KCNJ2 Polyclonal Antibody (E-AB-52110)

For research use only.
Verified Samples |
Verified Samples in IHC: Human liver cancer |
Dilution | IHC 1:30-1:150 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Synthetic peptide of human KCNJ2 |
Abbre | KCNJ2 |
Synonyms | Cardiac inward rectifier potassium channel, HHBIRK 1, HHBIRK1, HHIRK 1, HHIRK1, HIRK 1, IRK 1, IRK-1, IRK1, IRK2, Inward rectifier K, Inward rectifier K(+) channel Kir2.1, Inward rectifier potassium channel 2, KCNJ2, KIR2., hIRK1, inwardly rectifying subfamily J member 2 |
Swissprot | |
Cellular Localization | Membrane. |
Concentration | 0.96 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Antigen affinity purification |
Research Areas | Cancer, Neuroscience |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. |
Other Clones
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Other Formats
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Unconjugated
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