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ERLIN2 antibody (AA 87-339)

This Mouse Monoclonal antibody specifically detects ERLIN2 in WB, IHC, ICC, FACS and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7602582

Quick Overview for ERLIN2 antibody (AA 87-339) (ABIN7602582)

Target

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

Reactivity

  • 35
  • 6
  • 5
  • 2
  • 2
  • 1
Human

Host

  • 31
  • 3
  • 1
Mouse

Clonality

  • 30
  • 5
Monoclonal

Conjugate

  • 25
  • 3
  • 3
  • 2
  • 1
  • 1
This ERLIN2 antibody is un-conjugated

Application

  • 29
  • 18
  • 15
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunocytochemistry (ICC), Flow Cytometry (FACS), Immunofluorescence (IF)

Clone

3H9A2
  • Binding Specificity

    • 10
    • 7
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    AA 87-339

    Purpose

    Anti-Erlin-2/ERLIN2 Antibody Picoband® (monoclonal, 3H9A2)

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-Erlin-2/ERLIN2 Antibody Picoband® (monoclonal, 3H9A2) (ABIN7602582). Tested in Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human Erlin-2/ERLIN2 recombinant protein (Position: D87-N339).

    Isotype

    IgG2b
  • Application Notes

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    1. Al-Saif, A., Bohlega, S., Al-Mohanna, F. Loss of ERLIN2 function leads to juvenile primary lateral sclerosis. Ann. Neurol. 72: 510-516, 2012. 2. Alazami, A. M., Adly, N., Al Dhalaan, H., Alkuraya, F. S. A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18). Neurogenetics 12: 333-336, 2011. 3. Browman, D. T., Resek, M. E., Zajchowski, L. D., Robbins, S. M. Erlin-1 and erlin-2 are novel members of the prohibitin family of proteins that define lipid-raft-like domains of the ER. J. Cell Sci. 119: 3149-3160, 2006.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    ERLIN2 (ER Lipid Raft Associated 2 (ERLIN2))

    Alternative Name

    ERLIN2

    Background

    Synonyms: T-complex protein 1 subunit gamma, TCP-1-gamma, CCT-gamma, hTRiC5, CCT3, CCTG, TRIC5

    Tissue Specificity: Ubiquitously expressed with highest levels in spleen, thymus and immature brain.

    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.

    Molecular Weight

    43 kDa

    Gene ID

    11160

    UniProt

    O94905
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