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Tmc2 antibody

The Rabbit Polyclonal anti-Tmc2 antibody has been validated for ELISA and WB. It is suitable to detect Tmc2 in samples from Human, Mouse and Rat.
Catalog No. ABIN2463326

Quick Overview for Tmc2 antibody (ABIN2463326)

Target

See all Tmc2 Antibodies
Tmc2 (Transmembrane Channel-Like 2 (Tmc2))

Reactivity

  • 8
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 8
Rabbit

Clonality

  • 8
Polyclonal

Conjugate

  • 4
  • 2
  • 1
  • 1
This Tmc2 antibody is un-conjugated

Application

  • 4
  • 3
  • 1
ELISA, Western Blotting (WB)
  • Purification

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TMC2.
  • Application Notes

    TMC2 antibody can be used for detection of TMC2 by ELISA at 1:1562500. TMC2 antibody can be used for detection of TMC2 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handling Advice

    As with any antibody avoid repeat freeze-thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store TMC2 antibody at -20 °C.
  • Target

    Tmc2 (Transmembrane Channel-Like 2 (Tmc2))

    Alternative Name

    TMC2

    Background

    TMC2 is considered a member of transmembrane proteins family. The specific function of this gene is unknown, however, expression in the inner ear suggests that it may be crucial for normal auditory function. This gene is considered a member of a gene family predicted to encode transmembrane proteins. The specific function of this gene is unknown, however, expression in the inner ear suggests that it may be crucial for normal auditory function. Mutations in this gene may underlie hereditary disorders of balance and hearing.

    Molecular Weight

    102 kDa

    Gene ID

    117532

    NCBI Accession

    NP_542789

    UniProt

    Q8TDI7
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