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GNS antibody (C-Term)

This anti-GNS antibody is a Rabbit Polyclonal antibody detecting GNS in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN635775

Quick Overview for GNS antibody (C-Term) (ABIN635775)

Target

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

Reactivity

  • 32
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse, Rat

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
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Specificity

    GNS antibody was raised against the C terminal of GNS

    Purification

    Affinity purified

    Immunogen

    GNS antibody was raised using the C terminal of GNS corresponding to a region with amino acids PILRGASNLTWRSDVLVEYQGEGRNVTDPTCPSLSPGVSQCFPDCVCEDA
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    GNS Blocking Peptide, (ABIN5613817), is also available for use as a blocking control in assays to test for specificity of this GNS antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of GNS antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 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, heparin sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder ucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

    Molecular Weight

    58 kDa (MW of target protein)

    Pathways

    Glycosaminoglycan Metabolic Process
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