GTX87812
KCNT1 antibody
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX87812
- Zusätzliche Namen:
- EIEE14 , ENFL5 , KCNT1 , KCa4.1 , SLACK , Slo2.2 , bA100C15.2 , potassium sodiumactivated channel subfamily T member 1 , potassium sodium-activated channel subfamily T member 1
- Anwendung:
- IHC-P
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified
- 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
- Host:
- Rabbit
- Reaktivitäten:
- Human
- Buffer:
- PBS, 150mM NaCl, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- The antiserum was produced against synthesized peptide derived from human KCNT1 (1019-1068).
- Uniprot:
- Q5JUK3
- Synonyme:
- bA100C15.2;DEE14;EIEE14;ENFL5;KCa4.1;potassium channel subfamily T member 1;potassium channel, sodium activated subfamily T, member 1;potassium channel, subfamily T, member 1;Sequence like a calcium-activated K+ channel;SLACK;Slo2.2
- Weitere Details:
- Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
- Versandbedingungen:
- Blue Ice