SMNDC1 cDNA
€0.00
In stock
SKU
ATGD0191
Description
SMNDC1 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.Alternative Names
SMNR, SPF30, TDRD16CConcentration
LyophilizedStorage: Store the plasmid at -20C.
SMNDC1 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.Alternative Names
SMNR, SPF30, TDRD16CConcentration
LyophilizedStorage: Store the plasmid at -20C.
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