Rat TNF-α(Tumor Necrosis Factor Alpha) ELISA Kit (E-EL-R2856)
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For research use only. Order now, ship in 3 days
Sensitivity | 9.38 pg/mL |
Detection Range | 15.63-1000 pg/mL |
Sample Volume | 100 μL |
Total Assay Time | 3 h 30 min |
Reacitivity | Rat |
Specificity | This kit recognizes Rat TNF-α in samples.No significant cross-reactivity or interference between Rat TNF-α and analogues was observed |
Recovery | 80%-120% |
Sample Type | Serum, plasma and other biological fluids |
Detection Method | Colorimetric method, ELISA, Sandwich |
Assay Type | Sandwich-ELISA |
Size | 96T / 48T / 24T / 96T*5 / 96T*10 |
Storage | 2-8℃ |
Expiration Date | 12 months |
Uniport ID | P16599 |
Research Area | Signal Transduction, Metabolism, Cancer, Immunology, Microbiology, Cardiovascular |
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1 Results
- HPB@LA@PDA nanoplatform ameliorates osteoarthritis by scavenging reactive oxygen species and remodelling the inflammatory microenvironment: An in vitro and in vivo study
IF:13.3
Journal:CHEMICAL ENGINEERING JOURNAL(2025)
DOI:10.1016/j.cej.2025.160592Reactivity:Rat
Sample Type:knee joint tissue
- Gut microbial dysbiosis exacerbates long-term cognitive impairments by promoting intestinal dysfunction and neuroinflammation following neonatal hypoxia-ischemia
IF:12.2
Journal:Gut Microbes(2025)
DOI:10.1080/19490976.2025.2471015Reactivity:Rat
Sample Type:serum
- Increased Alleviation of Bone Destruction in Individuals with Rheumatoid Arthritis via the Coinhibition of the METTL3 and YTHDF1 Axis by the Combination of Triptolide and Medicarpin
IF:10.1
Journal:Engineering(2025)
DOI:10.1016/j.eng.2025.03.014Reactivity:Rat
Sample Type:serum
- An injectable and adaptable system for the sustained release of hydrogen sulfide for targeted diabetic wound therapy by improving the microenvironment of inflammation regulation and angiogenesis
IF:9.4
Journal:Acta Biomaterialia(2025)
DOI:10.1016/j.actbio.2025.02.048Reactivity:Rat
Sample Type:Wound tissue
- Carboxybetaine modified chitosan as viscosupplementation for osteoarthritis therapy
IF:7.7
Journal:INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES(2025)
DOI:10.1016/j.ijbiomac.2025.142155Reactivity:Rat
Sample Type:serum
- Ubiquitin-specific protease 13 regulates FcεRI-mediated mast cell activation and allergic inflammation via SYK protein modulation
IF:7.7
Journal:INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES(2025)
DOI:10.1016/j.ijbiomac.2025.142302Reactivity:Rat
- Shuxuening injection improves myocardial injury after myocardial infarction by regulating macrophage polarization via the TLR4/NF-κB and PI3K/Akt signaling pathways
IF:6.7
Journal:PHYTOMEDICINE(2025)
DOI:10.1016/j.phymed.2025.156418Reactivity:Rat
Sample Type:Serum
- Parthenolide improves sepsis-induced coagulopathy by inhibiting mitochondrial-mediated apoptosis in vascular endothelial cells through BRD4/BCL-xL pathway
IF:6.1
Journal:Journal of Translational Medicine(2025)
DOI:10.1186/s12967-025-06114-0Reactivity:Rat
Sample Type:lung tissue
- MiR-370-3p regulate TLR4/SLC7A11/GPX4 to alleviate the progression of glucocorticoids-induced osteonecrosis of the femoral head by promoting osteogenesis and suppressing ferroptosis
IF:5.9
Journal:Journal of Orthopaedic Translation(2025)
DOI:10.1016/j.jot.2024.10.014Reactivity:Rat
Sample Type:serum
- Spatiotemporal Regulation of the Bone Immune Microenvironment via a ‘Zn2+–quercetin’ Hierarchical Delivery System for Bone Regeneration
IF:5.6
Journal:Regenerative Biomaterials(2025)
DOI:10.1093/rb/rbaf006Reactivity:Rat
Q1:Why is it necessary to add a protease inhibitor in tissue sample preparation during an Elisa experiment? Will it affect the detection significantly if there is no protease inhibitor?
