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

KCNJ12 Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN939681

Aperçu rapide pour Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12) Peptide (ABIN939681)

Antigène

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

Origine

Mammifères

Source

  • 2
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    KDLVENKFLL PSANSFCYEN ELAFLSRDEE DEADGDQDGR SRDGLSPQAR

    Attributs du produit

    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
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

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

    Sujet

    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.

    Poids moléculaire

    49 kDa
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