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Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2) (Middle Region) Peptid

ALS2 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN973149
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 15 bis 22 Werktagen

Kurzübersicht für Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2) (Middle Region) Peptid (ABIN973149)

Target

ALS2 (Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2))

Spezies

Human

Quelle

  • 2
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Sequenz

    ALRGMSDLPP YGSGSSVQRQ EPPISRSAKY TFYKDPRLKD ATYDGRWLSG

    Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti-ALS2 Antibody(ARP57487_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Aufreinigung

    Purified
  • Applikationshinweise

    Each Investigator should determine their own optimal working dilution for specific applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    ALS2 (Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2))

    Hintergrund

    The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene.

    Alias Symbols: ALS2CR6, ALSJ, FLJ31851, IAHSP, KIAA1563, MGC87187, PLSJ

    Protein Interaction Partner: YWHAB

    Protein Size: 1657

    Molekulargewicht

    184 kDa

    Gen-ID

    57679

    NCBI Accession

    NM_020919, NP_065970

    UniProt

    Q96Q42
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