anti-SNRPN Upstream Reading Frame (SNURF) Anticorps

SNURF encodes a highly basic protein localized to the nucleus. De plus, nous expédions SNRPN Upstream Reading Frame Protéines (8) et SNRPN Upstream Reading Frame Kits (4) et beaucoup plus de produits pour cette protéine.

afficher tous les anticorps Gène GeneID UniProt
SNURF 8926 Q9Y675
Anti-Souris SNURF SNURF 84704 Q9WU12
Anti-Rat SNURF SNURF 113938 Q9WU11
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Top anti-SNRPN Upstream Reading Frame Anticorps sur anticorps-enligne.fr

Showing 5 out of 6 products:

Catalogue No. Reactivité Hôte Conjugué Application Images Quantité Livraison Prix Détails
Humain Lapin Inconjugué EIA, WB 0.4 mL 6 to 8 Days
$484.00
Détails
Humain Souris Inconjugué IF, WB Western Blot analysis of SNURF expression in transfected 293T cell line by SNURF MaxPab polyclonal antibody.Lane 1: SNURF transfected lysate(26.51 KDa).Lane 2: Non-transfected lysate. Immunofluorescence of purified MaxPab antibody to SNURF on HeLa cell. [antibody concentration 10 ug/ml] 50 μL 11 to 12 Days
$440.00
Détails
Humain Lapin Inconjugué ELISA, WB   200 μL 11 to 16 Days
$658.43
Détails
Humain Lapin Inconjugué FACS, IHC, IHC (p), WB   400 μL 11 to 14 Days
$493.17
Détails
Humain Souris Inconjugué IF, WB   50 μg 11 to 16 Days
$625.43
Détails

Plus d’anticorps contre SNRPN Upstream Reading Frame partenaires d’interaction

Human SNRPN Upstream Reading Frame (SNURF) interaction partners

  1. A de novo 6.4 kb deletion at 15q11.2, containing exon 1 of the SNURF gene and exon 1 of the shortest isoform of the SNRPN gene was identified in a patient with Prader-Willi-like phenotype. DNA methylation analysis confirmed the paternal origin of the deletion.

  2. significant IGF2 hypermethylation (20 +/- 10 vs. 14 +/- 7%; p<0.05) and SNURF hypomethylation (23 +/- 6 vs. 32 6%; p<0.001) was found in Albright's hereditary osteodystrophy patients vs. controls.

  3. Differences between genetic subtypes were also statistically significant in Prader Willi syndrome

  4. The SNURF-SNRPN sense/UBE3A antisense transcription unit spans more than 460 kb.

  5. Identification of cis- and trans-acting regulatory elements within the endogenous SNURF-SNRPN locus.

Mouse (Murine) SNRPN Upstream Reading Frame (SNURF) interaction partners

  1. the ATG-to-AAG 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

SNRPN Upstream Reading Frame (SNURF) profil antigène

Profil protéine

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.

Gene names and symbols associated with SNURF

  • SNRPN upstream reading frame (SNURF) anticorps
  • small nuclear ribonucleoprotein polypeptide N (SNRPN) anticorps
  • SNRPN upstream reading frame (Snurf) anticorps
  • 2410045I01Rik anticorps
  • Snrpn anticorps

Protein level used designations for SNURF

SNRPN upstream reading frame , SNRPN upstream reading frame protein , small nuclear ribonucleoprotein N

GENE ID SPECIES
606883 Canis lupus familiaris
744238 Pan troglodytes
8926 Homo sapiens
84704 Mus musculus
113938 Rattus norvegicus
282076 Bos taurus
100009465 Oryctolagus cuniculus
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