A9935
KCNJ6 Rabbit polyclonal antibody

Size
£151.00
- SKU:
- A9935
- Additional Names:
- BIR1|GIRK-2|GIRK2|hiGIRK2|KATP-2|KATP2|KCNJ6|KCNJ7|KIR3.2|KPLBS
- Application:
- ELISA, WB
- Molecular Weight:
- 48kDa
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Abclonal
- Host:
- Rabbit
- Reactivities:
- Human, Mouse
- Immunogen:
- Recombinant protein (or fragment).This information is considered to be commercially sensitive.
- Formulation:
- Unmodified
- Sequence:
- MAKLTESMTNVLEGDSMDQDVESPVAIHQPKLPKQARDDLPRHISRDRTKRKIQRYVRKDGKCNVHHGNVRETYRYLTDI
- Uniprot:
- P48051
- Synonyms:
- BIR1;G protein-activated inward rectifier potassium channel 2;GIRK-2;GIRK2;hiGIRK2;inward rectifier K(+) channel Kir3.2;inward rectifier potassium channel KIR3.2;KATP-2;KATP2;KCNJ7;KIR3.2;KPLBS;Potassium channel, inwardly rectifying subfamily J member 6;potassium channel, inwardly rectifying subfamily J, member 6;potassium voltage-gated channel subfamily J member 6
- Extra Details:
- This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.
- Shipping Conditions:
- Blue Ice

