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Cofilin 2 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects Cofilin 2 in WB and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN5534069

Quick Overview for Cofilin 2 antibody (N-Term) (ABIN5534069)

Target

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

Reactivity

  • 49
  • 23
  • 9
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  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 46
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  • 1
Rabbit

Clonality

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Polyclonal

Conjugate

  • 32
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This Cofilin 2 antibody is un-conjugated

Application

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  • 10
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  • 2
  • 2
  • 1
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 10
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    • 1
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    AA 25-54, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This CFL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 25-54 amino acids from the N-terminal region of human CFL2.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    For IHC-P starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    Cofilin 2 (CFL2)

    Alternative Name

    CFL2

    Background

    This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. 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.

    Molecular Weight

    19 kDa

    Gene ID

    1073

    UniProt

    Q9Y281

    Pathways

    Caspase Cascade in Apoptosis
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