KV1.5 rabbit pAb

KV1.5 rabbit pAb

AO-06-ES2688-50

KV1.5 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES2688
Product nameKV1.5 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA;IHC
Other nameKCNA5; Potassium voltage-gated channel subfamily A member 5; HPCN1; Voltage-gated potassium channel HK2; Voltage-gated potassium channel subunit Kv1.5
Size50μL
Unit price ($)148
Human gene ID3741
Human Swiss-ProtP22460
SourceRabbit
IsotypeIgG
TargetKV1.5
Fields
Gene nameKCNA5
Protein namePotassium voltage-gated channel subfamily A member 5
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID16493
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ61762
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID25470
Rat gene linkView Rat Gene
Rat Swiss-ProtP19024
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human KCNA5. AA range:253-302
SpecificityKV1.5 Polyclonal Antibody detects endogenous levels of KV1.5 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)68kD
BackgroundPotassium 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
Functiondisease:Defects in KCNA5 are the cause of atrial fibrillation familial type 7 (ATFB7) [MIM:612240]. Atrial fibrillation is a common disorder of cardiac rhythm that is hereditary in a small subgroup of patients. It is characterized by disorganized atrial electrical activity, progressive deterioration of atrial electromechanical function and ineffective pumping of blood into the ventricles. It can be associated with palpitations, syncope, thromboembolic stroke, and congestive heart failure.,domain:The amino terminus may be important in determining the rate of inactivation of the channel while the C-terminal PDZ-binding motif may play a role in modulation of channel activity and/or targeting of the channel to specific subcellular compartments.,domain:The segment S4 is probably the voltage-sensor and is characterized by a series of positively charged amino acids at every third position.,func
Subcellular locationCell membrane ; Multi-pass membrane protein .
ExpressionPancreatic islets and insulinoma.

Additional Images

Image 1
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Western Blot analysis of various cells using KV1.5 Polyclonal Antibody diluted at 1:500
Image 2
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Western blot analysis of KCNA5 Antibody. The lane on the right is blocked with the KCNA5 peptide.
Image 3
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Western blot analysis of 293T with KV1.5 Rabbit pAb diluted at 1:2,000.
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Immunohistochemical analysis of paraffin-embedded human Gastric adenocarcinoma. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
: AO-06-ES2688-50
: 10 Produits
Hurry! only 10 items left in stock.

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