GTX644460
Kv1.5 antibody [GT241]
Cannot supply to this region.
- SKU:
- GTX644460
- Additional Names:
- potassium voltage-gated channel subfamily A member 5 , ATFB7 , HCK1 , HK2 , HPCN1 , KV1.5 , PCN1
- Application:
- WB
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human, Mouse
- Purification:
- Protein A Purified
- Storage Conditions:
- -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.
- Supplier:
- Genetex
- Host:
- Mouse
- Reactivities:
- Mouse, Rat
- Buffer:
- PBS, no preservatives.
- Immunogen:
- The immunogen used to generate this antibody corresponds to human Kv1.5.
- Clone:
- GT241
- Uniprot:
- P22460
- Synonyms:
- ATFB7;cardiac potassium channel;HCK1;HK2;HPCN1;insulinoma and islet potassium channel;KV1.5;PCN1;potassium channel 1;potassium channel, voltage gated shaker related subfamily A, member 5;potassium voltage-gated channel subfamily A member 5;potassium voltage-gated channel, shaker-related subfamily, member 5;voltage-gated potassium channel HK2;voltage-gated potassium channel protein Kv1.5;voltage-gated potassium channel subunit Kv1.5
- Extra Details:
- Potassium channels represent the most complex class of voltage-gated ino 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. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, the function of which could restore the resting membrane potential of beta cells after depolarization and thereby contribute to the regulation of insulin secretion. This gene is intronless, and the gene is clustered with genes KCNA1 and KCNA6 on chromosome 12. Defects in this gene are a cause of familial atrial fibrillation type 7 (ATFB7). [provided by RefSeq, May 2012]
- Shipping Conditions:
- Blue Ice