Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

IDUA antibody (AA 28-634)

This Rabbit Polyclonal antibody specifically detects IDUA in ELISA, WB, FACS, IHC (p) and IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7873280
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for IDUA antibody (AA 28-634) (ABIN7873280)

Target

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

Reactivity

  • 39
  • 15
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 36
  • 2
  • 2
Rabbit

Clonality

  • 38
  • 2
Polyclonal

Conjugate

  • 23
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IDUA antibody is un-conjugated

Application

  • 27
  • 19
  • 14
  • 10
  • 3
  • 3
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • Binding Specificity

    • 9
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 28-634

    Purpose

    IDUA Antibody / Alpha-L-iduronidase

    Purification

    Antigen affinity purified

    Immunogen

    An E.coli-derived human recombinant protein (amino acids A28-D634) was used as the immunogen for the IDUA antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the IDUA 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 IDUA 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

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

    Alternative Name

    IDUA

    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).

    UniProt

    P35475

    Pathways

    Glycosaminoglycan Metabolic Process
You are here:
Chat with us!