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HGSNAT antibody (N-Term)

This anti-HGSNAT antibody is a Rabbit Polyclonal antibody detecting HGSNAT in WB. Suitable for Human, Dog and Horse.
Catalog No. ABIN2790259

Quick Overview for HGSNAT antibody (N-Term) (ABIN2790259)

Target

See all HGSNAT Antibodies
HGSNAT (Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT))

Reactivity

  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Dog, Horse

Host

  • 3
Rabbit

Clonality

  • 3
Polyclonal

Conjugate

  • 3
This HGSNAT antibody is un-conjugated

Application

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

    • 1
    • 1
    N-Term

    Sequence

    RALAALLLAA SVLSAALLAP GGSSGRDAQA APPRDLDKKR HAELKMDQAL

    Predicted Reactivity

    Dog: 86%, Horse: 82%, Human: 100%

    Characteristics

    This is a rabbit polyclonal antibody against HGSNAT. It was validated on Western Blot.

    Purification

    Affinity Purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N-terminal region of Human HGSNAT
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeat freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    HGSNAT (Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT))

    Alternative Name

    HGSNAT

    Background

    This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate.
    Protein Size: 219

    Molecular Weight

    24 kDa

    Gene ID

    138050

    UniProt

    Q8IVU6

    Pathways

    Glycosaminoglycan Metabolic Process
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