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DGCR2 antibody (AA 58-474) (Fluoro647)

The Rabbit Polyclonal anti-DGCR2 antibody is suitable to detect DGCR2 in samples from Human, Mouse and Rat. It has been validated for FACS.
Catalog No. ABIN7985233
$670.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for DGCR2 antibody (AA 58-474) (Fluoro647) (ABIN7985233)

Target

See all DGCR2 (DGS2) Antibodies
DGCR2 (DGS2) (DiGeorge Syndrome Chromosome Region-2 (DGS2))

Reactivity

  • 30
  • 28
  • 19
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 30
Rabbit

Clonality

  • 30
Polyclonal

Conjugate

  • 16
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This DGCR2 antibody is conjugated to Fluoro647

Application

  • 22
  • 14
  • 9
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 11
    • 7
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 58-474

    Purpose

    Anti-DGCR2 Antibody Fluoro647 Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human DGCR2 recombinant protein (Position: E58-E474).

    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

    DGCR2 (DGS2) (DiGeorge Syndrome Chromosome Region-2 (DGS2))

    Alternative Name

    DGCR2

    Background

    Background: Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.

    Gene Full Name: DiGeorge syndrome critical region gene 2

    Gene ID

    9993

    UniProt

    P98153
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