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Cytochrome P450 2U1 Colorimetric Cell-Based ELISA

SKU:
CBCAB01195
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
€599
Frequently bought together:

Description

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Cytochrome P450 2U1 Colorimetric Cell-Based ELISA

The Cytochrome P450 2U1 Colorimetric Cell-Based ELISA kit from AssayGenie is a powerful tool for researchers looking to accurately quantify the levels of this important enzyme in cell culture supernatants and tissue samples. This kit offers high sensitivity and specificity, allowing for reliable and reproducible results that can support a wide range of research applications.Cytochrome P450 2U1 is a key enzyme involved in drug metabolism and detoxification processes in the body, and abnormalities in its function have been linked to various diseases and drug interactions.

By accurately measuring the levels of Cytochrome P450 2U1, researchers can gain valuable insights into these processes and potentially identify new therapeutic targets.Overall, the Cytochrome P450 2U1 Colorimetric Cell-Based ELISA kit is an essential tool for researchers studying drug metabolism, toxicology, and related fields, offering a reliable and efficient way to quantitatively analyze Cytochrome P450 2U1 levels in a variety of biological samples.

Product Name:Cytochrome P450 2U1 Colorimetric Cell-Based ELISA
Product Code:CBCAB01195
ELISA Type:Cell-Based
Target:Cytochrome P450 2U1
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The Cytochrome P450 2U1 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect Cytochrome P450 2U1 protein expression profile in cells. The kit can be used for measuring the relative amounts of Cytochrome P450 2U1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on Cytochrome P450 2U1.

Qualitative determination of Cytochrome P450 2U1 concentration is achieved by an indirect ELISA format. In essence, Cytochrome P450 2U1 is captured by Cytochrome P450 2U1-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: 113612, UniProt ID: Q7Z449, OMIM: 610670, Unigene: Hs.109087
Gene Symbol:CYP2U1
Sub Type:None
UniProt Protein Function:CYP2U1: Catalyzes the hydroxylation of arachidonic acid, docosahexaenoic acid and other long chain fatty acids. May modulate the arachidonic acid signaling pathway and play a role in other fatty acid signaling processes. Belongs to the cytochrome P450 family. 2 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Membrane protein, multi-pass; Oxidoreductase; Membrane protein, integral; EC 1.14.14.1; Lipid Metabolism - arachidonic acid

Chromosomal Location of Human Ortholog: 4q25

Cellular Component: endoplasmic reticulum membrane; intracellular membrane-bound organelle; cytoplasm; integral to membrane

Molecular Function:iron ion binding; heme binding; oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen; steroid hydroxylase activity; oxygen binding

Biological Process: organic acid metabolic process; xenobiotic metabolic process; exogenous drug catabolic process; arachidonic acid metabolic process

Disease: Spastic Paraplegia 56, Autosomal Recessive

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 enzyme is a hydroxylase that metabolizes arachidonic acid, docosahexaenoic acid, and other long chain fatty acids. [provided by RefSeq, Jul 2008]
UniProt Code:Q7Z449
NCBI GenInfo Identifier:74762432
NCBI Gene ID:113612
NCBI Accession:Q7Z449.1
UniProt Secondary Accession:Q7Z449,Q96EQ6, B2RMV7,
UniProt Related Accession:Q7Z449
Molecular Weight:18,578 Da
NCBI Full Name:Cytochrome P450 2U1
NCBI Synonym Full Names:cytochrome P450, family 2, subfamily U, polypeptide 1
NCBI Official Symbol:CYP2U1  
NCBI Official Synonym Symbols:SPG49; SPG56; P450TEC  
NCBI Protein Information:cytochrome P450 2U1; spastic paraplegia 49
UniProt Protein Name:Cytochrome P450 2U1
Protein Family:Cytochrome
UniProt Gene Name:CYP2U1  
UniProt Entry Name:CP2U1_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 2U1 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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