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ClinMax™ Human Tumor Necrosis Factor Alpha (TNF-α) ELISA Kit

For research use only.

产品概述(Product Details)

ClinMax™ Human Tumor Necrosis Factor Alpha(TNF-α) ELISA Kit is a ready-to-use immunoassay kit, specifically designed to quantitate natural and recombinant human TNF-alpha that is present in biological samples, such as human serum, plasma, and cell culture supernatants. Our ClinMax™ ELISA Kit provides several benefits:

  1. Standards to calibrate with NIBSC/WHO standards for comparable results.
  2. Fully validation in biologic samples for detection range, sensitivity, inter- and intra-plate CV, recovery, dilution linearity, specificity, and matrix effects to ensure reliable results according to ICH M10 guideline.
  3. High-quality antibody pairs and protein standards, along with rigorous quality control, to guarantee consistent results across different batches.
  4. Simplified and straightforward protocols and ready-to-use reagents to save assay time.

应用说明(Application)

The kit is developed for quantitative detection of natural and recombinant human TNF-alpha in serum, plasma and cell culture supernatants.

It is for research use only.

流程图(Workflow)

TNF-alpha Workflow

关键信息(Key Features)

AnalyteTNF-α
Assay TypeSandwich-ELISA
ReactivityHuman
Sensitivity2.321 pg/mL
Range19.5 pg/mL-1250 pg/mL
Assay Time2 hr 50 min
Sample TypeCell Culture Supernatants, Plasma, Serum.
Sample volume100 μL
Format96-wells plate breakable into 12 x 8 wells strips

Elevate your research experience with our Cytokine/Biomarker Detection Kits, where accuracy, reliability, and ease of use are converging to deliver exceptional results.

存储(Storage)

Keep the unopened kit stored at 2-8 °C. Avoid using the kit beyond its expiration date. The opened kit should be stored per components table. The shelf life is 30 days from the date of opening.

质量管理控制体系(QMS)

  1. 质量管理体系(ISO, GMP)
  2. 质量优势
  3. 质控流程
 

典型数据-Typical Data Please refer to DS document for the assay protocol.

TNF-alpha TYPICAL DATA

For each experiment, a standard curve needs to be set for each microplate, and the specific OD value may vary depending on different laboratories, testers, or equipment. The following example data is for reference only. The sample concentration was calculated based on the results of the standard curve. The minimum detectable concentration of TNF-α is less than 2.321 pg/mL.

 

验证(Validation)

样本值(Sample Values)

Serum – Samples from apparently healthy volunteers were evaluated for the presence of human TNF-α in this assay. No medical histories were available for the donors used in this study.
Cell Culture Supernatant – Human peripheral blood mononuclear cells (PBMCs) were cultured and stimulated using CD28/OKT3 antibody then detected TNF-α secretion amount.

TNF-alpha SAMPLE VALUES

稀释线性(Dilution Linearity)

High concentrations (1200pg/mL) of human TNF-α were added to different diluted substrates for gradient dilution to evaluate the linearity of the assay.

TNF-alpha DILUTION LINEARITY

批内差异(Intra-Assay Statistics)

20 replicates of each of 3 samples containing different TNF-α concentrations were tested in one assay. Acceptable criteria: CV<15%.

TNF-alpha INTRA-ASSAY STATISTICS

批间差异(Inter-Assay Statistics)

3 samples containing 3 different concentrations of TNF-α were tested in independent assays. Acceptable criteria: CV<15%.

TNF-alpha INTER-ASSAY STATISTICS

回收率(Recovery)

TNF-α was spiked into 3 human serum samples, and then analyzed. The average recovery of TNF-α for serum samples is 101.0%, range is 89.6% - 111.4%.

TNF-alpha RECOVERY

 

组分(Materials Provided)

IDComponentsSize
CRS002-C01Pre-coated Anti-TNF-α Antibody Microplate1plate
CRS002-C02Human TNF-α Standard20μg
CRS002-C03Biotin-Anti-TNF-α Antibody20μg
CRS002-C04Streptavidin-HRP50 μL
CRS002-C0510xWashing Buffer 50 mL
CRS002-C062xDilution Buffer50 mL
CRS002-C07Substrate Solution12 mL
CRS002-C08Stop Solution7 mL

