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.

Codice: E-AB-18953_120μL | Marca: Elabscience | Confezionamento: 120μL

Specie: Human;Mouse;RatIsotipo: IgGConiugazione: Unconjugated

Torna alla lista Apri link

Codice: E-AB-18953_120μL
Marca: Elabscience
Specie target: Human;Mouse;Rat
Host: Rabbit
Concentrazione: 0.6 mg/mL
Link: Apri link
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: IHC
Diluizione: IHC 1:40-1:200
Simbolo target: SMNDC1
Ig target: 30 kDa splicing factor SMNrp;MGC106917;MGC112663;SMN related protein;SMN-related protein;smndc1;SMNR;SPF30;SPF30;Splicing factor 30; survival of motor neuron-related ;Survival motor neuron domain containing 1;Survival motor neuron domain containing protein 1;Survival motor neuron domain-containing protein 1;Survival of motor neuron related splicing factor 30;Survival of motor neuron-related-splicing factor 30
Area di ricerca: Cancer;Epigenetics and Nuclear Signaling;Metabolism

Scheda prodotto