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Sacsin antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects Sacsin in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5673657
$483.54
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Quick Overview for Sacsin antibody (C-Term) (ABIN5673657)

Target

See all Sacsin (SACS) Antibodies
Sacsin (SACS) (Spastic Ataxia of Charlevoix-Saguenay (Sacsin) (SACS))

Reactivity

  • 11
  • 5
  • 1
Human

Host

  • 10
  • 1
Rabbit

Clonality

  • 11
Polyclonal

Conjugate

  • 7
  • 2
  • 1
  • 1
This Sacsin antibody is un-conjugated

Application

  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 5
    • 2
    • 1
    • 1
    • 1
    C-Term

    Sequence

    VVEQAWKLPE SERKKIIRRL YLKWHPDKNP ENHDIANEVF KHLQNEINRL

    Purification

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the C terminal region of human SACS
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    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.

    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

    Sacsin (SACS) (Spastic Ataxia of Charlevoix-Saguenay (Sacsin) (SACS))

    Alternative Name

    SACS

    Background

    This gene encodes the sacsin protein, which includes a UbL domain at the N-terminus, a DnaJ domain, and a HEPN domain at the C-terminus. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles and at low levels in the pancreas. This gene includes a very large exon spanning more than 12.8 kb. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. The authors of a publication on the effects of siRNA-mediated sacsin knockdown concluded that sacsin protects against mutant ataxin-1 and suggest that "the large multi-domain sacsin protein is able to recruit Hsp70 chaperone action and has the potential to regulate the effects of other ataxia proteins". A pseudogene associated with this gene is located on chromosome 11. Alternative splicing of this gene results in multiple transcript variants.

    Alias Symbols: SPAX6, ARSACS, DNAJC29, PPP1R138

    Protein Size: 309

    Gene ID

    26278

    NCBI Accession

    NM_014363, NP_055178

    UniProt

    Q7Z6W7
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