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IDUA antibody (AA 1-87) (FITC)

This Rabbit Polyclonal antibody specifically detects IDUA in FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7999065
$570.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for IDUA antibody (AA 1-87) (FITC) (ABIN7999065)

Target

See all IDUA Antibodies
IDUA (Iduronidase, alpha-L- (IDUA))

Reactivity

  • 50
  • 26
  • 16
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 47
  • 2
  • 2
Rabbit

Clonality

  • 49
  • 2
Polyclonal

Conjugate

  • 25
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IDUA antibody is conjugated to FITC

Application

  • 31
  • 23
  • 19
  • 17
  • 4
  • 3
  • 3
  • 1
  • 1
Flow Cytometry (FACS)
  • Binding Specificity

    • 11
    • 9
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-87

    Purpose

    Anti-IDUA Antibody FITC Conjugated

    Cross-Reactivity (Details)

    No cross reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human INSIG1 recombinant protein (Position: M1-R87).

    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

    IDUA (Iduronidase, alpha-L- (IDUA))

    Alternative Name

    IDUA

    Background

    Background: This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I).

    Gene Full Name: alpha-L-iduronidase

    Gene ID

    3425

    UniProt

    P35475

    Pathways

    Glycosaminoglycan Metabolic Process
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