Sunlong Medical™ Human TNF-α High Sensitivity ELISA Kit_High Sensitivity ELISA Kit_Sunlong Medical™

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Sunlong Medical™ Human TNF-α High Sensitivity ELISA Kit

Total

Product Summary

NO.:HS-EL0048Hu

Species:Human

Assay range:1.56pg/mL-100pg/mL

Sensitivity:0.16 pg/mL

Sample Volume:Serum | plasma;20 μL；Cell culture supernatant;100 μL

Assay type:Sandwich Method

Validity:Two Years

Manual

Product Spec:

48T

96T

Number:

Details

Cat NO.:	HS-EL0048Hu
Product:	Sunlong Medical™ Human TNF-α High Sensitivity ELISA Kit
Storage	4℃ (unopened) for two years
Shipping Condition	4℃
Sample Type:	Serum \| plasma \| cell culture supernatant and other biological samples
Spike Recovery Range:	100% - 108%
Mean Spike Recovery:	1.04
CV of Intra plate:	4.1 % - 4.8 %
CV of Inter plate:	5.4% - 7.0%
NCBI_Gene:	7124
UniProtKB:	P01375

PLATFORM	ELISA
PLATE	Detachable 96-well plate
SIZE	96T/48T
STORAGE	If the reagent kit is unopened, it should be stored at 4℃. However, if it has been opened, the standard solution should be stored at -20℃, while the other components should be stored at 4℃.
DELIVERY	4℃ blue ice transportation
COMPONENTS	96-well polystyrene enzyme-linked immunosorbent assay (ELISA) plate coated with anti-TNF-α monoclonal antibody Human TNF-α freeze-dried standard TNF-α detect Antibody Standard Diluent HRP-labeled streptavidin Signal enhancer concentrate Signal enhancer diluent Assay Buffer(10×) Substrate TMB Stop Solution Washing Buffer(20×)
ASSAY PRINCIPLE	This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-human TNF-α antibodies are precoated on a high-affinity ELISA plate.Standards and test samples are added to the wells of the ELISA plate. After incubation, the TNF-α present in the samples binds to the solid-phase antibodies. After washing to remove unbound substances, biotinylated detection antibodies are added and incubated. After washing to remove unbound biotinylated antibodies, streptavidin-HRP labeled with horseradish peroxidase is added. After washing again, a signal enhancer is added and incubated. After washing to remove unbound substances, Streptavidin-HRP is added once more. After washing, a colorimetric substrate, TMB, is added and the plate is incubated in the dark for color development. The intensity of the color reaction is directly proportional to the concentration of TNF-α in the samples.A stop solution is added to terminate the reaction, and the absorbance value is measured at a wavelength of 450 nm (with a reference wavelength range of 570-630 nm).

Citations

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2.TIPE2 regulates periodontal inflammation by inhibiting NF-κB p65 phosphorylation

3.Fe-curcumin nanozyme-mediated immunosuppression and anti-inflammation in experimental autoimmune uveitis

4.Hypoxia-associated circPRDM4 promotes immune escape via HIF-1α regulation of PD-L1 in hepatocellular carcinoma

5.Kaempferol Reverses Acute Kidney Injury in Septic Model by Inhibiting NF-κB/AKT Signaling Pathway

6.Protective effect of small extracellular vesicles (EVs) derived from ACE2-modified human umbilical cord mesenchymal stem cells against renal ischemia–reperfusion injury

7.Maslinic acid attenuates UVB-induced oxidative damage in HFF-1 cells

Partial purchase records (19)

Username	Quantity	bought time
Wi***	3	2024-08-20
Ja***	1	2024-07-29
Be***	1	2024-07-23
We***	3	2024-07-22
Ja***	3	2024-07-09