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SHROOM2 antibody

The Rabbit Polyclonal anti-SHROOM2 antibody has been validated for ELISA and WB. It is suitable to detect SHROOM2 in samples from Human, Mouse and Rat.
Catalog No. ABIN2458127

Quick Overview for SHROOM2 antibody (ABIN2458127)

Target

See all SHROOM2 Antibodies
SHROOM2 (Shroom Family Member 2 (SHROOM2))

Reactivity

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Human, Mouse, Rat

Host

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Rabbit

Clonality

  • 40
Polyclonal

Conjugate

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This SHROOM2 antibody is un-conjugated

Application

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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 SHROOM2.
  • Application Notes

    SHROOM2 antibody can be used for detection of SHROOM2 by ELISA at 1:312500. SHROOM2 antibody can be used for detection of SHROOM2 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 SHROOM2 antibody at -20 °C.
  • Target

    SHROOM2 (Shroom Family Member 2 (SHROOM2))

    Alternative Name

    SHROOM2

    Background

    SHROOM2 shares significant similarities with the apical protein from Xenopus laevis which is implicated in amiloride-sensitive sodium channel activity. This gene is a strong candidate gene for ocular albinism type 1 syndrome.The protein encoded by this gene shares significant similarities with the apical protein from Xenopus laevis which is implicated in amiloride-sensitive sodium channel activity. This gene is a strong candidate gene for ocular albinism type 1 syndrome.

    Molecular Weight

    176 kDa

    Gene ID

    357

    NCBI Accession

    NP_001640

    UniProt

    Q13796

    Pathways

    Cell-Cell Junction Organization, Asymmetric Protein Localization
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