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POLE3 antibody (full length)

The Mouse Monoclonal anti-POLE3 antibody is suitable to detect POLE3 in samples from Human. It has been validated for IF, FACS and ELISA.
Catalog No. ABIN7878828
$317.38
Plus shipping costs $50.00
20 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for POLE3 antibody (full length) (ABIN7878828)

Target

See all POLE3 Antibodies
POLE3 (Polymerase (DNA Directed), epsilon 3 (p17 Subunit) (POLE3))

Reactivity

  • 46
  • 19
  • 15
  • 5
  • 5
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 35
  • 11
Mouse

Clonality

  • 38
  • 8
Monoclonal

Conjugate

  • 32
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This POLE3 antibody is un-conjugated

Application

  • 24
  • 15
  • 10
  • 8
  • 7
  • 4
  • 4
  • 2
  • 1
  • 1
Immunofluorescence (IF), Flow Cytometry (FACS), ELISA

Clone

PCRP-POLE3-3D3
  • Binding Specificity

    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    full length

    Purpose

    CHRAC17 Antibody / POLE3

    Purification

    Protein A/G affinity

    Immunogen

    Recombinant full-length human POLE3 protein was used as the immunogen for the CHRAC17 antibody.

    Isotype

    IgG2a
  • Application Notes

    Optimal dilution of the CHRAC17 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.2 mg/mL

    Buffer

    0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

    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

    Aliquot the CHRAC17 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • Target

    POLE3 (Polymerase (DNA Directed), epsilon 3 (p17 Subunit) (POLE3))

    Alternative Name

    CHRAC17

    Background

    DNA replication is initiated by the binding of initiation factors to the origin of replication. Nucleosomes inhibit access to the replication machinery at these origin sequences. Nucleosome remodeling factors increase the accessibility of nucleosomal DNA to transcriptional regulators. CHRAC15 and CHRAC17 are subunits of the nucleosomal remodeling factor CHRAC (chromatin accessibility complex), which increases the accessibility of nucleosomal DNA in an ATP-dependent manner. Unlike other known chromatin remodeling factors, CHRAC also functions during chromatin assembly by using ATP to convert irregular chromatin into a regular array of nucleosomes with even spacing. This conversion process occurs when CHRAC organizes randomly deposited histones into a regularly spaced array. In the presence of CHRAC, the nucleosomal ATPase ISWI catalyzes several ATP-dependent transitions of chromatin structure.

    UniProt

    Q9NRF9

    Pathways

    DNA Damage Repair
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