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NAGLU antibody (AA 24-489) (Fluoro488)

This Rabbit Polyclonal antibody specifically detects NAGLU in FACS. It exhibits reactivity toward Mouse, Human and Rat.
Catalog No. ABIN8012987
$570.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for NAGLU antibody (AA 24-489) (Fluoro488) (ABIN8012987)

Target

See all NAGLU Antibodies
NAGLU (N-Acetylglucosaminidase, alpha (NAGLU))

Reactivity

  • 23
  • 18
  • 17
  • 1
  • 1
  • 1
Mouse, Human, Rat

Host

  • 27
  • 4
Rabbit

Clonality

  • 28
  • 3
Polyclonal

Conjugate

  • 18
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NAGLU antibody is conjugated to Fluoro488

Application

  • 23
  • 9
  • 8
  • 7
  • 5
  • 4
  • 1
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 12
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 24-489

    Purpose

    Anti-NAGLU Antibody Fluoro488 Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human NAGLU recombinant protein (Position: D24-D489).

    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

    NAGLU (N-Acetylglucosaminidase, alpha (NAGLU))

    Alternative Name

    NAGLU

    Background

    Background: N-acetylglucosaminidase, alpha is a protein that in humans is encoded by the NAGLU gene. This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate.

    Gene Full Name: N-acetyl-alpha-glucosaminidase

    Gene ID

    4669

    UniProt

    P54802

    Pathways

    Glycosaminoglycan Metabolic Process
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