KCNJ10 Antibody | 23-926

KCNJ10 Antibody | 23-926 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human, Mouse, Rat

Homology: N/A

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 50-150 of human KCNJ10 (NP_002232.2) .

Research Area: Neuroscience

Tested Application: WB

Application: WB: 1:500 - 1:2000

Specificiy: N/A

Positive Control 1: 293T

Positive Control 2: MCF7

Positive Control 3: Mouse brain

Positive Control 4: Rat brain

Positive Control 5: N/A

Positive Control 6: N/A

Molecular Weight: Observed: 42kDa

Validation: N/A

Isoform: N/A

Purification: Affinity purification

Clonality: Polyclonal

Clone: N/A

Isotype: IgG

Conjugate: Unconjugated

Physical State: Liquid

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Concentration: N/A

Storage Condition: Store at -20˚C. Avoid freeze / thaw cycles.

Alternate Name: BIRK-1KCNJ13-PEN, KIR1.2, KIR4.1, SESAME, ATP-sensitive inward rectifier potassium channel 1ATP-dependent inwardly rectifying potassium channel Kir4.1, glial ATP-dependent inwardly rectifying potassium channel KIR4.1, inward rectifier K (+) channel Kir1.2, inward rectifier K+ channel KIR1.2, potassium channel, inwardly rectifying subfamily J member 1potassium inwardly-rectifying channel, subfamily J, member 10

User Note: Optimal dilutions for each application to be determined by the researcher.

BACKGROUND: This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes.