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Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12) Peptid

KCNJ12 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN939681

Kurzübersicht für Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12) Peptid (ABIN939681)

Target

Kir2.2 (KCNJ12) (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12))

Spezies

Säugetier

Quelle

  • 2
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein-Typ

    Synthetic

    Sequenz

    KDLVENKFLL PSANSFCYEN ELAFLSRDEE DEADGDQDGR SRDGLSPQAR

    Produktmerkmale

    A synthetic peptide for use as a blocking control in assays to test for specificity of KCNJ12 antibody,
    Alternative Names: KCNJ12 control peptide, KCNJ12 antibody Blocking Peptide, Anti-KCNJ12 Blocking Peptide, Potassium Inwardly-Rectifying Channel Subfamily J Member 12 Blocking Peptide, FLJ14167 Blocking Peptide, IRK2 Blocking Peptide, KCNJN1 Blocking Peptide, Kir2.2 Blocking Peptide, Kir2.2v Blocking Peptide, hIRK Blocking Peptide, hIRK1 Blocking Peptide, hkir2.2x Blocking Peptide, kcnj12x Blocking Peptide, KCNJ12, KCNJ-12, KCNJ 12, KCNJ-12 Blocking Peptide, KCNJ 12 Blocking Peptide
  • Applikationshinweise

    Optimal conditions should be determined by the investigator

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20 °C long term.
  • Target

    Kir2.2 (KCNJ12) (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12))

    Hintergrund

    KCNJ12 is an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). This gene is located within the Smith-Magenis syndrome region on chromosome 17.

    Molekulargewicht

    49 kDa
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