SNURF antibody, Internal

GeneTex

SNURF antibody, Internal

9

ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin

Research Use Only

Polyclonal

Unconjugated

SNRPN

small nuclear ribonucleoprotein polypeptide N

HCERN3; PWCR; RT-LI; sm protein D; SM protein N; small nuclear ribonucleoprotein-associated protein N; SM-D; SMN; sm-N; SNRNP-N; SNURF-SNRPN; tissue-specific splicing protein

Rabbit

IgG

Small nuclear ribonucleoprotein-associated protein N

This gene is located within the Prader-Willi Syndrome critical region on chromosome 15. Transcripts produced from this gene initiate at an imprinting center and are paternally-imprinted. These transcripts may be bicistronic and also encode SNRPN (small nuclear ribonucleoprotein polypeptide N) from a downstream open reading frame. The small protein represented by this gene is encoded by an evolutionarily-conserved upstream open reading frame and is localized to the nucleus. Extensive alternative splicing and promoter usage occurs in this region and the full-length nature of some of these transcripts has not been determined. Alterations in the imprinting center are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]

Human

-20°C or -80°C,2°C to 8°C

12352203