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SHROOM2 antibody (AA 427-1138)

The Rabbit Polyclonal anti-SHROOM2 antibody is suitable to detect SHROOM2 in samples from Human. It has been validated for ELISA, WB and FACS.
Catalog No. ABIN7874940
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SHROOM2 antibody (AA 427-1138) (ABIN7874940)

Target

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

Reactivity

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Human

Host

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Rabbit

Clonality

  • 42
Polyclonal

Conjugate

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This SHROOM2 antibody is un-conjugated

Application

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ELISA, Western Blotting (WB), Flow Cytometry (FACS)
  • Binding Specificity

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    AA 427-1138

    Purpose

    SHROOM2 Antibody / APXL

    Purification

    Antigen affinity purified

    Immunogen

    E. coli-derived recombinant human protein (amino acids R427-H1138) was used as the immunogen for the SHROOM2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the SHROOM2 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the SHROOM2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    SHROOM2 (Shroom Family Member 2 (SHROOM2))

    Alternative Name

    SHROOM2

    Background

    Shroom family member 2 is a protein that in humans is encoded by the SHROOM2 gene. This gene represents the human homolog of Xenopus laevis apical protein (APX) gene, which is implicated in amiloride-sensitive sodium channel activity. It is expressed in endothelial cells and facilitates the formation of a contractile network within endothelial cells. Depletion of this gene results in an increase in endothelial sprouting, migration, and angiogenesis. This gene is highly expressed in the retina, and is a strong candidate for ocular albinism type 1 syndrome. Alternatively spliced transcript variants have been found for this gene.

    UniProt

    Q13796

    Pathways

    Cell-Cell Junction Organization, Asymmetric Protein Localization
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