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Sunlong Medical™ Human alpha-Galactosidase A/GLA ELISA Kit
Sunlong Medical™ Human alpha-Galactosidase A/GLA ELISA Kit
GLA elisa kit | galactosidase alpha elisa kit | agalsidase alfa | alpha-D-galactosidase A | alpha-D-galactoside galactohydrolase 1 | alpha-gal A | alpha-galactosidase A | GALA | galactosidase | alpha | galactosylgalactosylglucosylceramidase GLA | melibias
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  • NO.:EL0125Hu
    Species:Human
    Assay range:0.5ng/mL-32ng/mL
    Sensitivity:53.55 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
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Details

Cat NO.:
EL0125Hu
Product:
Sunlong Medical™ Human alpha-Galactosidase A/GLA 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:
73% - 127%
Mean Spike Recovery:
0.93
CV of Intra plate:
4.9% - 8.8 %
CV of Inter plate:
3.6% - 8.0%
NCBI_Gene:
2717
UniProtKB:
P06280
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-alpha-Galactosidase A/GLA monoclonal antibody
Human alpha-Galactosidase A/GLA freeze-dried standard
Human alpha-Galactosidase A/GLA detect Antibody
Standard Diluent
Assay Buffer(10×)
Substrate TMB
Stop Solution
Washing Buffer(20×)
Sealing Film
ASSAY PRINCIPLE This kit utilizes a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) technique. Specific anti-human GLA antibodies are pre-coated on a high-affinity ELISA plate. Standard samples and test samples are added to the wells of the ELISA plate. After incubation, the GLA present in the sample binds to the solid-phase antibody. After washing to remove unbound substances, detection antibodies labeled with horseradish peroxidase (HRP) are added and incubated. After washing to remove unbound detection antibodies, the TMB chromogenic substrate is added for color development while avoiding light. The intensity of the color reaction is directly proportional to the concentration of GLA in the sample. The reaction is terminated by adding a stop solution, and the absorbance value is measured at a wavelength of 450 nm (with a reference wavelength range of 570-630 nm).

  

 

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