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Cofilin 2 antibody

This Mouse Monoclonal antibody specifically detects Cofilin 2 in WB, IF, IHC (p), ICC and FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7880465
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Cofilin 2 antibody (ABIN7880465)

Target

See all Cofilin 2 (CFL2) Antibodies
Cofilin 2 (CFL2)

Reactivity

  • 55
  • 24
  • 10
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 48
  • 6
  • 1
Mouse

Clonality

  • 49
  • 6
Monoclonal

Conjugate

  • 38
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Cofilin 2 antibody is un-conjugated

Application

  • 36
  • 21
  • 15
  • 15
  • 10
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Flow Cytometry (FACS)

Clone

8C13
  • Purpose

    Cofilin 2 Antibody / CFL2

    Sequence

    KDAIKKKFTG IKHEWQVNGL DDIKDRSTLG EKL

    Purification

    Affinity purified

    Immunogen

    Amino acids KDAIKKKFTGIKHEWQVNGLDDIKDRSTLGEKL were used as the immunogen for the Cofilin 2 antibody.

    Isotype

    IgG2b
  • Application Notes

    Optimal dilution of the Cofilin 2 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 Cofilin 2 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

    Cofilin 2 (CFL2)

    Alternative Name

    Cofilin 2

    Background

    Cofilin 2 (muscle), also known as CFL2, is a protein which in humans is encoded by the CFL2 gene. It is mapped to 14q12. This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. And this protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH -dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants.

    UniProt

    Q9Y281

    Pathways

    Caspase Cascade in Apoptosis
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