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Lamin B Receptor antibody (AA 102-209)

This Rabbit Polyclonal antibody specifically detects Lamin B Receptor in WB, ELISA, IF, FACS and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7869911
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Lamin B Receptor antibody (AA 102-209) (ABIN7869911)

Target

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

Reactivity

  • 45
  • 20
  • 13
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 43
  • 2
Rabbit

Clonality

  • 33
  • 12
Polyclonal

Conjugate

  • 15
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Lamin B Receptor antibody is un-conjugated

Application

  • 38
  • 16
  • 16
  • 14
  • 12
  • 12
  • 8
  • 4
Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 16
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 102-209

    Purpose

    LBR Antibody / Lamin B Receptor

    Purification

    Affinity purified

    Immunogen

    Amino acids H102-F209 from the human protein were used as the immunogen for the LBR antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the LBR 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

    -20 °C

    Storage Comment

    Store the LBR antibody at -20oC.
  • Target

    Lamin B Receptor (LBR)

    Alternative Name

    LBR

    Background

    Lamin-B receptor is a protein, and in humans, it is encoded by the LBR gene. It is mapped to 1q42.12. The protein encoded by this gene belongs to the ERG4/ERG24 family. It 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.

    UniProt

    Q14739
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