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GNS antibody (AA 174-203)

The Rabbit Polyclonal anti-GNS antibody has been validated for WB and IHC (p). It is suitable to detect GNS in samples from Human.
Catalog No. ABIN390494

Quick Overview for GNS antibody (AA 174-203) (ABIN390494)

Target

See all GNS Antibodies
GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

Reactivity

  • 32
  • 8
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 29
  • 3
  • 1
Rabbit

Clonality

  • 32
  • 1
Polyclonal

Conjugate

  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GNS antibody is un-conjugated

Application

  • 16
  • 13
  • 13
  • 11
  • 6
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB19340
  • Binding Specificity

    • 15
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 174-203

    Predicted Reactivity

    B, M

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    Immunogen

    This GNS antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 174-203 amino acids from the Central region of human GNS.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. IHC-P: 1:50~100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

    Alternative Name

    GNS

    Background

    GNS is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

    Molecular Weight

    62082

    Gene ID

    2799

    NCBI Accession

    NP_002067

    UniProt

    P15586

    Pathways

    Glycosaminoglycan Metabolic Process
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