SMNDC1 Antibody - C-terminal region : Biotin (ARP40611_P050-Biotin)

This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. SMNDC1 is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.

UBC; PRPF3; SF3B5; SND1; CUL3; SF3A2; ELAVL1; HIST3H3; mad2; KPNB1; SNRNP200; SNRPB; CDK5RAP3; PPAN; TSR1; RNMTL1; SF3B1; SF3B3; SF3B2; SF3A3; SF3B4; DDX21; RUVBL1; RPL3; FDFT1; EWSR1

All conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil) . Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -20C to -80C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.