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SGSH antibody (AA 206-502) (HRP)

The Rabbit Polyclonal anti-SGSH antibody is suitable to detect SGSH in samples from Human, Mouse and Rat. It has been validated for WB, IHC and ELISA.
Catalog No. ABIN8013234
$590.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for SGSH antibody (AA 206-502) (HRP) (ABIN8013234)

Target

See all SGSH Antibodies
SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))

Reactivity

  • 57
  • 17
  • 15
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
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Human, Mouse, Rat

Host

  • 54
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Rabbit

Clonality

  • 57
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Polyclonal

Conjugate

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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This SGSH antibody is conjugated to HRP

Application

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  • 5
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Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Binding Specificity

    • 15
    • 12
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    • 4
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    AA 206-502

    Purpose

    Anti-HSS/SGSH Antibody HRP Conjugated

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human HSS/SGSH recombinant protein (Position: R206-L502).

    Isotype

    IgG
  • Application Notes

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    Storage

    -20 °C

    Storage Comment

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    Expiry Date

    12 months
  • Target

    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))

    Alternative Name

    SGSH

    Background

    Background: N-sulphoglucosamine sulphohydrolase is an enzyme that in humans is encoded by the SGSH gene. This gene encodes the enzyme sulfamidase, one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.

    Gene Full Name: N-sulfoglucosamine sulfohydrolase

    Gene ID

    6448

    UniProt

    P51688

    Pathways

    Glycosaminoglycan Metabolic Process
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