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Recommended positive controls: NT2D1, IMR32, U87-MG, MCF-7.
Predicted reactivity: Mouse (99%), Rat (99%), Pig (98%), Rhesus Monkey (99%), Bovine (98%).
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: 30 kDa splicing factor SMNrp; MGC106917; MGC112663; SMN related protein; SMN-related protein; splicing factor 30, survival of motor neuron-related; Survival motor neuron domain-containing protein 1; Survival of motor neuron-related-splicing factor 30; tudor domain containing 16C
Gene Aliases: 2410004J23Rik; 4933440I19Rik; SMNDC1; SMNR; SPF30; TDRD16C
UniProt ID: (Human) O75940, (Mouse) Q8BGT7
Entrez Gene ID: (Human) 10285, (Mouse) 76479
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