GTX88962-PEP
GIRK2 blocking peptide
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX88962-PEP
- Zusätzliche Namen:
- Potassium Voltage-Gated Channel Subfamily J Member 6 , Bir1 , Girk-2 , Girk2 , Katp-2 , Katp2 , Kcnj7 , Kir3.2 , Kplbs , Higirk2 , Kcnj6
- Physischer Zustand:
- Lyophilized
- Lagerbedingungen:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Hersteller:
- Genetex
- Buffer:
- Reconstitute with 200ul distilled water to obtain a 0.5mg/ml peptide solution. Lyophilized from 5% (v/v) acetonitrile/H₂O, no preservatives.
- Immunogen:
- potassium voltage-gated channel subfamily J member 6
- Spezies:
- Human
- Synonyme:
- 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 voltage-gated channel subfamily J member 6
- Weitere 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. [provided by RefSeq, Apr 2015]
- Versandbedingungen:
- Blue Ice