Phospho-ERK1/2 (Thr202/Tyr204) Translocation Assay Kit (Cell-Based)

Alternate Name :

Tag Line :

A cell-based assay kit that detect the nuclear translocation of activated ERK1/2 in fixed mammalian cells.

Storage Conditions: -20°C

Shelf life: 12 months

Summary :

• Detection method- fluorescence microscope capable of measuring EX at 570 nm and equipped with UV filter for DAPI
• Species reactivity- Human, mouse, rat
• Application- Detection of nuclear translocation of phosphorylated-ERK1/2 in mammalian cells

Detection Method: fluorescence microscope capable of measuring EX at 570 nm and equipped with UV filter for DAPI

Features & Benefits:

• Detection of subcellular localization of activated ERK1/2 in mammalian cells
• Screening and characterizing effectors of ERK1/2 kinases
• Studying of cell signaling, cell division and cell proliferation mechanism

Description:

Mitogen-activated protein kinases (MAPKs) are proline-directed serine and threonine protein kinases that regulate numerous physiological cell responses including: embryogenesis, cell differentiation, proliferation, migration, apoptosis and death. Extracellular signal-regulated kinases (ERKs) 1 and 2 (ERK1/2), also known as p44 MAPK and p42 MAPK respectively, belong to one of the five major groups of MAPKs. Closely-related ERK1/2 isoforms are uniquely activated by several extracellular signals including growth factors, cytokines, hormones, and neuro-transmitters. Activation of ERK1/2 by the upstream kinases MEK1 and MEK2 occurs via dual phosphorylation on specific threonine (Thr202) and tyrosine (Tyr204) residues on the T*EY* motif. MEK1 and MEK2 are activated through receptors (tyrosine kinases or integrins) via pathways involving adaptor proteins, guanine nucleotide exchange factors, small GTP binding proteins, and MAPKKs. Activated ERK1/2 phosphorylates both, cytosolic (SOS, MNK1/2, RSKs) and nuclear targets. In the nucleus, it affects gene expression and DNA replication by the phosphorylation of MSK 1 and 2 and the transcription factors Elk-1, Sap1, and Sap2. In cultured cells, growth factors or mitogens induce rapid and transient translocation of activated ERK1/2 to nucleus. Different cell lines exhibit various duration, magnitude, and subcellular localization of activated/phosphorylated ERK1/2. The response of the protein may differ even within the same cell line depending on the dose and cell density. BioVision’s Phospho-ERK1/2 (Thr202/Tyr204) Translocation Assay Kit provides a simple and complete assay in a ready-to-use format to visualize the translocation of activated ERK1/2 between cytoplasmic and nuclear compartments in mammalian cells.