IDUA antibody

Catalog No. ABIN7245281

Product Details anti-IDUA Antibody

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IDUA antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Synthetic peptide of human IDUA

Isotype: IgG

Application Details

Application Notes: IHC 1:30-1:150, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.96 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for IDUA

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

Alternative Name: IDUA (IDUA Products)

Synonyms: IDA antibody, MPS1 antibody, 6030426D08 antibody, alpha-L-iduronidase antibody, MGC80842 antibody, si:ch211-12e13.9 antibody, IDUA antibody, iduronidase, alpha-L- antibody, iduronidase, alpha-L- L homeolog antibody, alpha-L-iduronidase antibody, IDUA antibody, Idua antibody, idua.L antibody, idua antibody, LOC5564727 antibody

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