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Emerin antibody (AA 1-222)

This anti-Emerin antibody is a Mouse Monoclonal antibody detecting Emerin in ELISA, IHC, FACS and ICC. Suitable for Human.
Catalog No. ABIN5542309

Quick Overview for Emerin antibody (AA 1-222) (ABIN5542309)

Target

See all Emerin (EMD) Antibodies
Emerin (EMD)

Reactivity

  • 82
  • 17
  • 14
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 51
  • 31
  • 2
Mouse

Clonality

  • 50
  • 34
Monoclonal

Conjugate

  • 41
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Emerin antibody is un-conjugated

Application

  • 71
  • 33
  • 28
  • 20
  • 15
  • 13
  • 13
  • 8
  • 7
  • 7
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC)

Clone

8F5A8
  • Binding Specificity

    • 24
    • 15
    • 8
    • 8
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-222

    Purpose

    EMD Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human EMD (AA: 1-222) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    Emerin (EMD)

    Alternative Name

    EMD

    Background

    Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.

    Molecular Weight

    29 kDa

    UniProt

    P50402
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