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Rat TNF-α ELISA kit

Product#: CS-CSB-E11987r-IS
$796.32
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Low Signal Optimization Reagents

4 core reagents below are included with every order, plus 1 of the 2 detection-specific reagents (matched automatically to your kit type) — 5 components, every time.

DCP-PIC100X

Protease Inhibitor Cocktail (100X)

Included with every order
 DCP-SM1AbTBS1X

SigMax 1Ab-TBS

Included with every order
 DCP-UTBS1X

Universal Blocking Buffer

Included with every order
 DCP-SM2AbTBS1X

SigMax 2Ab-TBS

Included with every order

+ the 5th component, matched to your kit's detection method:

DCP-HRPTBS1X

HRPQuench-TBS

Exclusively for HRP-based kits
OR
DCP-ALPTBS1X

ALPQuench-TBS

Exclusively for ALP-based kits

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Rat ELISA Kit · Immunology

Rat TNF-α ELISA kit

Sandwich quantitative immunoassay for Rat TNF-α ELISA kit in rat tissue homogenates, cell culture supernates, bronchoalveolar lavage fluid  available in multiple catalog sizes:

Trial 24T 96T

Note: Please send inquiries regarding Trial 24T orders to support@diagnocine.com.

Detection Range
15.6-1,000 pg/mL
Sensitivity
3.9 pg/mL
Assay Time
1-5 hours
Sample Volume
50-100 μL
Product specifications
Uniprot No.P16599
SpeciesRattus norvegicus (Rat)
Sample typestissue homogenates, cell culture supernates, bronchoalveolar lavage fluid
Detection range15.6 pg/mL-1000 pg/mL
Sensitivity3.9 pg/mL
Assay time1-5h
Sample loading volume50-100μL
Detection wavelength450 nm
Assay principleSandwich (Quantitative)
Data analysisStandard curve + Curve Expert software
Research areaImmunology
Storage condition2-8°C (see protocol for full details)
Shipping condition4 °C
Shelf life6 months
Rat TNF-α ELISA kit tissue homogenates cell culture supernates bronchoalveolar lavage fluid Immunology Rat ELISA
Lead Time

10 business days

Processing + 3-5 days shipping

Availability

In Stock : USA

Worldwide shipping available

Assay principle
Sample prep
Antibody capture
450 nm detection
Standard curve
Quantification

In this sandwich ELISA, Rat TNF-α ELISA kit in the sample is captured between a pre-coated capture antibody and a detection antibody. Signal intensity is proportional to analyte concentration. Quantification uses a standard curve fitted with Curve Expert software, covering 15.6 pg/mL-1000 pg/mL with a minimum detectable dose of 3.9 pg/mL.

For research use only (RUO). Not intended for diagnostic or therapeutic purposes. Validated in rat tissue homogenates, cell culture supernates, bronchoalveolar lavage fluid matrices only.
Description

This ELISA kit provides quantitative measurement of TNF (tumor necrosis factor) in Rattus norvegicus samples, supporting immunology research focused on innate immune activation and inflammatory signaling. Because TNF is a rapidly induced, short-lived cytokine whose concentrations can vary dramatically between baseline and inflammatory states, this kit is designed to capture that full dynamic window across multiple sample contexts.

Detection Range: The 15.6–1000 pg/mL range spans from near-baseline circulating TNF levels in unstimulated rat tissues to the elevated concentrations observed in LPS-challenged or sepsis-model animals, minimizing the need for serial dilutions while covering both resting and acutely inflamed conditions.

Alternative Names
Tnf ELISA Kit; Tnfa ELISA Kit; Tnfsf2 ELISA Kit; Tumor necrosis factor ELISA Kit; Cachectin ELISA Kit; TNF-alpha ELISA Kit; Tumor necrosis factor ligand superfamily member 2 ELISA Kit; TNF-a) [Cleaved into: Tumor necrosis factor ELISA Kit; membrane form ELISA Kit; N-terminal fragment ELISA Kit; NTF); Intracellular domain 1 ELISA Kit; ICD1); Intracellular domain 2 ELISA Kit; ICD2); C-domain 1; C-domain 2; Tumor necrosis factor ELISA Kit; soluble form] ELISA Kit
Function
Cytokine that binds to TNFRSF1A/TNFR1 and TNFRSF1B/TNFBR. It is mainly secreted by macrophages and can induce cell death of certain tumor cell lines. It is potent pyrogen causing fever by direct action or by stimulation of interleukin-1 secretion and is implicated in the induction of cachexia, Under certain conditions it can stimulate cell proliferation and induce cell differentiation. Induces insulin resistance in adipocytes via inhibition of insulin-induced IRS1 tyrosine phosphorylation and insulin-induced glucose uptake. Induces GKAP42 protein degradation in adipocytes which is partially responsible for TNF-induced insulin resistance. Plays a role in angiogenesis by inducing VEGF production synergistically with IL1B and IL6.; The TNF intracellular domain (ICD) form induces IL12 production in dendritic cells.
Subcellular Location
Cell membrane; Single-pass type II membrane protein.; [Tumor necrosis factor, membrane form]: Membrane; Single-pass type II membrane protein.; [Tumor necrosis factor, soluble form]: Secreted.; [C-domain 1]: Secreted.; [C-domain 2]: Secreted.
Protein Families
Tumor necrosis factor family
Database Links
Precision

Intra-assay Precision (Precision within an assay): CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess.

Inter-assay Precision (Precision between assays): CV%<10%

Three samples of known concentration were tested in twenty assays to assess.

Typical Data

These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.

Rat TNF-α ELISA kit

pg/ml

OD1

OD2

Average

Corrected

1000

2.717

2.634

2.675

2.487

500

1.476

1.467

1.471

1.283

250

0.853

0.908

0.881

0.693

125

0.608

0.629

0.619

0.431

62.5

0.395

0.381

0.388

0.200

31.2

0.281

0.293

0.287

0.099

15.6

0.218

0.207

0.213

0.025

0

0.191

0.185

0.188

Linearity

To assess the linearity of the assay, samples were spiked with high concentrations of rat TNF-α in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.

Sample

cell culture supernates(n=4)

1:1

Average %

107

Range %

99-113

1:2

Average %

99

Range %

96-105

1:4

Average %

103

Range %

97-109

1:8

Average %

99

Range %

94-102

Recovery

The recovery of rat TNF-α spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.

Sample Type

Average % Recovery

Range

cell culture supernates (n=5)

94

89-100

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