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OXSR1 Colorimetric Cell-Based ELISA Kit

SKU:
CBCAB00787
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Reactivity:
Human
Mouse
Detection Method:
Colorimetric
€599
Frequently bought together:

Description

system_update_altDatasheetMSDS

OXSR1 Colorimetric Cell-Based ELISA Kit

The OXSR1 Colorimetric Cell-Based ELISA Kit from Assay Genie is a cutting-edge tool designed for the precise measurement of OXSR1 (oxidative stress responsive kinase 1) levels in cell lysates and tissue homogenates. This innovative kit utilizes a colorimetric assay method, providing high sensitivity and accuracy for reliable and reproducible results.OXSR1 is a crucial kinase involved in cellular responses to oxidative stress, playing a vital role in regulating cell survival and apoptosis. Dysregulation of OXSR1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and cardiovascular diseases, making it a valuable biomarker for understanding disease mechanisms and developing targeted therapies.

With the OXSR1 Colorimetric Cell-Based ELISA Kit, researchers can easily and effectively quantify OXSR1 levels in their samples, enabling comprehensive studies on oxidative stress-related pathways and potential therapeutic interventions. Invest in this advanced kit today to accelerate your research and contribute to scientific advancements in the field of cellular biology.

Product Name:OXSR1 Colorimetric Cell-Based ELISA
Product Code:CBCAB00787
ELISA Type:Cell-Based
Target:OXSR1
Reactivity:Human, Mouse
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The OXSR1 Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect OXSR1 protein expression profile in cells. The kit can be used for measuring the relative amounts of OXSR1 in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on OXSR1.

Qualitative determination of OXSR1 concentration is achieved by an indirect ELISA format. In essence, OXSR1 is captured by OXSR1-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: 9943, UniProt ID: O95747, OMIM: 604046, Unigene: Hs.475970
Gene Symbol:OXSR1
Sub Type:None
UniProt Protein Function:Regulates downstream kinases in response to environmental stress. May also have a function in regulating the actin cytoskeleton.
NCBI Summary:The product of this gene belongs to the Ser/Thr protein kinase family of proteins. It regulates downstream kinases in response to environmental stress, and may play a role in regulating the actin cytoskeleton. [provided by RefSeq, Jul 2008]
UniProt Code:O95747
NCBI GenInfo Identifier:4826878
NCBI Gene ID:9943
NCBI Accession:NP_005100.1
UniProt Secondary Accession:O95747,Q3LR53, Q7Z501, Q9UPQ1,
UniProt Related Accession:O95747
Molecular Weight:58,022 Da
NCBI Full Name:serine/threonine-protein kinase OSR1
NCBI Synonym Full Names:oxidative stress responsive 1
NCBI Official Symbol:OXSR1  
NCBI Official Synonym Symbols:OSR1  
NCBI Protein Information:serine/threonine-protein kinase OSR1
UniProt Protein Name:Serine/threonine-protein kinase OSR1
UniProt Synonym Protein Names:Oxidative stress-responsive 1 protein
Protein Family:Protein odd-skipped
UniProt Gene Name:OXSR1  
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-OXSR1 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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