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Spastin antibody

This Rabbit Polyclonal antibody specifically detects Spastin in ELISA and IHC. It exhibits reactivity toward Mouse, Rat and Human.
Catalog No. ABIN7243310

Quick Overview for Spastin antibody (ABIN7243310)

Target

See all Spastin (SPAST) Antibodies
Spastin (SPAST)

Reactivity

  • 36
  • 36
  • 26
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Mouse, Rat, Human

Host

  • 27
  • 15
Rabbit

Clonality

  • 26
  • 16
Polyclonal

Conjugate

  • 12
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Spastin antibody is un-conjugated

Application

  • 35
  • 14
  • 13
  • 13
  • 13
  • 8
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human SPAST

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Spastin (SPAST)

    Alternative Name

    SPAST

    Background

    This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The encoded ATPase may be involved in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full length sequences have not been determined. Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.

    NCBI Accession

    NP_055761

    UniProt

    Q9UBP0

    Pathways

    Microtubule Dynamics, M Phase, Regulation of Cell Size
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