anti-KCNQ4 antibody [N43/6]

CAT.NO. : ARG24120

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Size:

50 μg

*产品价格可能会有所调整，请以品牌方官网实时更新的价格为准，以确保准确性。

Product Details

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)

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.

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