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SPG20 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects SPG20 in WB and EIA. It exhibits reactivity toward Human.
Catalog No. ABIN954907

Quick Overview for SPG20 antibody (C-Term) (ABIN954907)

Target

See all SPG20 Antibodies
SPG20 (Spastic Paraplegia 20 (Troyer Syndrome) (SPG20))

Reactivity

  • 24
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 24
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 14
  • 2
  • 2
  • 2
  • 2
  • 2
This SPG20 antibody is un-conjugated

Application

  • 23
  • 15
  • 9
  • 8
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 8
    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 490-519, C-Term

    Specificity

    This antibody recognizes Human

    Purification

    Affinity Chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 490-519 amino acids from the C-terminal region of Human SPG20 Genename: SPG20

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS, 0.09 % Sodium Azide

    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 repeated freezing and thawing.
  • Target

    SPG20 (Spastic Paraplegia 20 (Troyer Syndrome) (SPG20))

    Alternative Name

    Spartin / SPG20

    Background

    SPG20 is a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome)Synonyms: KIAA0610, Spastic paraplegia 20 protein, TAHCCP1, Trans-activated by hepatitis C virus core protein 1

    Molecular Weight

    72833 Da

    Gene ID

    23111

    NCBI Accession

    NP_001135766

    Pathways

    Regulation of Cell Size, SARS-CoV-2 Protein Interactome
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