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Sunlong Medical™ Human Apolipoprotein H/Apo H ELISA Kit
Sunlong Medical™ Human Apolipoprotein H/Apo H ELISA Kit
APOH elisa kit | apolipoprotein H elisa kit | activated protein C-binding protein | anticardiolipin cofactor | APC inhibitor | apo-H | apolipoprotein H beta-2-glycoprotein I | B2G1 | B2GP1 | B2GPI | beta-2-glycoprotein 1 | beta2GPI | BG
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Details

Cat NO.:
EL0177Hu
Product:
Sunlong Medical™ Human Apolipoprotein H/Apo H 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:
88% - 116%
Mean Spike Recovery:
1.03
CV of Intra plate:
2.4% - 6.3%
CV of Inter plate:
3.9% - 4.6%
NCBI_Gene:
350
UniProtKB:
P02749

 

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-Apolipoprotein H/Apo H monoclonal antibody
Human Apolipoprotein H/Apo H freeze-dried standard
Apolipoprotein H/Apo H 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-human Apo H antibodies are precoated on a high-affinity ELISA plate. Standard samples and test samples are added to the wells of the ELISA plate for incubation. After washing to remove unbound substances, the detection antibody labeled with horseradish peroxidase is added for further incubation. 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 Apo H in the samples.A stop solution is added to terminate the reaction, and the absorbance value ismeasured at a wavelength of 450 nm (with a reference wavelength range of 570-630 nm).

 

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