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MAGE-Like 2 antibody (AA 578-847)

This Rabbit Polyclonal antibody specifically detects MAGE-Like 2 in ELISA, WB, IHC (p) and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7875833
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for MAGE-Like 2 antibody (AA 578-847) (ABIN7875833)

Target

See all MAGE-Like 2 (MAGEL2) Antibodies
MAGE-Like 2 (MAGEL2)

Reactivity

  • 34
  • 2
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 34
  • 1
Rabbit

Clonality

  • 34
  • 1
Polyclonal

Conjugate

  • 10
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MAGE-Like 2 antibody is un-conjugated

Application

  • 13
  • 13
  • 11
  • 8
  • 8
  • 5
  • 3
  • 1
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 8
    • 3
    • 1
    • 1
    AA 578-847

    Purpose

    MAGEL2 Antibody / MAGE-like protein 2

    Purification

    Antigen affinity purified

    Immunogen

    An E.coli-derived human recombinant protein (amino acids Q578-A847) was used as the immunogen for the MAGEL2 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the MAGEL2 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 MAGEL2 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

    MAGE-Like 2 (MAGEL2)

    Alternative Name

    MAGEL2

    Background

    Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS.

    UniProt

    Q9UJ55
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