Imagine indisponibilăHuman DAK/Triokinase/FMN Cyclase ELISA Kit
Pe scurt
Human DAK/Triokinase/FMN Cyclase ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea DAK/Triokinase/FMN Cyclase, cu reactivitate declarată pentru Human. Măsoară în domeniul 15.625-1000 pg/ml, are o sensibilitate de 9.375 pg/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum, plasma, tissue homogenates, and other biological fluids. Se livrează în mărimea 96T, la prețul de 4.591,95 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human DAK/Triokinase/FMN Cyclase ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human DAK/Triokinase/FMN Cyclase in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 9.375 pg/ml
- Cross reactivity
- Specific for DAK/Triokinase/FMN Cyclase with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 15.625-1000 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Human DAK/Triokinase/FMN Cyclase ELISA Kit (A303228) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human DAK/Triokinase/FMN Cyclase in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for DAK/Triokinase/FMN Cyclase. Standards and samples are added to the wells, where DAK/Triokinase/FMN Cyclase binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for DAK/Triokinase/FMN Cyclase is added to the wells. The detection antibody binds the captured DAK/Triokinase/FMN Cyclase to form an antibody-antigen-antibody sandwich complex. After further incubation and washing, HRP-Streptavidin conjugate is added to the wells. TMB substrate solution is then added to visualize the HRP enzymatic reaction. This produces a blue-coloured product that changes to yellow following addition of acidic stop solution. The intensity of the yellow colour is directly proportional to the amount of DAK/Triokinase/FMN Cyclase captured in each well. The concentration of DAK/Triokinase/FMN Cyclase is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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