GTX82489
SNURF antibody, Internal
Cannot supply to this region.
- SKU:
- GTX82489
- Additional Names:
- SNRPN upstream reading frame
- Application:
- IHC-P
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- SAS Precipitated; Dialysis
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 0.09% Sodium azide.
- Immunogen:
- KLH conjugated synthetic peptide between 4-32 amino acids from the Central region of human SNURF.
- Uniprot:
- P63162, Q9Y675
- Synonyms:
- HCERN3;PWCR;RT-LI;sm protein D;SM protein N;SM-D;sm-N;small nuclear ribonucleoprotein-associated protein N;SMN;SNRNP-N;SNRPN upstream reading frame protein;SNURF-SNRPN;tissue-specific splicing protein;Tissue-specific-splicing protein
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice