Imagine indisponibilăHuman SH3GL1/EEN ELISA Kit
Pe scurt
Human SH3GL1/EEN ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea SH3GL1/EEN, cu reactivitate declarată pentru Human. Măsoară în domeniul 0.781-50 ng/ml, are o sensibilitate de 0.469 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
Human SH3GL1/EEN ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human SH3GL1/EEN in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- SH3GL1/EEN
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.469 ng/ml
- Cross reactivity
- Specific for SH3GL1/EEN with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.781-50 ng/ml
- Assay Time
- 4 hours
- Principiul testului
- Human SH3GL1/EEN ELISA Kit (A75833) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human SH3GL1/EEN in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for SH3GL1/EEN. Standards and samples are added to the wells, where SH3GL1/EEN binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for SH3GL1/EEN is added to the wells. The detection antibody binds the captured SH3GL1/EEN 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 SH3GL1/EEN captured in each well. The concentration of SH3GL1/EEN is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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