Cdk1/2/3(Phospho Thr14) Polyclonal Antibody, 50ul Buffers & Solutions Specific mutations in DYSF have

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

and may be involved in the nuclear and/or nucleolar targeting of the protein

10 µm Pore Size and PVDF Membrane

Ideal tool to avoid lab air contamination and protect personnel safety

Cdk1/2/3(Phospho Thr14) Polyclonal Antibody, 50ul Buffers & Solutions Specific mutations in DYSF haveThe protein encoded by this gene is a member of the Ser Thr protein kinase family. This protein is a catalytic subunit of the highly conserved protein kinase complex known as M phase promoting factor (MPF), which is essential for G1 S and G2 M phase transitions of eukaryotic cell cycle. Mitotic cyclins stably associate with this protein and function as regulatory subunits. The kinase activity of this protein is controlled by cyclin accumulation and