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MAGE-Like 2 antibody (AA 578-847) (APC)

The APC-conjugated Rabbit Polyclonal anti-MAGE-Like 2 antibody (ABIN8007358) specifically detects MAGE-Like 2 in FACS. The antibody is reactive with Human samples.
Catalog No. ABIN8007358
$820.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for MAGE-Like 2 antibody (AA 578-847) (APC) (ABIN8007358)

Target

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

Reactivity

  • 45
  • 2
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 45
  • 1
Rabbit

Clonality

  • 45
  • 1
Polyclonal

Conjugate

  • 12
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 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 conjugated to APC

Application

  • 15
  • 13
  • 13
  • 12
  • 11
  • 10
  • 6
  • 3
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 12
    • 8
    • 3
    • 1
    AA 578-847

    Purpose

    Anti-MAGEL2 Antibody APC Conjugated

    Cross-Reactivity (Details)

    No cross reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human MAGEL2 recombinant protein (Position: Q578-A847).

    Isotype

    IgG
  • Application Notes

    Flow Cytometry, Optimal dilutions should be determined by end users.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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

    -20 °C

    Storage Comment

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    Expiry Date

    12 months
  • Target

    MAGE-Like 2 (MAGEL2)

    Alternative Name

    MAGEL2

    Background

    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.

    Gene Full Name: MAGE family member L2

    Gene ID

    54551

    UniProt

    Q9UJ55
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