SMNDC1 antibody (clone 2B9), anti-human

Background:
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.

Other Names:
Survival of motor neuron-related-splicing factor 30, 30 kDa splicing factor SMNrp, SMN-related protein, Survival motor neuron domain-containing protein 1, SMNDC1, SMNR, SPF30

Antigen Type:
Recombinant Protein

Gene Name: SMNDC1
Gene ID: 10285
NCBI Accession: NP_005862.1
Primary Accession: O75940
Other Accession: BC011234
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .