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>   home   >   Products   >   Primary Antibodies   >   Cell Biology   >   SNURF Antibody (Center)   

SNURF Antibody (Center)

Purified Rabbit Polyclonal Antibody (Pab)

Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q9Y675
Other Accession Q9XS97, Q9WU12, Q9XS96
Reactivity Human
Predicted Mouse, Rabbit, Bovine
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 8412 Da
Antigen Region 4-32 aa
Additional Information
Gene ID 8926
Other Names SNRPN upstream reading frame protein, SNURF
Target/Specificity This SNURF antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 4-32 amino acids from the Central region of human SNURF.
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsSNURF Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Cellular Location Nucleus.
Tissue Location Expressed in heart, skeletal muscle and lymphoblasts (at protein level). Expressed in brain, pancreas, heart, liver, lung, kidney and skeletal muscle
Research Areas
Citations (0)

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SNURF is a highly basic protein localized to the nucleus. The evolutionarily constrained open reading frame of its gene 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.


Rodriguez-Jato,S., Nucleic Acids Res. 33 (15), 4740-4753 (2005)
Runte,M., Hum. Genet. 114 (6), 553-561 (2004)
Runte,M., Hum. Mol. Genet. 10 (23), 2687-2700 (2001)

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$ 295.00
$ 99.00
Cat# AP2816c
(40 western blots)
Availability: In Stock
Bulk Size
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