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Anti-IDS / Iduronate 2 Sulfatase Antibody (aa26-550, Biotin) LS-C68339

Catalog Size Price
LS-C68339-50 50 µg Unavailable

Most Popular IDS / Iduronate 2 Sulfatase Antibodies

Anti-IDS / Iduronate 2 Sulfatase Antibody (aa26-550) LS-C36844
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Anti-IDS / Iduronate 2 Sulfatase Antibody (aa26-550, Biotin) LS-C68339
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Anti-IDS / Iduronate 2 Sulfatase Antibody (aa440-451) IHC-plus™ LS-B8302
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Anti-IDS / Iduronate 2 Sulfatase Antibody (aa154-203) IHC-plus™ LS-B11028
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Anti-IDS / Iduronate 2 Sulfatase Antibody (clone 3B10) IHC-plus™ LS-B12191
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100% Guaranteed
Goat Polyclonal (IgG) to Human IDS / Iduronate 2 Sulfatase
Western blot
Biotin Conjugated


Human IDS / Iduronate 2 Sulfatase
Human (tested or 100% immunogen sequence identity)
IgG Polyclonal
Immunoaffinity purified


Western blot (0.1 - 0.2 µg/ml)

Specificity and Use

NS0-derived recombinant human rhIDS (aa 26-550).
Recognizes human IDS. Cross-reactivity: 50% with rmIDS.
Western Blot: 0.1-0.2 ug/ml. The detection limit is ~20 ng/lane under reducing and non-reducing conditions. The applications listed have been tested for the unconjugated form of this product. Other forms have not been tested.


Lyophilized, PBS, BSA.
250 ul sterile PBS
Store at -20°C prior to reconstitution. After reconstitution aliquot and freeze at-20°C. Avoid frequent freeze thaws.
For research use only.

About IDS / Iduronate 2 Sulfatase

P22304 NM_000202 NP_000193.1

IDS Antibody, Idursulfase Antibody, SIDS Antibody, Iduronate 2-sulfatase Antibody, MPS2 Antibody

Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. Iduronate-2-sulfatase has a strong sequence homology with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. A splice variant of this gene has been described.

Requested From: 
Date Requested: 8/20/2017

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