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EPHX2 antibody (AA 505-543)

The Rabbit Polyclonal anti-EPHX2 antibody is suitable to detect EPHX2 in samples from Human, Mouse and Rat. It has been validated for WB and FACS.
Catalog No. ABIN5647426
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for EPHX2 antibody (AA 505-543) (ABIN5647426)

Target

See all EPHX2 Antibodies
EPHX2 (Epoxide Hydrolase 2, Cytoplasmic (EPHX2))

Reactivity

  • 33
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 25
  • 6
  • 2
  • 1
Rabbit

Clonality

  • 24
  • 10
Polyclonal

Conjugate

  • 30
  • 2
  • 1
  • 1
This EPHX2 antibody is un-conjugated

Application

  • 20
  • 14
  • 12
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Binding Specificity

    • 8
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 505-543

    Purpose

    EPHX2 Antibody

    Purification

    Antigen affinity

    Immunogen

    Amino acids 505-543 (QHMEDWIPHLKRGHIEDCGHWTQMDKPTEVNQILIKWLD-human) were used as the immunogen for the EPHX2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the EPHX2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the EPHX2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    EPHX2 (Epoxide Hydrolase 2, Cytoplasmic (EPHX2))

    Alternative Name

    EPHX2

    Background

    Soluble epoxide hydrolase (sEH), or Epoxide hydrolase 2, is a bifunctional enzyme that in humans is encoded by the EPHX2 gene. It is mapped to 8p21.2-p21.1. This gene encodes a member of the epoxide hydrolase family. The protein, found in both the cytosol and peroxisomes, binds to specific epoxides and converts them to the corresponding dihydrodiols. Mutations in this gene have been associated with familial hypercholesterolemia. Alternatively spliced transcript variants have been described.

    Gene ID

    2053

    UniProt

    P34913
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