WEE1 (Phospho-Ser642) Colorimetric Cell-Based ELISA Kit

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SKU:
CBCAB01479
Product Type:
ELISA Kit
ELISA Type:
Cell Based Phospho Specific
Research Area:
Cell Cycle
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
Frequently bought together:

Description

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WEE1 (Phospho-Ser642)Colorimetric Cell-Based ELISA Kit

The WEE1 Phospho-Ser642 Colorimetric Cell-Based ELISA Kit is a reliable and sensitive tool for measuring levels of phosphorylated WEE1 protein in cell lysates. WEE1 is a key regulator of cell cycle progression and checkpoint control, making it a valuable target for cancer research and drug development.This ELISA kit offers accurate and reproducible results, allowing researchers to study the role of WEE1 in cell cycle regulation and potential therapeutic strategies.

By detecting phosphorylated WEE1 levels, this kit provides valuable insights into the mechanisms of cancer development and progression.Overall, the WEE1 Phospho-Ser642 Colorimetric Cell-Based ELISA Kit is an essential tool for studying WEE1 signaling pathways and identifying potential targets for novel cancer therapies.

Product Name:WEE1 (Phospho-Ser642) Colorimetric Cell-Based ELISA
Product Code:CBCAB01479
ELISA Type:Cell-Based
Target:WEE1 (Phospho-Ser642)
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nm
Format:2 x 96-Well Microplates

The WEE1 (Phospho-Ser642) Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect WEE1 protein phosphorylation and expression profile in cells. The kit can be used for measuring the relative amounts of phosphorylated WEE1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie. siRNA or chemicals), or activators have on WEE1 phosphorylation.

Qualitative determination of WEE1 (Phospho-Ser642) concentration is achieved by an indirect ELISA format. In essence, WEE1 (Phospho-Ser642) is captured by WEE1 (Phospho-Ser642)-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: 7465, UniProt ID: P30291, OMIM: 193525, Unigene: Hs.249441
Gene Symbol:WEE1
Sub Type:Phospho
UniProt Protein Function:Wee1: a protein kinase of the WEE family. A nuclear protein which catalyzes the inhibitory tyrosine phosphorylation of CDC2/cyclin B kinase, and appears to coordinate the transition between DNA replication and mitosis by protecting the nucleus from cytoplasmically activated CDC2 kinase.
UniProt Protein Details:

Protein type:EC 2.7.10.2; Kinase, protein; Protein kinase, Ser/Thr (non-receptor); Protein kinase, Other; Other group; WEE family

Chromosomal Location of Human Ortholog: 11p15.4

Cellular Component: nucleolus; nucleoplasm; nucleus

Molecular Function:kinase activity; protein binding; protein-tyrosine kinase activity

Biological Process: G2/M transition of mitotic cell cycle; regulation of cell cycle

NCBI Summary:This gene encodes a nuclear protein, which is a tyrosine kinase belonging to the Ser/Thr family of protein kinases. This protein catalyzes the inhibitory tyrosine phosphorylation of CDC2/cyclin B kinase, and appears to coordinate the transition between DNA replication and mitosis by protecting the nucleus from cytoplasmically activated CDC2 kinase. [provided by RefSeq, Jul 2008]
UniProt Code:P30291
NCBI GenInfo Identifier:1351419
NCBI Gene ID:7465
NCBI Accession:P30291.2
UniProt Secondary Accession:P30291,B3KVE1, D3DQV0,
UniProt Related Accession:P30291
Molecular Weight:49,072 Da
NCBI Full Name:Wee1-like protein kinase
NCBI Synonym Full Names:WEE1 G2 checkpoint kinase
NCBI Official Symbol:WEE1  
NCBI Official Synonym Symbols:WEE1A; WEE1hu  
NCBI Protein Information:wee1-like protein kinase
UniProt Protein Name:Wee1-like protein kinase
UniProt Synonym Protein Names:Wee1A kinase
Protein Family:Wee1-like protein kinase
UniProt Gene Name:WEE1  
UniProt Entry Name:WEE1_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-WEE1 (Phospho-Ser642) Antibody, Anti-WEE1 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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