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>   Home   >   Products   >   Primary Antibodies   >   PABPN1 Rabbit mAb   

PABPN1 Rabbit mAb

 
Catalog #
ABZ5103
Application
WB, IF, FC, IP, ICC, IHC-P
Uniprot Id
Q86U42
Reactivity
Human, Mouse, Rat
Isotype
IgG
 
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  • Western blot analysis of PABPN1 in HeLa lysates using PABPN1 antibody.
 Catalog #AvailabilitySizeQuantityUnit Price Save For Later Wish List
ABZ5103-100 2 weeks 100 µL $499.00
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ABZ5103-20 2 weeks 20 µL $149.00
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Product Overview

NamePABPN1 Rabbit mAb
Accession (Primary)Q86U42
Host SpeciesRabbit
ClonalityMonoclonal
IsotypeIgG
Species Reactivity
Reacts WithHuman, Mouse, Rat
Calculated MW
Calculated MW: 33 kDa; Observed MW: 49 kDa
Buffer System
Liquid in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
Storage
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Recommended Dilution
WB-1:1000-1:5000; IHC-P-1:200-1:1000; ICC/IF-1:100-1:200; FC-1:20-1:50; IP-1:20-1:50
Purification
Affinity Chromatography
Conjugation
Unconjugated
Modification
Unmodified
Form
Liquid
Background
This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein is required for progressive and efficient polymerization of poly(A) tails at the 3' ends of eukaryotic transcripts and controls the size of the poly(A) tail to about 250 nt. At steady-state, this protein is localized in the nucleus whereas a different poly(A) binding protein is localized in the cytoplasm. This gene contains a GCG trinucleotide repeat at the 5' end of the coding region, and expansion of this repeat from the normal 6 copies to 8-13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease. Related pseudogenes have been identified on chromosomes 19 and X. Read-through transcription also exists between this gene and the neighboring upstream BCL2-like 2 (BCL2L2) gene.

Target Information: ( Q86U42 )

NamePABPN1
Gene ID8106
Other Names
OPMD; PAB2; PABII; PABP2; PABP-2
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