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ERLIN2 antibody (AA 87-339)

The Mouse Monoclonal anti-ERLIN2 antibody (Clone 3H9A2) (ABIN7877017) specifically detects ERLIN2 in WB, IF, FACS and IHC (p). The antibody is reactive with Human samples.
Catalog No. ABIN7877017
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for ERLIN2 antibody (AA 87-339) (ABIN7877017)

Target

See all ERLIN2 Antibodies
ERLIN2 (ER Lipid Raft Associated 2 (ERLIN2))

Reactivity

  • 46
  • 19
  • 7
  • 2
  • 2
  • 1
Human

Host

  • 42
  • 3
  • 1
Mouse

Clonality

  • 31
  • 15
Monoclonal

Conjugate

  • 27
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ERLIN2 antibody is un-conjugated

Application

  • 40
  • 22
  • 18
  • 14
  • 13
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

3H9A2
  • Binding Specificity

    • 11
    • 7
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    AA 87-339

    Purpose

    ERLIN2 Antibody

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids D87-N339) was used as the immunogen for the ERLIN2 antibody.

    Isotype

    IgG2b
  • Application Notes

    Optimal dilution of the ERLIN2 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 ERLIN2 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

    ERLIN2 (ER Lipid Raft Associated 2 (ERLIN2))

    Alternative Name

    ERLIN2

    Background

    Erlin-2 is a protein that in humans is encoded by the ERLIN2 gene. This gene encodes a member of the SPFH domain-containing family of lipid raft-associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1,4,5-trisphosphate (IP3) signaling by mediating ER-associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia-18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

    UniProt

    O94905
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