Imagine indisponibilăRat PERK ELISA Kit
Pe scurt
Rat PERK ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea PERK, cu reactivitate declarată pentru Rat. Măsoară în domeniul 46.875-3000 pg/ml, are o sensibilitate de 28.125 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 4.392,30 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rat PERK ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat PERK in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- PERK
- Applications
- Sandwich ELISA
- Reactivity
- Rat
- Recommended dilutions
- Validated sample dilutions include Rat liver tissue lysate (1:2) and Rat brain tissue lysate (1:2).
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 28.125 pg/ml
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 46.875-3000 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Rat PERK ELISA Kit (A87194) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat PERK in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for PERK. Standards and samples are added to the wells, where PERK binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for PERK is added to the wells. The detection antibody binds the captured PERK 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 PERK captured in each well. The concentration of PERK is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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