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IDUA Polyclonal antibody

IDUA Polyclonal Antibody for WB, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, IP, ELISA

Alpha L iduronidase, IDA, IDUA, iduronidase, alpha L, MPS1

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 
SKU: 

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Quantity

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Tested Applications

Positive WB detected inmouse brain tissue, rat brain tissue
Positive IHC detected inhuman prostate cancer tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:1000-1:8000
Immunohistochemistry (IHC)IHC : 1:200-1:800
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

55158-1-AP targets IDUA in WB, IHC, IP, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

Peptide

Predict reactive species
Full Name iduronidase, alpha-L-
Calculated Molecular Weight 73 kDa
Observed Molecular Weight 73 kDa
GenBank Accession NumberNM_000203
Gene Symbol IDUA
Gene ID (NCBI) 3425
RRIDAB_11182946
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDP35475
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

IDUA belongs to the glycosyl hydrolase 39 family. It hydrolysis of unsulfated alpha-L-iduronosidic linkages in dermatan sulfate. Defects in IDUA are the cause of mucopolysaccharidosis type 1H (MPS1H)( also known as Hurler syndrome), MPS1H/S(also known as Hurler-Scheie syndrome) and MPS1S(also known as Scheie syndrome), which are rare lysosomal storage diseases. This antibody is specific to IDUA.

Protocols

Product Specific Protocols
IHC protocol for IDUA antibody 55158-1-APDownload protocol
WB protocol for IDUA antibody 55158-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

What published studies show

The IDUA Polyclonal antibody (Cat# 55158-1-AP) has 5 citations published in Mol Ther, Front Immunol, Mol Ther Methods Clin Dev, Mol Cell Biochem, and Hum Gene Ther. Research fields span liver-directed gene therapy for mucopolysaccharidosis type I-H (Hurler syndrome), renal clear cell carcinoma immunotherapy response prediction, and bone mineral density regulation. Applications cited include WB, IHC, IP, and ELISA in human and mouse species.

SpeciesApplicationTitle
mouseELISA

Mol Ther

Comparative evaluation of liver-directed knockin strategies with viral and nonviral vectors in mouse inherited disease models.

Authors - Xiu Jin
humanWB,IHC

Front Immunol

Leveraging diverse cell-death related signature predicts the prognosis and immunotherapy response in renal clear cell carcinoma

Authors - Zhengqi Wu
humanWB

Mol Ther Methods Clin Dev

Liver-directed gene therapy corrects neurologic disease in a murine model of mucopolysaccharidosis type I-Hurler.

Authors - Xiu Jin
IP

Mol Cell Biochem

Why SNP rs3755955 is associated with human bone mineral density? A molecular and cellular study in bone cells.

Authors - Pei He
humanWB,ELISA

Hum Gene Ther

Lipid Nanoparticle-Delivered mRNA Therapy Corrects Neonatal Murine MPS I-H.

Authors - Jiamei Fu
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