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  2. Polyclonal

GTX54296

KCNE1 antibody

Cannot supply to this region.

SKU:
GTX54296
Additional Names:
potassium voltage-gated channel subfamily E regulatory subunit 1 , ISK , JLNS , JLNS2 , LQT2/5 , LQT5 , MinK
Application:
WB
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity 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:
Rabbit
Reactivities:
Human, Mouse
Buffer:
PBS, 50% Glycerol, 0.02% Sodium azide.
Immunogen:
A synthetic peptide corresponding to a sequence within amino acids 1-100 of human KCNE1 (NP_000210.2).
Uniprot:
P15382
Synonyms:
cardiac delayed rectifier potassium channel protein;delayed rectifier potassium channel subunit IsK;IKs producing slow voltage-gated potassium channel subunit beta Mink;ISK;JLNS;JLNS2;Long QT syndrome 5;LQT2/5;LQT5;minimal potassium channel;MinK;potassium channel, voltage gated subfamily E regulatory beta subunit 1;potassium voltage-gated channel subfamily E member 1;potassium voltage-gated channel, Isk-related family, member 1;potassium voltage-gated channel, Isk-related subfamily, member 1;voltage gated potassiun channel accessory subunit
Extra Details:
The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Shipping Conditions:
Blue Ice