Imagine indisponibilăMouse PERK ELISA Kit
Pe scurt
Mouse PERK ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea PERK, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 78-5000 pg/ml, are o sensibilitate de 46.9 pg/ml și folosește detecție Colorimetric Detection (OD450). Se livrează în mărimea 96T, la prețul de 3.993,00 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse PERK ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse PERK in serum, plasma, cell culture supernatant, cell or tissue lysate, and other liquid samples.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- PERK
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 46.9 pg/ml
- Sample type
- Serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 78-5000 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Mouse PERK ELISA Kit (A326541) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse PERK in serum, plasma, cell culture supernatant, cell or tissue lysate, 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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