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EYA1 Antikörper (N-Term)

Dieses Anti-EYA1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von EYA1 in WB. Geeignet für Maus.
Produktnummer ABIN656379

Kurzübersicht für EYA1 Antikörper (N-Term) (ABIN656379)

Target

Alle EYA1 Antikörper anzeigen
EYA1 (Eyes Absent Homolog 1 (EYA1))

Reaktivität

  • 35
  • 18
  • 8
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
Maus

Wirt

  • 39
  • 1
  • 1
Kaninchen

Klonalität

  • 41
Polyklonal

Konjugat

  • 18
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser EYA1 Antikörper ist unkonjugiert

Applikation

  • 21
  • 18
  • 13
  • 13
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Klon

RB31192
  • Bindungsspezifität

    • 15
    • 9
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Aufreinigung

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

    Immunogen

    This EYA1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human EYA1.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody 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

    EYA1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Haltbarkeit

    6 months
  • Target

    EYA1 (Eyes Absent Homolog 1 (EYA1))

    Andere Bezeichnung

    EYA1

    Hintergrund

    This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Four transcript variants encoding three distinct isoforms have been identified for this gene.

    Molekulargewicht

    64593

    Gen-ID

    2138

    NCBI Accession

    NP_000494, NP_742055, NP_742056, NP_742057

    UniProt

    Q99502

    Pathways

    Sensory Perception of Sound, Positive Regulation of Response to DNA Damage Stimulus
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