 
评论(3)
  1. 139XXXXXXX3
  2. 1人赞
  3. 最近开展的研究需要检测细胞培养上层中的 TNF-α,该试剂盒很好的满足需求,实验检测原理简单,操作便捷,节省了时间成本。
  4. 2023-11-22
  1. 176XXXXXXX8
  2. 0人赞
  3. 本次购买的ClinMax™ Human Tumor Necrosis Factor Alpha (TNF-α) ELISA Kit检测试剂盒用于检测细胞上清中TNFa的含量,此试剂盒为预制板,检测结果稳定,更方便、实验所需时间短,实验所需的样本量更少。
  4. >
  5. 2024-1-16
  1. 192XXXXXXX5
  2. 0人赞
  3. 我们是用来检测血清中TNF-Alpha的含量的,我们血清稀释50倍之后检测的,大大节约我们的珍贵样本,灵敏度很高。试剂盒我们还用来检测PBMC上清的含量,用途很多
  4. 2025-3-17
 
ACRO质量管理体系
 
 

前沿进展

Lactiplantibacillus plantarum FRT4 protects against fatty liver hemorrhage syndrome: regulating gut microbiota and FoxO/TLR-4/NF-κB signaling pathway in laying hens
Li, Meng, Liu et al
Microbiome (2025) 13 (1), 88
Abstract: Fatty liver hemorrhage syndrome (FLHS) has become one of the major factors leading to the death of laying hen in caged egg production. FLHS is commonly associated with lipid peroxidation, hepatocyte injury, decreased antioxidant capacity, and inflammation. However, there are limited evidences regarding the preventive effect of Lactiplantibacillus plantarum on FLHS in laying hens and its mechanisms. Our previous results showed that Lp. plantarum FRT4 alleviated FLHS by regulating lipid metabolism, but did not focus on its antioxidant and anti-inflammatory functions and mechanisms. Therefore, this study aimed to investigate the preventive mechanisms of Lp. plantarum FRT4 in alleviating FLHS, with a focus on its role in antioxidant activity and inflammation regulation.Supplementation with Lp. plantarum FRT4 enhanced the levels of T-AOC, T-SOD, and GSH-Px, while reducing the levels of TNF-α, IL-1β, IL-8, and NLRP3 in the liver and ovary of laying hens. Additionally, Lp. plantarum FRT4 upregulated the mRNA expressions of SOD1, SOD2, CAT, and GPX1, downregulated the mRNA expressions of pro-inflammatory factors IL-1β, IL-6, and NLRP3, and upregulated the mRNA expressions of anti-inflammatory factors IL-4 and IL-10. Lp. plantarum FRT4 improved the structure and metabolic functions of gut microbiota, and regulated the relative abundances of dominant phyla (Bacteroidetes, Firmicute, and Proteobacteria) and genera (Prevotella and Alistipes). Additionally, it influenced key KEGG pathways, including tryptophan metabolism, amino sugar and nucleotide sugar metabolism, insulin signaling pathway, FoxO signaling pathway. Spearman analysis revealed that the abundance of microbiota at different taxonomic levels was closely related to antioxidant enzymes and inflammatory factors. Furthermore, Lp. plantarum FRT4 modulated the mRNA expressions of related factors in the FoxO/TLR-4/NF-κB signaling pathway by regulating gut microbiota. Moreover, the levels of E2, FSH, and VTG were significantly increased in the ovary after Lp. plantarum FRT4 intervention.Lp. plantarum FRT4 effectively ameliorates FLHS in laying hens. This efficacy is attributed to its antioxidant and anti-inflammatory properties, which are mediated by modulating the structure and function of gut microbiota, and further intervening in the FoxO/TLR-4/NF-κB signaling pathway. These actions enhance hepatic and ovarian function and increase estrogen levels. Video Abstract.© 2025. The Author(s).
UVB-induced HaCat cell damage and Myricaria Paniculata's molecular effects
Liu, Ma, Chen et al
Sci Rep (2025) 15 (1), 10909
Abstract: The Qinghai‒Tibet Plateau, the "Roof of the World" in China, has high altitude, low pressure, thin air, little rain, long sunshine, and snow cover, causing 80-90% more Ultraviolet (UV) reflectance and greater skin UV exposure at high altitudes. Myricaria paniculata, a Tibetan plant growing at 2000-4500 m, has anti-inflammatory, antioxidant, and immune-boosting effects and can protect skin cells from Ultraviolet B (UVB)damage. The protective effects of Myricaria paniculata compounds against UVB-induced HaCat cell damage were explored. Samples were divided into normal, model, and treatment groups (seven compounds). First, the cell viability and apoptosis rates of each group were measured, along with the levels of factors such as Reactive oxygen species (ROS) and Superoxide dismutase (SOD). Network pharmacology analysis and molecular docking were subsequently performed. This study revealed that the compound enhanced cell survival, inhibited apoptosis, reduced