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Emerin antibody

This Rabbit Polyclonal antibody specifically detects Emerin in WB, IHC and IF. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN6989782
-15% Promotion 2026
$326.93
$384.62
save $57.69 (-15 %)
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 8 to 11 Business Days

Quick Overview for Emerin antibody (ABIN6989782)

Target

See all Emerin (EMD) Antibodies
Emerin (EMD)

Reactivity

  • 89
  • 26
  • 24
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 61
  • 28
  • 2
Rabbit

Clonality

  • 50
  • 41
Polyclonal

Conjugate

  • 41
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Emerin antibody is un-conjugated

Application

  • 78
  • 40
  • 34
  • 18
  • 17
  • 15
  • 13
  • 13
  • 8
  • 8
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Mouse

    Purification

    Purified by Protein A.

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human EMD (NP_000108.1).

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC()
    IF()

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C for 12 months.

    Expiry Date

    12 months
  • Target

    Emerin (EMD)

    Alternative Name

    EMD

    Background

    Synonyms: EMD,EDMD,LEMD5,STA,emerin

    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.

    Gene ID

    2010

    UniProt

    P50402
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