Imagine indisponibilăCEBPD + E Cell Based ELISA Kit
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CEBPD + E Cell Based ELISA Kit este un kit ELISA de tip Cell-based (qualitative) pentru măsurarea CEBP delta + CEBPE, cu reactivitate declarată pentru Human, Mouse, Rat. Măsoară în domeniul > 5000 Cells, folosește detecție Colorimetric și se poate folosi pe probe de tip Adherent and suspension cells. Se livrează în mărimea 96T, la prețul de 3.826,63 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
CEBPD + E Cell Based ELISA Kit is a Enzyme-Linked Immunosorbent Assay designed for the indirect in vitro quantitative determination of CEBP delta + CEBPE levels in adherent and suspension cells.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- CEBP delta + CEBPE
- Applications
- Cell-Based ELISA
- Reactivity
- Human, Mouse, Rat
- Assay type
- Cell-based (qualitative)
- Sample type
- Adherent and suspension cells.
- Cross reactivity
- No reported cross-reactivity.
- Detection type
- Colorimetric
- Product range
- > 5000 Cells
- Assay Time
- 4 hours 30 minutes
- Principiul testului
- This CEBPD + E Cell-Based ELISA Kit allows for the detection of CEBPD + E and the effects that certain stimulation conditions have on CEBPD + E expression in different cell lines. Qualitative determination of CEBPD + E concentration is achieved by an indirect ELISA format. In essence, the CEBPD + E is captured by Anti-CEBPD + E Antibodies which in turn are detected by HRP-conjugated secondary antibodies. Through this binding, the HRP enzyme (conjugated to the secondary antibody) can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of this CEBPD + E Cell-Based ELISA Kit, multiple normalization methods are described: 1) Anti-GAPDH Antibody is included to serve as an internal positive control in normalizing the target absorbance values. 2) Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method is used to determine cell density. After staining, the results can be analyzed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted.
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