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Anticorps Polyclonal de lapin anti-KCNQ3

KCNQ3 Polyclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 24580-1-PBS

Synonymes

Galerie de données de validation

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  • Western Blot (WB) analysis of various lysates using KCNQ3 Polyclonal antibody (24580-1-AP)

    WB analysis using 24580-1-AP (same clone as 24580-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 24580-1-AP (KCNQ3 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 24580-1-PBS in a different storage buffer formulation.

Informations sur le produit

24580-1-PBS cible KCNQ3 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Hôte / Isotype Lapin / IgG
Clonalité Polyclonal
Type Anticorps
Immunogène KCNQ3 Protéine recombinante Ag20147
Nom complet potassium voltage-gated channel, KQT-like subfamily, member 3
Masse moléculaire calculée 872 aa, 97 kDa
Poids moléculaire observé~90 kDa
Numéro d’acquisition GenBankBC128576
Symbole du gène KCNQ3
Identification du gène (NCBI) 3786
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par affinité contre l'antigène
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

KCNQ3, also named as BFNC2, EBN2 and KV7.3, belongs to the potassium channel family and KQT subfamily. KCNQ3 is probably important in the regulation of neuronal excitability. Associates with KCNQ2 or KCNQ5, KCNQ3 forms a potassium channel with essentially identical properties to the channel underlying the native M-current, a slowly activating and deactivating potassium conductance which plays a critical role in determining the subthreshold electrical excitability of neurons as well as the responsiveness to synaptic inputs. Defects in KCNQ3 are the cause of benign neonatal epilepsy type 2 (EBN2).

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