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SPG7 antibody (AA 384-568)

The Rabbit Polyclonal anti-SPG7 antibody has been validated for WB. It is suitable to detect SPG7 in samples from Human.
Catalog No. ABIN1886423

Quick Overview for SPG7 antibody (AA 384-568) (ABIN1886423)

Target

See all SPG7 Antibodies
SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivity

  • 25
  • 5
  • 3
  • 3
  • 1
  • 1
Human

Host

  • 18
  • 10
Rabbit

Clonality

  • 20
  • 8
Polyclonal

Conjugate

  • 23
  • 1
  • 1
  • 1
  • 1
  • 1
This SPG7 antibody is un-conjugated

Application

  • 26
  • 11
  • 10
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 384-568

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 384 and 568 of SPG7
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Alternative Name

    SPG7

    Background

    This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is 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.Two transcript variants encoding distinct isoforms have been identified for this gene.Mutations associated with this gene cause autosomal recessive spastic paraplegia 7.[provided by RefSeq]

    Molecular Weight

    88 kDa

    Gene ID

    6687
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