KCNJ10 Antibody

Product Specifications

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.

NCBI Gene ID

3766

Swiss Prot

P78508

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

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

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Neuroscience

Purification

Affinity purification

Positive Control

293T

Concentration

Batch dependent

Buffer

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

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

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

Calculated Molecular Weight

Observed: 42kDa

Fragment

IgG

Applications Notes

WB: 1:500 - 1:2000

Symbol

KCNJ10

Positive Control 2

MCF7

Positive Control 3

Mouse brain

Positive Control 4

Rat brain

NCBI Official Name

Potassium voltage-gated channel subfamily J member 10

NCBI Organism

Homo sapiens

Other Product Names

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