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Anti-IDS / Iduronate 2 Sulfatase Antibody (aa26-550) LS-C36844

Ordering

Wt. Vol. Conc. Price
100 µg 500 µl 0.2 mg/ml $695
Inquire for larger quantities

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Most Popular IDS / Iduronate 2 Sulfatase Antibodies

Anti-IDS / Iduronate 2 Sulfatase Antibody (aa26-550) LS-C36844
Goat Polyclonal (IgG) to Human IDS / Iduronate 2 Sulfatase
Human
Western blot, Immunoprecipitation, ELISA
Unconjugated
Anti-IDS / Iduronate 2 Sulfatase Antibody (aa26-550, Biotin) LS-C68339
Goat Polyclonal (IgG) to Human IDS / Iduronate 2 Sulfatase
Human
Western blot
Biotin Conjugated

100% Guaranteed 100% Guaranteed
Goat Polyclonal (IgG) to Human IDS / Iduronate 2 Sulfatase
Human
Western blot, Immunoprecipitation, ELISA
Unconjugated

Details

Human IDS / Iduronate 2 Sulfatase
Goat
Human (tested or 100% immunogen sequence identity)
IgG Polyclonal
Unconjugated
Affinity purified
Unmodified

Applications

  • Western blot
  • Immunoprecipitation
  • ELISA

Specificity and Use

IDS / Iduronate 2 Sulfatase antibody was raised against nS0-derived rhIDS (aa26-550).
aa26-550
Selected for its ability to recognize human IDS in direct ELISAs and Western Blots. In these formats, this antibody shows ~50% cross-reactivity with rmIDS.
Western Blot: This antibody can be used at 0.1-0.2 ug/mL with the appropriate secondary reagents to detect human IDS. The detection limit for rhIDS is approximately 25 ng/lane under non-reducing and reducing conditions. Immunoprecipitation: This antibody has been used to immunoprecipitate rhIDS from conditioned media of transfected NS0 cells. The recovered rhIDS can be detected by Western Blot analysis. Direct ELISA: This antibody can be used at 0.5-1.0 ug/mL with the appropriate secondary reagents to detect human IDS. The detection limit for rhIDS is approximately 0.3 ng/well.

Packaging

Lyophilized from PBS, pH 7.4, 5% trehalose
500 µl Reconstitute with 500ul sterile PBS
Store at -20°C. After reconstitution, aliquot and store at -20°C. Avoid freeze/thaw cycles.
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: United States
Date Requested: 12/3/2016

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