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FKRP Antikörper (AA 237-265)

Dieses Anti-FKRP-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von FKRP in WB. Geeignet für Human.
Produktnummer ABIN5536570

Kurzübersicht für FKRP Antikörper (AA 237-265) (ABIN5536570)

Target

Alle FKRP Antikörper anzeigen
FKRP (Fukutin Related Protein (FKRP))

Reaktivität

  • 40
  • 15
  • 14
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 32
  • 8
Kaninchen

Klonalität

  • 32
  • 8
Polyklonal

Konjugat

  • 18
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FKRP Antikörper ist unkonjugiert

Applikation

  • 26
  • 26
  • 5
  • 4
  • 2
Western Blotting (WB)
  • Bindungsspezifität

    • 10
    • 6
    • 6
    • 6
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 237-265

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This FKRP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 237-265 amino acids from the Central region of human FKRP.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    For WB starting dilution is: 1:1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    FKRP (Fukutin Related Protein (FKRP))

    Andere Bezeichnung

    FKRP

    Hintergrund

    This gene encodes a protein which is targeted to the medial Golgi apparatus and is necessary for posttranslational modification of dystroglycan. Mutations in this gene have been associated with congenital muscular dystrophy, mental retardation, and cerebellar cysts. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq].

    Molekulargewicht

    55 kDa

    Gen-ID

    79147

    UniProt

    Q9H9S5

    Pathways

    Regulation of Carbohydrate Metabolic Process
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