PABPN1 Polyclonal Antibody
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In stock
SKU
E-AB-63837
Catalog Number: E-AB-63837
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: WB
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: WB
Datasheet, Questions? Contact us!
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.
Research Area: Cancer, Epigenetics and Nuclear Signaling
Synonyms:
PABPN1, OPMD, PAB2, PABII, PABP-2, PABP2
Immunogen: A synthetic peptide of human PABPN1 (NP_004634.1).
Swissprot: Q86U42
Gene ID: 8106
Calculated MW: 31 kDa/32 kDa/37 kDa
Observed MW: 45 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:1000"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Cancer, Epigenetics and Nuclear Signaling
Synonyms:
PABPN1, OPMD, PAB2, PABII, PABP-2, PABP2
Immunogen: A synthetic peptide of human PABPN1 (NP_004634.1).
Swissprot: Q86U42
Gene ID: 8106
Calculated MW: 31 kDa/32 kDa/37 kDa
Observed MW: 45 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:1000"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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