M18BP Rabbit Polyclonal Antibody, 20ul RNA Tools 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

Its role in tissue remodeling and tumor invasion may be modulated by CSPG4

Multiple alleles of this gene exhibiting variations in the length of the tandem repeats| polymorphic cleavage sites and polymorphic stop codons have been identified

Interacts specifically with a number of opioid ligands

The first intron of CSF1R contains a transcriptionally inactive ribosomal protein L7 processed pseudogene oriented in the opposite direction

M18BP Rabbit Polyclonal Antibody, 20ul RNA Tools Specific mutations in DYSF have