Imagine indisponibilăMEF2A ELISA Kit
Pe scurt
MEF2A ELISA Kit este un kit ELISA de tip Indirect pentru măsurarea MEF2A, cu reactivitate declarată pentru Human, Mouse, Rat. Folosește detecție Colorimetric și se poate folosi pe probe de tip Nuclear lysates. Se livrează în mărimea 96T, la prețul de 4.625,23 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
MEF2A ELISA Kit is a Indirect Enzyme-Linked Immunosorbent Assay designed for the indirect in vitro quantitative determination of MEF2A levels in nuclear lysates.
Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- MEF2A
- Applications
- DNA-Binding ELISA
- Reactivity
- Human, Mouse, Rat
- Assay type
- Indirect
- Sample type
- Nuclear lysates.
- Cross reactivity
- No reported cross-reactivity.
- Detection type
- Colorimetric
- Principiul testului
- This MEF2A ELISA Kit applies the qualitative technique of an indirect ELISA. Streptavidin is bound to the immunoassay plate and specific biotinylated double stranded (dsDNA) oligonucleotides are then added to bind to the streptavidin via a high affinity biotin-streptavidin interaction. After subsequent blocking of extraneous binding sites in each well, the sample containing the target of interest can be added. Primary antibody is added to bind activated transcription factors bound to the dsDNA oligonucleotide, which has been immobilized via the plate-coated streptavidin. A HRP-conjugated secondary antibody specific for rabbit IgGs is added, which allows for specific binding to the Primary Antibody, and consequently colorimetric detection upon addition of the TMB substrate. For color development, TMB (3, 3’, 5, 5’-Tetramethylbenzidine) is added to each well. After addition of the substrate, a peroxidase catalyzed reaction will produce a blue TMB Diimine product that is proportional to the target concentration in the sample. Color development is quenched by addition of Stop Solution, or 2 N Sulfuric Acid, which turns the solution yellow. The absorbance can then be read by a spectrophotometer at 450 nm and subsequently allowing for determination of the target concentration in the sample.
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