KIR2.1 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES2675
Catalog Number: ELK-ES2675
Reactivity: Human, Rat
Applications: WB, IHC-p, ELISA
Information
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Reactivity: Human, Rat
Applications: WB, IHC-p, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
potassium voltage-gated channel subfamily J member 2(KCNJ2) Homo sapiens 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. [provided by RefSeq, Jul 2008],
Alternative Names:
KCNJ2, IRK1, Inward rectifier potassium channel 2, Cardiac inward rectifier potassium channel, Inward rectifier K(+) channel Kir2.1, IRK-1, hIRK1, Potassium channel, inwardly rectifying subfamily J m
Immunogen: The antiserum was produced against synthesized peptide derived from human KCNJ2. AA range:81-130
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 48
GeneID: KCNJ2
Storage: -20°C/1 year
NOTE: For Research Use Only
potassium voltage-gated channel subfamily J member 2(KCNJ2) Homo sapiens 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. [provided by RefSeq, Jul 2008],
Alternative Names:
KCNJ2, IRK1, Inward rectifier potassium channel 2, Cardiac inward rectifier potassium channel, Inward rectifier K(+) channel Kir2.1, IRK-1, hIRK1, Potassium channel, inwardly rectifying subfamily J m
Immunogen: The antiserum was produced against synthesized peptide derived from human KCNJ2. AA range:81-130
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 48
GeneID: KCNJ2
Storage: -20°C/1 year
NOTE: For Research Use Only
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