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PABPN1 antibody

This Rabbit Monoclonal antibody specifically detects PABPN1 in WB, IF and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN7269445

Quick Overview for PABPN1 antibody (ABIN7269445)

Target

See all PABPN1 Antibodies
PABPN1 (Poly A Binding Protein Nuclear 1 (PABPN1))

Reactivity

  • 30
  • 14
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
Human

Host

  • 30
Rabbit

Clonality

  • 19
  • 11
Monoclonal

Conjugate

  • 18
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PABPN1 antibody is un-conjugated

Application

  • 22
  • 8
  • 6
  • 6
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
  • Purpose

    PABPN1 Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human PABPN1

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000, IHC,1:50 - 1:200, IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    PABPN1 (Poly A Binding Protein Nuclear 1 (PABPN1))

    Alternative Name

    PABPN1

    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],OPMD, PAB2, PABII, PABP-2, PABP2,Epigenetics & Nuclear Signaling,RNA Binding,PABPN1

    Molecular Weight

    49kDa

    Gene ID

    8106

    UniProt

    Q86U42
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