Tissue samples may contain endogenous or exogenous proteases during processing, leading to degradation of extracted proteins. Therefore, it's necessary to add protease inhibitors during processing to ensure the integrity of target proteins. If customers can keep samples cold and handle them quickly during processing, omitting the protease inhibitor may not have a significant effect. After preparation, samples should be tested promptly or immediately aliquoted and frozen at -20°C or -80°C.
Q2:Which variant of the spike protein does this kit detect? Do you have a kit specific to detect the spike protein for the omicron variant?
This kit is designed for the original strain of the new crown virus, and the omicron variant has not been verified. However, we have verified 26 recombinant variants of the SARS-CoV-2 spike protein through the kit. For more information, customers can refer to the kit instructions (https://file.elabscience.com/Manual/covid_19/E-EL-E605 .pdf).
Q3:What is the range of enzyme activity of your IL-2 freeze-dried powder
Currently our freeze-dried powder is a concentration unit with no information on the activity unit for the time being.
Q4:What is the principle of adding stop solution to stop color reaction in ELISA experiment?
On the one hand, the activity of HRP enzyme is destroyed and the catalytic function of HRP enzyme is lost. On the other hand, the final color changes due to a change in pH.
Q5:The absorbance of the cell supernatant is less than that of the sample diluent alone, so how to concentrate the sample?
The amount of medium can be reduced for subsequent drug administration and modeling.
Q6:My sample volume is small. Can I reduce some reagents proportionally?
No, the detection system of our kits requires strict adherence to the specified sample volume to ensure accurate detection. If the sample volume is insufficient, consider diluting appropriately, but first conduct a pre-experiment to confirm the suitable dilution factor.
Q7:May I ask which type of plate to choose when ELISA testing?
According to the different bottom, it is divided into flat bottom, U-shaped bottom, V-shaped bottom and so on. The index of refraction of the flat bottom is low, which is suitable for detection in the enzyme reader. According to the color can be divided into transparent, black, white. Transparent is commonly used for the most general enzyme-linked immunoassay.
Q8:Is the TGF-β1 ELISA Kit detecting the active form of TGF-β1 or the precursor?
The active TGF-β dimer was detected
Q9:I need to measure corticosterone and testosterone in hair samples. Are there any suggested sample extraction methods?
Hair sample preparation method: Wash hair samples with methanol by adding 5 mL of HPLC-grade methanol to each sample, rotating for 3 minutes, then decanting excess methanol and rinsing hair twice. After washing, place the hair samples on aluminum foil, dry for 3 days in a protective cap. Weigh the dried hair samples and transfer them to 2ml polypropylene tubes containing stainless steel grinding beads. Place the tubes containing hair and beads in a bead beater, grind each sample for 2 minutes to produce powder. After grinding, add 1.5 mL of methanol to the tubes containing hair powder. Rotate samples slowly for 24 hours to extract steroids. Centrifuge at 10000 g for 4 minutes, transfer 0.6 mL of methanol supernatant containing steroids to new 1.5 mL microcentrifuge tubes. Dry the samples in a protective hood for 2-3 days to evaporate the methanol. Dilute the dried extract with 0.4 mL dilution buffer from the kit for detection.
Q10:I got nothing on the IL-18 standard
The standard product is placed in the reagent bottle and then freeze-dried. You can first centrifuge the reagent bottle with 10000×g for 1min, and then directly observe the bottom or side wall of the reagent bottle.