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Cytochrome P450 2C8/9/18/19 Colorimetric Cell-Based ELISA

SKU:
CBCAB01191
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Reactivity:
Human
Detection Method:
Colorimetric
€599
Frequently bought together:

Description

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Cytochrome P450 2C8/9/18/19 Colorimetric Cell-Based ELISA

The Cytochrome P450 2C8/9/18/19 Colorimetric Cell-based ELISA Kit from Assay Genie is a powerful tool for researchers looking to accurately detect and quantify the levels of cytochrome P450 2C8, 2C9, 2C18, and 2C19 in cell lysates, serum, and other biological samples. This kit offers high sensitivity and specificity, providing reliable and precise results for a variety of research applications.Cytochrome P450 enzymes are important in drug metabolism and have implications in various diseases and drug interactions.

Understanding the activity of these enzymes can help in personalized medicine approaches and drug development.With the Cytochrome P450 2C8/9/18/19 Colorimetric Cell-based ELISA Kit, researchers can confidently study the function and expression of these key enzymes, leading to valuable insights into drug metabolism and disease mechanisms. Upgrade your research capabilities with this advanced ELISA kit from Assay Genie.

Product Name:Cytochrome P450 2C8/9/18/19 Colorimetric Cell-Based ELISA
Product Code:CBCAB01191
ELISA Type:Cell-Based
Target:Cytochrome P450 2C8/9/18/19
Reactivity:Human
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The Cytochrome P450 2C8/9/18/19 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect Cytochrome P450 2C8/9/18/19 protein expression profile in cells. The kit can be used for measuring the relative amounts of Cytochrome P450 2C8/9/18/19 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on Cytochrome P450 2C8/9/18/19.

Qualitative determination of Cytochrome P450 2C8/9/18/19 concentration is achieved by an indirect ELISA format. In essence, Cytochrome P450 2C8/9/18/19 is captured by Cytochrome P450 2C8/9/18/19-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: 1562/1558/1559/1557, UniProt ID: P33260/P10632/P11712/P33261, OMIM: 601131/601129/601130/124020, Unigene: Hs.511872/Hs.709188/Hs.282624/Hs.282409
Gene Symbol:CYP2C8/9/18/19
Sub Type:None
UniProt Protein Function:CYP2C18: a member of the cytochrome P450 superfamily of enzymes. Cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. Participates in the oxidation of a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Localizes to the endoplasmic reticulum but its specific substrate has not yet been determined. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24.
UniProt Protein Details:

Protein type:Cofactor and Vitamin Metabolism - retinol; Xenobiotic Metabolism - metabolism by cytochrome P450; EC 1.14.14.1; Oxidoreductase; Xenobiotic Metabolism - drug metabolism - cytochrome P450; Lipid Metabolism - arachidonic acid; Lipid Metabolism - linoleic acid

Chromosomal Location of Human Ortholog: 10q24

Cellular Component: endoplasmic reticulum membrane

Molecular Function:arachidonic acid epoxygenase activity; monooxygenase activity; oxygen binding; steroid hydroxylase activity

Biological Process: epoxygenase P450 pathway; xenobiotic metabolic process

NCBI Summary:This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum but its specific substrate has not yet been determined. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. An additional gene, CYP2C17, was once thought to exist; however, CYP2C17 is now considered an artefact based on a chimera of CYP2C18 and CYP2C19. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Code:P33260
NCBI GenInfo Identifier:67476954
NCBI Gene ID:1562
NCBI Accession:P33260.3
UniProt Secondary Accession:P33260,Q16703, Q16751, Q4VAT5, Q6GRG1, B2R8K2,
UniProt Related Accession:P33260
Molecular Weight:48,805 Da
NCBI Full Name:Cytochrome P450 2C18
NCBI Synonym Full Names:cytochrome P450 family 2 subfamily C member 18
NCBI Official Symbol:CYP2C18  
NCBI Official Synonym Symbols:CPCI; CYP2C; CYP2C17; P450IIC17; P450-6B/29C  
NCBI Protein Information:cytochrome P450 2C18
UniProt Protein Name:Cytochrome P450 2C18
UniProt Synonym Protein Names:CYPIIC18; Cytochrome P450-6b/29c
Protein Family:Cytochrome
UniProt Gene Name:CYP2C18  
UniProt Entry Name:CP2CI_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-Cytochrome P450 2C8/9/18/19 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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