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SPG20 Antikörper (C-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SPG20 in WB und EIA. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN954907

Kurzübersicht für SPG20 Antikörper (C-Term) (ABIN954907)

Target

Alle SPG20 Antikörper anzeigen
SPG20 (Spastic Paraplegia 20 (Troyer Syndrome) (SPG20))

Reaktivität

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

Wirt

  • 24
Kaninchen

Klonalität

  • 24
Polyklonal

Konjugat

  • 14
  • 2
  • 2
  • 2
  • 2
  • 2
Dieser SPG20 Antikörper ist unkonjugiert

Applikation

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

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

    Spezifität

    This antibody recognizes Human

    Aufreinigung

    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

    Isotyp

    Ig Fraction
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.25 mg/mL

    Buffer

    PBS, 0.09 % Sodium Azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Handhabung

    Avoid repeated freezing and thawing.
  • Target

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

    Andere Bezeichnung

    Spartin / SPG20

    Hintergrund

    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

    Molekulargewicht

    72833 Da

    Gen-ID

    23111

    NCBI Accession

    NP_001135766

    Pathways

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