Imagine indisponibilăMouse VIP ELISA Kit
Pe scurt
Mouse VIP ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea VIP, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 12.5-800 pg/ml, are o sensibilitate de 7.5 pg/ml și folosește detecție Colorimetric Detection (OD450). Se livrează în mărimea 96T, la prețul de 3.746,77 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse VIP ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse VIP in serum, plasma, cell culture supernatant, cell or tissue lysate, and other liquid samples.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- VIP
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Recommended dilutions
- Validated sample dilutions include Healthy serum (undiluted) and Healthy plasma (undiluted).
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 7.5 pg/ml
- Sample type
- Serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 12.5-800 pg/ml
- Assay Time
- 2 hours
- Principiul testului
- Mouse VIP ELISA Kit (A336593) is a 2 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse VIP in serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids. This QuickRun format uses a pre-coated 96-well microtiter plate and optimized ready-to-use reagents to reduce assay time. Standards and samples are added to the wells, where VIP binds to the immobilized capture antibody. Assay-specific biotinylated detection antibody and HRP-Streptavidin reagents are then added according to the optimized QuickRun workflow. These reagents form an antibody-antigen-antibody sandwich complex with the captured VIP. TMB substrate solution is 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 VIP captured in each well. The concentration of VIP is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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