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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 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
基因别名: 2410004J23Rik; 4933440I19Rik; SMNDC1; SMNR; SPF30; TDRD16C
UniProt ID: (Human) O75940, (Mouse) Q4QQL0
Entrez Gene ID: (Human) 10285, (Mouse) 76479