kit is a cutting-edge tool designed for the accurate measurement of phosphorylated forms of Moesin, Ezrin, and Radixin at threonine 558 in cell lysates. This kit offers high sensitivity and specificity, ensuring precise and consistent results for a wide range of research applications.Moesin, Ezrin, and Radixin are key regulatory proteins involved in the organization of the cytoskeleton and cell membrane dynamics. Phosphorylation at threonine 558 plays a crucial role in their function, impacting processes such as cell adhesion, migration, and signal transduction. Dysregulation of these proteins has been implicated in various diseases, including cancer, inflammation, and metastasis, highlighting their importance as potential therapeutic targets.

By accurately quantifying phosphorylated Moesin, Ezrin, and Radixin at threonine 558, researchers can gain valuable insights into cellular signaling pathways and disease mechanisms, ultimately leading to the development of novel diagnostic tools and therapeutic interventions. The Moesin/Ezrin/Radixin Phospho Thr558 Colorimetric Cell-Based ELISA Kit is a valuable asset for any laboratory conducting research in cell biology, cancer biology, or drug development.

Product Name:Moesin/Ezrin/Radixin (Phospho-Thr558) Colorimetric Cell-Based ELISA
Product Code:CBCAB01462
ELISA Type:Cell-Based
Target:Moesin/Ezrin/Radixin (Phospho-Thr558)
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nm
Format:2 x 96-Well Microplates

The Moesin/Ezrin/Radixin (Phospho-Thr558) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect Moesin/Ezrin/Radixin protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated Moesin/Ezrin/Radixin in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on Moesin/Ezrin/Radixin phosphorylation.

Qualitative determination of Moesin/Ezrin/Radixin (Phospho-Thr558) concentration is achieved by an indirect ELISA format. In essence, Moesin/Ezrin/Radixin (Phospho-Thr558) is captured by Moesin/Ezrin/Radixin (Phospho-Thr558)-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: 4478/5962, UniProt ID: P26038/P35241/P15311, OMIM: 309845/179410/611022, Unigene: Hs.81328/Hs.263671/Hs.592679
Gene Symbol:MSN
Sub Type:Phospho
UniProt Protein Function:Probably involved in connections of major cytoskeletal structures to the plasma membrane. May inhibit herpes simplex virus 1 infection at an early stage.
NCBI Summary:Moesin (for membrane-organizing extension spike protein) is a member of the ERM family which includes ezrin and radixin. ERM proteins appear to function as cross-linkers between plasma membranes and actin-based cytoskeletons. Moesin is localized to filopodia and other membranous protrusions that are important for cell-cell recognition and signaling and for cell movement. [provided by RefSeq, Jul 2008]
UniProt Code:P26038
NCBI GenInfo Identifier:127234
NCBI Gene ID:4478
NCBI Accession:P26038.3
UniProt Secondary Accession:P26038,P35241, P15311, P26041, P26043, P26040, O35763 P31977,
UniProt Related Accession:P26038
Molecular Weight:67,820 Da
NCBI Full Name:Moesin
NCBI Synonym Full Names:moesin
NCBI Official Symbol:MSN  
NCBI Official Synonym Symbols:HEL70  
NCBI Protein Information:moesin
UniProt Protein Name:Moesin
UniProt Synonym Protein Names:Membrane-organizing extension spike protein
UniProt Gene Name:MSN  
UniProt Entry Name:MOES_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-Moesin/Ezrin/Radixin (Phospho-Thr558) Antibody, Anti-Moesin/Ezrin/Radixin 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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