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SNURF encodes a highly basic protein localized to the nucleus. Additionally we are shipping SNRPN Upstream Reading Frame Proteins (7) and SNRPN Upstream Reading Frame Kits (4) and many more products for this protein.
Showing 8 out of 9 products:
Human Polyclonal SNURF Primary Antibody for FACS, IHC (p) - ABIN389318
Rodriguez-Jato, Nicholls, Driscoll, Yang: Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus. in Nucleic acids research 2005
Show all 3 references for ABIN389318
Human Polyclonal SNURF Primary Antibody for EIA, WB - ABIN357983
Runte, Kroisel, Gillessen-Kaesbach, Varon, Horn, Cohen, Wagstaff, Horsthemke, Buiting: SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. in Human genetics 2004
Show all 3 references for ABIN357983
significant IGF2 hypermethylation (20 +/- 10 vs. 14 +/- 7%; p<0.05) and SNURF (show RNF4 Antibodies) hypomethylation (23 +/- 6 vs. 32 6%; p<0.001) was found in Albright's hereditary osteodystrophy patients vs. controls.
The SNURF-SNRPN sense/UBE3A (show ube3a Antibodies) antisense transcription unit spans more than 460 kb.
Identification of cis (show CISH Antibodies)- and trans-acting regulatory elements within the endogenous SNURF-SNRPN locus.
the ATG-to-AAG (show C16orf35 Antibodies) mutation causes a 15-fold or more increase in translation of the downstream ORF in two fusion constructs, and it is likely that similar translational control affects the normal Snurf-Snrpn transcript as well
This gene encodes a highly basic protein localized to the nucleus. The evolutionarily constrained open reading frame is found on a bicistronic transcript which has a downstream ORF encoding the small nuclear ribonucleoprotein polypeptide N. The upstream coding region utilizes the first three exons of the transcript, a region that has been identified as an imprinting center. Multiple transcription initiation sites have been identified and extensive alternative splicing occurs in the 5' untranslated region but the full-length nature of these transcripts has not been determined. An alternate exon has been identified that substitutes for exon 4 and leads to a truncated, monocistronic transcript. Alternative splicing or deletion caused by a translocation event in the 5' UTR or coding region of this gene leads to Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure. The function of this protein is not yet known.
SNRPN upstream reading frame
, SNRPN upstream reading frame protein
, small nuclear ribonucleoprotein N