Immunohistochemistry chk2 Rabbit IgG Human

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Get tips on using RediPlate™ 96 RiboGreen™ RNA Quantitation Kit to perform RNA quantification Fuorimetric - human brain tissue

Products Thermo Fisher Scientific RediPlate™ 96 RiboGreen™ RNA Quantitation Kit

Get tips on using Quant-iT™ RiboGreen™ RNA Assay Kit to perform RNA quantification Fuorimetric - human trophoblast cells

Products Thermo Fisher Scientific Quant-iT™ RiboGreen™ RNA Assay Kit

Get tips on using EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit to perform ChIP Human - Glioblastoma cell line

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Get tips on using SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003 to perform ChIP Human - Glioblastoma cell line

Products Cell Signaling Technology SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003

Get tips on using EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit to perform ChIP Human - Fibroblast cell lines

Products Merck Millipore EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit

Get tips on using GeneArt™ CRISPR Nuclease Vector with OFP Reporter Kit to perform CRISPR Human - Deletion DJ-1

Products Thermo Fisher Scientific GeneArt™ CRISPR Nuclease Vector with OFP Reporter Kit

Get tips on using SimpleChIP® Plus Enzymatic Chromatin IP Kit (Agarose Beads) #9004 to perform ChIP Human - PANC-1

Products Cell Signaling Technology SimpleChIP® Plus Enzymatic Chromatin IP Kit (Agarose Beads) #9004

Get tips on using Corning® BioCoat™ Angiogenesis System: Endothelial Cell Tube Formation to perform Angiogenesis assay human - HMVEC

Products Corning Corning® BioCoat™ Angiogenesis System: Endothelial Cell Tube Formation

Get tips on using Cultrex® In Vitro Angiogenesis Assay Endothelial Cell Invasion Kit to perform Angiogenesis assay human - HMVEC

Products Trevigen Cultrex® In Vitro Angiogenesis Assay Endothelial Cell Invasion Kit

ELISA is the most commonly used method of detecting and quantifying the concentration of an antigen in an unknown sample. During the experiment, If you get a weak signal, then make sure reagents are at room temperature before starting the assay. Try increasing incubation times to ensure maximal antibody binding and amplify the signal. Secondly, if you get values above 0 in the negative control indicates a high background signal. Try to consider reducing your antibody concentration and prevent non-specific binding of antibodies by using affinity-purified antibody and suitable blocking buffers. To avoid high well to well variation, do not stack plates during incubation, no bubbles in the plate and wash wells thoroughly to avoid variation.

Proteins ELISA Rat IGF-I

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