Home > Sunlong Medical™ > High Sensitivity ELISA Kit > Sunlong Medical™ Rat IL-4 High Sensitivity ELISA Kit

Sunlong Medical™ Rat IL-4 High Sensitivity ELISA Kit

Sunlong Medical™ Rat IL-4 High Sensitivity ELISA Kit
Total

Product Summary

Alias:IL4 elisa kit | interleukin 4 elisa kit | B-cell growth factor 1 | B-cell IGG differentiation factor | B-cell stimulatory factor 1 | BSF-1 | IL-4 | Il4e12 | interleukin-4 | lymphocyte stimulatory factor 1

NO.:HS-EL0035Ra

Species:Rat

Assay range:3.13pg/mL-200pg/mL

Sensitivity:0.20 pg/mL

Sample Volume:20 μL

Assay type:Sandwich Method

Validity:Two Years

    Number:

Details

Cat NO.:
HS-EL0035Ra
Product:
Sunlong Medical™ Rat IL-4 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:
81% - 101%
Mean Spike Recovery:
90%
CV of Intra plate:
5.0 % - 6.8 %
CV of Inter plate:
2.7% - 7.5 %
NCBI_Gene:
287287
UniProtKB:
A0A0G2JVY1

 

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-IL-4 monoclonal antibody
Rat IL-4 freeze-dried standard
IL-4 detect Antibody
Standard Diluent
Assay Buffer(10×)
Substrate TMB
Stop Solution
Washing Buffer(20×)
Sealing Film
ASSAY PRINCIPLE This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-rat IL-4 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 IL-4 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 IL-4 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).

 

Partial purchase records (23)

UsernameQuantitybought time
He***22024-09-11
Um***22024-09-10
Um***12024-09-04
Di***12024-08-30
Sa***32024-08-20
Total 23 records, divided into5 pages. First Prev Next Last

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