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CUGBP1 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Marke: Proteintech 13002-1-AP-20UL
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Beschreibung
Myotonic dystrophy (MD) is an autosomal domit neuromuscular disease that is associated with a (CTG)n repeat expansion in the 3′-untranslated region of the myotonin protein kinase (Mt-PK) gene. A (CUG) n oligonucleotides triplet repeat pre-mRNA/mRNA binding protein may play an important role in DM pathogenesis. HeLa cell protein, CUG-BP1, has been purified based upon its ability to bind specifically to (CUG) 8 oligonucleotides in vitro. CUG-BP1 is the major (CUG) 8 binding activity in normal cells. CUG-BP1 has been identified as isoforms of a novel heterogeneous nuclear ribonucleoprotein (hnRNP), hNab50. The CUG-BP/hNab50 protein is localized predomitly in the nucleus and is associated with polyadenylated RNAs in vivo. In vitro RNA-binding/photocrosslinking studies demonstrate that CUG-BP/hNab50 binds to RNAs containing the Mt-PK 3-UTR. The (CUG) n repeat region in Mt-PK mRNA is a binding site for CUG-BP/hNab50 in vivo, and triplet repeat expansion leads to sequestration of this hnRNP on mutant Mt-PK transcripts.Spezifikation
CUGBP1 | |
Polyclonal | |
Unconjugated | |
CELF1 | |
Bruno like protein 2, BRUNOL2, CELF 1, CELF1, CUG BP, CUG BP1, CUGBP, CUGBP1, Deadenylation factor CUG BP, EDEN BP homolog, hNab50, NAB50, RNA binding protein BRUNOL 2 | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
10658, 13046, 362160 | |
-20°C | |
Liquid |
Immunofluorescence, Western Blot, Immunohistochemistry (Paraffin), Immunoprecipitation, Immunocytochemistry | |
0.37 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
P28659, Q4QQT3, Q92879 | |
Celf1 | |
CUGBP1 Fusion Protein Ag3677 | |
20 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |