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IDUA antibody

This anti-IDUA antibody is a Rabbit Polyclonal antibody detecting IDUA in ELISA and WB. Suitable for Human and Mouse.
Catalog No. ABIN7229020

Quick Overview for IDUA antibody (ABIN7229020)

Target

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

Reactivity

  • 36
  • 14
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 33
  • 2
  • 2
Rabbit

Clonality

  • 35
  • 2
Polyclonal

Conjugate

  • 20
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IDUA antibody is un-conjugated

Application

  • 24
  • 18
  • 14
  • 9
  • 3
  • 2
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB)
  • Purpose

    IDUA Polyclonal Antibody

    Specificity

    The antibody detects endogenous levels of IDUA protein

    Purification

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    Immunogen

    Synthesized peptide derived from part region of human IDUA protein

    Isotype

    IgG
  • Application Notes

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    Comment

    Primary Antibody

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • Target

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

    Alternative Name

    IDUA

    Background

    Rabbit Anti-IDUA Polyclonal Antibody,Alpha-L-iduronidase,IDUA 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).,IDUA

    Molecular Weight

    observerd band 71kDa

    Gene ID

    3425

    UniProt

    P35475

    Pathways

    Glycosaminoglycan Metabolic Process
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