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Anti -MAP Kinase Kinase 6, NT (Stress-activated Protein Kinase, SKK3, MKK6) Pricing   For pricing information, USA customers sign in.   Outside USA? Please contact your distributor for pricing. Specifications Clone Host Grade Applications Monoclonal Rabbit Supernatant B IP Mitogen-acitvated protein kinase kinase 6 (MKK6) belongs to the serine/threonine protein kinase family and the MAPK kinase subfamily (MAP2K, MKK or MEKs). MAPKs require dual phosphorylation on threonine and tyrosine residues, an activation step carried out by MAPK kinase (1-2). MKK6, closely related to MKK3, efficiently phosphorylates and activates p38 MAP kinase in response to inflammatory cytokines and environmental stress but not JNK or ERK (3). MTK1 phosphorylates MKK6 on serine 207 and threonine 211 (4). Catalog # M2363-22N Applications Suitable for use in Western Blot, Immunoprecipitation. Other applications not tested. Recommended Dilution Western Blot: 1:5,000-20,000 Immunoprecipitation: 1:50 Optimal dilutions to be determined by the researcher. Storage and Stability May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot Freeze at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. Clone Type Monoclonal Isotype IgG Clone No 6k263 Host Rabbit Source Human Form Supplied as a liquid. Purity Supernatant Immunogen A synthetic peptide corresponding to residues in the N-term of human MKK6 Specificity Recognizes human MKK6 Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.    Questions or comments about this product? Inquire here.    Download Specifications for Anti -MAP Kinase Kinase 6, NT (Stress-activated Protein Kinase, SKK3, MKK6) External Links Search PubMed. Search Google Scholar.