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Lamin B Receptor antibody (Middle Region)

The Rabbit Polyclonal anti-Lamin B Receptor antibody has been validated for WB. It is suitable to detect Lamin B Receptor in samples from Human.
Catalog No. ABIN635330

Quick Overview for Lamin B Receptor antibody (Middle Region) (ABIN635330)

Target

See all Lamin B Receptor (LBR) Antibodies
Lamin B Receptor (LBR)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Lamin B Receptor antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    Middle Region

    Specificity

    Lamin B Receptor antibody was raised against the middle region of LBR

    Purification

    Affinity purified

    Immunogen

    Lamin B Receptor antibody was raised using the middle region of LBR corresponding to a region with amino acids GANSQKNAFRKNPSDPKLAHLKTIHTSTGKNLLVSGWWGFVRHPNYLGDL
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    Lamin B Receptor Blocking Peptide, (ABIN938550), is also available for use as a blocking control in assays to test for specificity of this Lamin B Receptor antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of LBR antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    Lamin B Receptor (LBR)

    Alternative Name

    Lamin B Receptor

    Background

    The protein encoded by this gene belongs to the ERG4/ERG24 family. It is localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.

    Molecular Weight

    71 kDa (MW of target protein)
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