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IDUA antibody (AA 101-200)

The Rabbit Polyclonal anti-IDUA antibody has been validated for ELISA and WB. It is suitable to detect IDUA in samples from Rat.
Catalog No. ABIN1713845

Quick Overview for IDUA antibody (AA 101-200) (ABIN1713845)

Target

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

Reactivity

  • 38
  • 14
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Rat

Host

  • 33
  • 3
  • 2
Rabbit

Clonality

  • 35
  • 3
Polyclonal

Conjugate

  • 21
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IDUA antibody is un-conjugated

Application

  • 25
  • 18
  • 17
  • 9
  • 5
  • 3
  • 2
  • 1
  • 1
ELISA, Western Blotting (WB)
  • Binding Specificity

    • 8
    • 6
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 101-200

    Cross-Reactivity

    Rat

    Predicted Reactivity

    Human,Mouse

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human IDUA

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    IDUA

    Background

    Synonyms: IDA, MPS1, Alpha-L-iduronidase, 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). [provided by RefSeq, Jul 2008].

    Gene ID

    3425

    UniProt

    P35475

    Pathways

    Glycosaminoglycan Metabolic Process
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