Imagine indisponibilăMouse GAPDH ELISA Kit
Pe scurt
Mouse GAPDH ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea GAPDH, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 0.313-20 ng/ml, are o sensibilitate de 0.188 ng/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
Mouse GAPDH ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse GAPDH in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- GAPDH
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Recommended dilutions
- Validated sample dilutions include 4T1 cell lysate (1:1000-1:2000) and Raw264.7 cell lysate (1:1000-1:2000).
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.188 ng/ml
- Cross reactivity
- Specific for GAPDH with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.313-20 ng/ml
- Assay Time
- 4 hours
- Principiul testului
- Mouse GAPDH ELISA Kit (A76595) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse GAPDH in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for GAPDH. Standards and samples are added to the wells, where GAPDH binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for GAPDH is added to the wells. The detection antibody binds the captured GAPDH 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 GAPDH captured in each well. The concentration of GAPDH is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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