rna-isolation-purification-cells-primary-mouse-dorsal-root-ganglion-neurons

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Get tips on using FuGENE® 6 Transfection Reagent to perform DNA transfection Mammalian cells - Primary cells Human chondrocytes

Products Promega FuGENE® 6 Transfection Reagent

Get tips on using Lipofectamine™ 3000 Transfection Reagent to perform DNA transfection Mammalian cells - Primary cells Human chondrocytes

Products Thermo Fisher Scientific Lipofectamine™ 3000 Transfection Reagent

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Mouse - NSC-34

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Mouse - BV-2

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using MagNA Pure Compact Nucleic Acid Isolation Kit I to perform DNA isolation / purification Bacteria - Gram negative Salmonella enterica

Products Roche Lifesciences MagNA Pure Compact Nucleic Acid Isolation Kit I

Get tips on using MagNA Pure Compact Nucleic Acid Isolation Kit I to perform DNA isolation / purification Bacteria - Gram negative Helicobacter pylori

Products Roche Lifesciences MagNA Pure Compact Nucleic Acid Isolation Kit I

Get tips on using MagNA Pure Compact Nucleic Acid Isolation Kit I to perform DNA isolation / purification Bacteria - Gram negative Pseudomonas aeruginosa

Products Roche Lifesciences MagNA Pure Compact Nucleic Acid Isolation Kit I

Get tips on using PowerSoil® DNA isolation - DNeasy PowerSoil Pro Kit to perform DNA isolation / purification Bacteria - Gram positive Mycobacterium tuberculosis

Products Qiagen PowerSoil® DNA isolation - DNeasy PowerSoil Pro Kit

Get tips on using PowerSoil® DNA isolation - DNeasy PowerSoil Pro Kit to perform DNA isolation / purification Bacteria - Gram positive Lactobacillus amylovorus

Products Qiagen PowerSoil® DNA isolation - DNeasy PowerSoil Pro 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 Mouse BMP-2

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