Imagine indisponibilăRat LDLR ELISA Kit
Pe scurt
Rat LDLR ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea LDLR, cu reactivitate declarată pentru Rat. Măsoară în domeniul 0.313-20 ng/ml, are o sensibilitate de 0.188 ng/ml și folosește detecție Colorimetric Detection (OD450). Se livrează în mărimea 96T, la prețul de 4.186,00 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rat LDLR ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat LDLR in serum, plasma, cell culture supernatant, cell or tissue lysate, and other liquid samples.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- LDLR
- Applications
- Sandwich ELISA
- Reactivity
- Rat
- Recommended dilutions
- Validated sample dilutions include Healthy serum (1:5) and Healthy plasma (1:5).
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.188 ng/ml
- Sample type
- Serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.313-20 ng/ml
- Assay Time
- 2 hours
- Principiul testului
- Rat LDLR ELISA Kit (A336832) is a 2 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat LDLR 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 LDLR 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 LDLR. 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 LDLR captured in each well. The concentration of LDLR is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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