ARG24120

anti-KCNQ4 antibody [N43/6]

anti-KCNQ4 antibody [N43/6] for ICC/IF,IHC-Frozen sections,IHC-Formalin-fixed paraffin-embedded sections,Immunoprecipitation,Western blot and Human,Mouse,Rat

Neuroscience antibody

概述

产品描述 Mouse Monoclonal antibody [N43/6] recognizes KCNQ4
反应物种 Hu, Ms, Rat
应用 ICC/IF, IHC-Fr, IHC-P, IP, WB
宿主 Mouse
克隆 Monoclonal
克隆号 N43/6
同位型 IgG1
靶点名称 KCNQ4
抗原物种 Human
抗原 Fusion protein of human KCNQ4 (a.a 2-77 )
偶联标记 Un-conjugated
別名 DFNA2; Voltage-gated potassium channel subunit Kv7.4; KQT-like 4; DFNA2A; Potassium voltage-gated channel subfamily KQT member 4; KV7.4; Potassium channel subunit alpha KvLQT4

应用说明

应用建议
应用 推荐稀释比
ICC/IF1:100
IHC-Fr1:1000
IHC-P1:1000
IPAssay-dependent
WB1:1000
应用说明 * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

属性

形式 Liquid
纯化 Purification with Protein G.
缓冲液 PBS (pH 7.4), 50% Glycerol and 0.09% Sodium azide
抗菌剂 0.09% Sodium azide
稳定剂 50% Glycerol
浓度 1 mg/ml
存放说明 For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项 For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接

GeneID: 60613 Mouse KCNQ4

GeneID: 9132 Human KCNQ4

Swiss-port # P56696 Human Potassium voltage-gated channel subfamily KQT member 4

Swiss-port # Q9JK97 Mouse Potassium voltage-gated channel subfamily KQT member 4

基因名称 KCNQ4
全名 Potassium Voltage-Gated Channel Subfamily Q Member 4
背景介绍 The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
研究领域 Neuroscience antibody
预测分子量 77 kDa

检测图片 (4) Click the Picture to Zoom In

  • ARG24120 anti-KCNQ4 antibody [N43/6] IHC-P image

    Immunohistochemistry: Human hippocampus stained with ARG24120 anti-KCNQ4 antibody [N43/6] at 1:1000 dilution.

  • ARG24120 anti-KCNQ4 antibody [N43/6] ICC/IF image

    Immunofluorescence: SH-SY5Y stained with ARG24120 anti-KCNQ4 antibody [N43/6] at 1:100 dilution.

  • ARG24120 anti-KCNQ4 antibody [N43/6] WB image

    Western blot: Rat tissue lysate stained with ARG24120 anti-KCNQ4 antibody [N43/6] at 1:200 dilution.

  • ARG24120 anti-KCNQ4 antibody [N43/6] IHC-Fr image

    Immunohistochemistry: Mouse Brain stained with ARG24120 anti-KCNQ4 antibody [N43/6] at 1:1000 dilution.