ROS and Malondialdehyde (MDA) levels, and increased SOD activity. It also lowered the levels of Interleukin-6 (IL-6), Tumor Necrosis Factor-α (TNF-α), and Aspartate protein hydrolase 3 containing cysteine (Caspase-3). An analysis of the intersection between the 218 targets of the seven compounds found in Myricaria paniculata and the 1002 targets associated with skin inflammation revealed 59 common targets, with key targets including TNF and others. GO and KEGG analyses suggested the involvement of metabolic pathways. Seven core targets related to skin inflammation in Myricaria paniculata were identified by molecular docking. In addition, its compounds rhamnetin, rhamnocitrin, ferulic acid and kaempferol have good binding activity with TNF, PTGS2, EGFR and MMP9 targets. The Tibetan medicine Myricaria paniculata had a certain protective effect on UVB-induced HaCat cell damage.© 2025. The Author(s).
Diacerein's Antiproliferative Effects Alone and with 5-Fluorouracil in an Ehrlich Solid Tumour Model: Molecular Docking, Molecular Dynamics Simulation Studies, and Experimental Verification
Abdel-Maksoud, Altai, Albalawi et al
Eur J Pharmacol (2025)
Abstract: The current study used an experimental model of mammary gland carcinoma to assess the chemo-sensitizing effectiveness of the combined administration of diacerein and 5-Fluorouracil (5-FU). With docking scores of -8.1, -7.6, and -9.2 kcal/mol, respectively, the molecular docking experiments showed that diacerein exhibits significant binding affinities to Caspase-3, NF-κB, and AKT1. Molecular dynamics Simulations revealed that diacerein has favourable binding free energy (ΔGbind) of -26.7 kcal/mol for Caspase-3, -24.2 kcal/mol for NF-κB, and -39.9 kcal/mol for AKT1, combined with low root mean square deviation (RMSD) values of 3.1 Å, 1.6 Å, and 2.1 Å for the three targets respectively. To validate these findings in vivo, Ehrlich solid tumor (EST) was induced in female Swiss mice. Four groups of animals were randomly assigned: EST + vehicle, EST + 5-FU, EST + diacerein, and EST + combination. Diacerein and 5-FU combination treatment increased EST mice's life span and reduced the solid tumor's weight and volume. Furthermore, diacerein and 5-FU combination significantly suppressed oxidative stress, inhibited AKT phosphorylation, decreased downstream inflammation (NF-κB, TNF-α, IL-1β), and increased apoptosis by modulating Bax, Bcl2, P53, and caspase-3 levels in tumor tissues. In conclusion, by inhibiting the AKT/NF-κB axis, diacerein and 5-FU combination showed possible antiproliferative effectiveness in the EST model.Copyright © 2025. Published by Elsevier B.V.
Tri-network PVA/chitosan/gelatin hydrogel modified by tannic acid with self-healing, adhesive and anti-inflammatory properties to accelerate wound healing
Zhang, Li, Li et al
Int J Biol Macromol (2025)
Abstract: Wound inflammation is a key issue in wound healing as it often causes serious complications and delays wound healing. In this study, hemostatic and antimicrobial hydrogels composed of polyvinyl alcohol (PVA), chitosan (CS) and gelatin (Gel) were prepared. Phenylboronic acid (3-CPBA) and tannic acid (TA) were introduced to modify the multinetwork hydrogel to promote wound repair. PGCPT-1.2 hydrogel had a water content of >85 % and was biocompatible. Due to the antibacterial effect of chitosan itself. The PGCPT hydrogel exhibited 100 % antimicrobial activity against both Escherichia coli and Staphylococcus aureus within 12 h. The hydrogel exhibited shape memory behavior and self-healing ability. Histological analysis showed that PGCPT-1.2 hydrogel reduced tumor necrosis factor-α (TNF-α) levels by accelerating collagen deposition. The wound healing rate at day 14 was 97 % ± 0.4 %. PGCPT-1.2 hydrogel dressing with 1.2 % TA addition had the best effect in promoting wound healing, and it is a promising dressing for promoting wound healing and a therapeutic strategy worth developing.Copyright © 2025 Elsevier B.V. All rights reserved.
Showing 1-4 of 279851 papers.
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TNF-alpha靶点信息
英文全称:Tumor necrosis factor α
中文全称:肿瘤坏死因子α
种类:Homo sapiens
上市药物数量:64详情
临床药物数量:71详情
最高研发阶段:批准上市
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