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MYOZ2 antibody

The Rabbit Polyclonal anti-MYOZ2 antibody has been validated for ELISA and IHC. It is suitable to detect MYOZ2 in samples from Human and Mouse.
Catalog No. ABIN7246214

Quick Overview for MYOZ2 antibody (ABIN7246214)

Target

See all MYOZ2 Antibodies
MYOZ2 (Myozenin 2 (MYOZ2))

Reactivity

  • 33
  • 6
  • 3
  • 1
Human, Mouse

Host

  • 30
  • 4
Rabbit

Clonality

  • 31
  • 3
Polyclonal

Conjugate

  • 20
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MYOZ2 antibody is un-conjugated

Application

  • 24
  • 17
  • 5
  • 5
  • 2
  • 2
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Full length fusion protein

    Isotype

    IgG
  • Application Notes

    IHC 1:40-1:200, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.32 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    MYOZ2 (Myozenin 2 (MYOZ2))

    Alternative Name

    MYOZ2

    Background

    MYOZ2 (Myozenin 2) is a Protein Coding gene. Diseases associated with MYOZ2 include Cardiomyopathy, Hypertrophic, 16 and Myoz2-Related Familial Hypertrophic Cardiomyopathy. GO annotations related to this gene include actin binding and telethonin binding. An important paralog of this gene is MYOZ1.The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.

    UniProt

    Q9NPC6
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