KD-Validated Poly(A) Binding Protein Nuclear 1 Recombinant Rabbit Monoclonal Antibody

KD-Validated Poly(A) Binding Protein Nuclear 1 Recombinant Rabbit Monoclonal Antibody

Cat. No.: KVAb00997
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Gene Name:PABPN1
Category: KO&KD Validated Antibodies Tags: , , , , , , , ,

Summary

Production Name

KD-Validated Poly(A) Binding Protein Nuclear 1 Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,ICC

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

PABPN1

Alternative Names

PABPN1; Poly(A) Binding Protein Nuclear 1; PAB2 ; PABP2; Polyadenylate-Binding Protein 2; PABP-2; PABII; OPMD; Polyadenylate-Binding Nuclear Protein 1; Poly(A)-Binding Protein, Nuclear 1; Poly(A) Binding Protein, Nuclear 1; Nuclear Poly(A)-Binding Protein 1; Poly(A) Binding Protein II; Poly(A)-Binding Protein II; Poly(A) Binding Protein 2; Poly(A)-Binding Protein 2

Gene ID

8106

SwissProt ID

Q86U42

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; FC 1:200-1:2,000; ICC 1:100-1:1,000

Molecular Weight

Calculated MW: 32.7kDa

 

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. [provided by RefSeq, Dec 2010]

 

Research Area

Epigenetics and Nuclear Signaling

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