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Myotilin antibody

This anti-Myotilin antibody is a Rabbit Polyclonal antibody detecting Myotilin in WB and IHC (p). Suitable for Human.
Catalog No. ABIN7465502

Quick Overview for Myotilin antibody (ABIN7465502)

Target

See all Myotilin (MYOT) Antibodies
Myotilin (MYOT)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Myotilin antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Myotilin. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: A549

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    Myotilin (MYOT)

    Alternative Name

    myotilin

    Background

    Myotilin , LGMD1 , LGMD1A , MFM3 , TTID , TTOD,This gene encodes a cystoskeletal protein which plays a significant role in the stability of thin filaments during muscle contraction. This protein binds F-actin, crosslinks actin filaments, and prevents latrunculin A-induced filament disassembly. Mutations in this gene have been associated with limb-girdle muscular dystrophy and myofibrillar myopathies. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.

    Molecular Weight

    55 kDa

    Gene ID

    9499

    UniProt

    Q9UBF9
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