Rat PTGS2 / COX2 ELISA Kit
- SKU:
- RTFI00231
- Product Type:
- ELISA Kit
- Size:
- 96 Assays
- Uniprot:
- P35355
- Sensitivity:
- 75pg/ml
- Range:
- 125-8000pg/ml
- ELISA Type:
- Sandwich
- Synonyms:
- PTGS2, COX-2, Prostaglandin Endoperoxide Synthase 2, PGHS-2, PHS-II, PTGS2, cyclooxygenase 2b, cyclooxygenase-2, GRIPGHS, Cox-2, PGG, HS, PGH synthase 2, PHS II, PHS-2, prostaglandin G, H synthase 2, prostaglandin G, H synthase and cyclooxygenase, Pr
- Reactivity:
- Rat
- Research Area:
- Metabolism
Description
Rat PTGS2/COX2 ELISA Kit
The Rat PTGS2 (COX-2) ELISA Kit is a highly reliable and sensitive assay designed for the accurate quantification of PTGS2 (COX-2) levels in rat samples including serum, plasma, and cell culture supernatants. This kit offers exceptional specificity and precision, ensuring consistent and trustworthy results for a variety of research applications.PTGS2, also known as cyclooxygenase-2, is a key enzyme involved in the inflammatory response and is implicated in various diseases such as arthritis, cancer, and cardiovascular disorders.
By measuring PTGS2 levels, researchers can gain valuable insights into the pathophysiology of these conditions and identify potential therapeutic targets.Ideal for laboratories conducting studies on inflammation, pain, and cancer, the Rat PTGS2 (COX-2) ELISA Kit is a powerful tool for investigating the role of PTGS2 in disease progression and developing novel treatment strategies. Trust in the accuracy and sensitivity of this kit to advance your research efforts in the field of molecular biology and pharmacology.
| Product Name: | Rat PTGS2/COX-2 (Prostaglandin G/H synthase 2) ELISA Kit |
| Product Code: | RTFI00231 |
| Size: | 96 Assays |
| Target: | Rat PTGS2/COX-2 |
| Alias: | PTGS2, COX-2, Prostaglandin Endoperoxide Synthase 2, PGHS-2, PHS-II, PTGS2, cyclooxygenase 2b, cyclooxygenase-2, GRIPGHS, Cox-2, PGG, HS, PGH synthase 2, PHS II, PHS-2, prostaglandin G, H synthase 2, prostaglandin G, H synthase and cyclooxygenase, Prostaglandin H2 synthase 2, Prostaglandin-endoperoxide synthase 2 |
| Reactivity: | Rat |
| Detection Method: | Sandwich ELISA, Double Antibody |
| Sensitivity: | 75pg/ml |
| Range: | 125-8000pg/ml |
| Storage: | 4°C for 6 months |
| Note: | For Research Use Only |
| Recovery: | Matrices listed below were spiked with certain level of Rat PTGS2/COX-2 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat PTGS2/COX-2 in samples. | ||||||||||||||||
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| Linearity: | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat PTGS2/COX-2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected. | ||||||||||||||||
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| Intra-Assay: | CV <8% | ||||||||||||||||
| Inter-Assay: | CV <10% |
| Uniprot: | P35355 |
| UniProt Protein Function: | COX-2: Mediates the formation of prostaglandins from arachidonate. May have a role as a major mediator of inflammation and/or a role for prostanoid signaling in activity-dependent plasticity. Homodimer. Belongs to the prostaglandin G/H synthase family. |
| UniProt Protein Details: | Protein type:EC 1.14.99.1; Lipid Metabolism - arachidonic acid; Oxidoreductase Chromosomal Location of Human Ortholog: 13q21 Cellular Component: caveola; cytoplasm; endoplasmic reticulum; neuron projection; nucleus; protein complex Molecular Function:enzyme binding; heme binding; lipid binding; oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen; prostaglandin-endoperoxide synthase activity; protein binding; protein homodimerization activity Biological Process: aging; angiogenesis; bone mineralization; brown fat cell differentiation; cyclooxygenase pathway; decidualization; embryo implantation; hair cycle; inflammatory response; learning; memory; negative regulation of apoptosis; negative regulation of calcium ion transport; negative regulation of caspase activity; negative regulation of cell cycle; negative regulation of cell proliferation; negative regulation of smooth muscle contraction; negative regulation of synaptic transmission, dopaminergic; ovulation; positive regulation of apoptosis; positive regulation of cell proliferation; positive regulation of fever; positive regulation of NF-kappaB import into nucleus; positive regulation of nitric oxide biosynthetic process; positive regulation of peptidyl-serine phosphorylation; positive regulation of prostaglandin biosynthetic process; positive regulation of smooth muscle cell proliferation; positive regulation of smooth muscle contraction; positive regulation of synaptic plasticity; positive regulation of synaptic transmission, glutamatergic; positive regulation of vasoconstriction; prostaglandin biosynthetic process; regulation of blood pressure; regulation of cell proliferation; response to cytokine stimulus; response to drug; response to estradiol stimulus; response to fructose stimulus; response to glucocorticoid stimulus; response to lipopolysaccharide; response to lithium ion; response to manganese ion; response to organic cyclic substance; response to organic nitrogen; response to organic substance; response to radiation; response to vitamin D; sensory perception of pain |
| UniProt Code: | P35355 |
| NCBI GenInfo Identifier: | 148747270 |
| NCBI Gene ID: | 29527 |
| NCBI Accession: | NP_058928.3 |
| UniProt Secondary Accession: | P35355,Q64379, Q925V4, |
| Molecular Weight: | 69,164 Da |
| NCBI Full Name: | prostaglandin G/H synthase 2 |
| UniProt Protein Name: | Prostaglandin G/H synthase 2 |
| UniProt Synonym Protein Names: | Cyclooxygenase-2; COX-2; PHS II; Prostaglandin H2 synthase 2; PGH synthase 2; PGHS-2; Prostaglandin-endoperoxide synthase 2 |
| Protein Family: | Prostaglandin G/H synthase |
| UniProt Gene Name: | Ptgs2Â Â |
| Step | Procedure |
| 1. | Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells! |
| 2. | Aliquot 0.1ml standard solutions into the standard wells. |
| 3. | Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well. |
| 4. | Add 0.1 ml of properly diluted sample ( Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells. |
| 5. | Seal the plate with a cover and incubate at 37°C for 90 min. |
| 6. | Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2. |
| 7. | Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall. |
| 8. | Seal the plate with a cover and incubate at 37°C for 60 min. |
| 9. | Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash. |
| 10. | Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min. |
| 11. | Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min. |
| 12. | Add 90 µL of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color. |
| 13. | Add 50 µL of Stop solution into each well and mix thoroughly. The color changes into yellow immediately. |
| 14. | Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution. |
When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.
| Sample Type | Protocol |
| Serum: | If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. If serum separator tubes are not being used, allow samples to clotovernight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Removeserum and assay promptly or aliquot and store the samples at-80°C. Avoid multiple freeze-thaw cycles. |
| Plasma: | Collect plasma using EDTA or heparin as an anti-coagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.Note: Over haemolysed samples are not suitable for use with this kit. |
| Urine & Cerebrospinal Fluid: | Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid. |
| Cell Culture Supernatant: | Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately. |
| Cell Lysates: | Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20°C. |
| Tissue Homogenates: | The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenizein 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or-80°C. |
| Tissue Lysates: | Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C. |
| Breast Milk: | Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles. |
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