anti-KCNQ1 antibody

Key features and details

  • 产品描述: Goat Polyclonal antibody recognizes KCNQ1
  • 反应物种: Hu
  • 预测物种: Ms, Rat, Cow, Dog
  • 应用: WB
  • 特异性: This antibody is expected to recognize both reported isoforms (NP_000209.2; NP_861463.1).
  • 宿主: Goat
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: KCNQ1
  • Brand:
CAT.NO. : ARG64865
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Product Details
概述
产品描述Goat Polyclonal antibody recognizes KCNQ1
反应物种Hu
预测物种Ms, Rat, Cow, Dog
应用WB
特异性This antibody is expected to recognize both reported isoforms (NP_000209.2; NP_861463.1).
宿主Goat
克隆Polyclonal
同位型IgG
靶点名称KCNQ1
抗原物种Human
抗原C-EQLTVPRRGPDEGS
偶联标记Un-conjugated
別名Voltage-gated potassium channel subunit Kv7.1; KQT-like 1; JLNS1; LQT; KVLQT1; Kv1.9; KCNA9; IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1; SQT2; RWS; LQT1; WRS; KCNA8; ATFB3; Potassium voltage-gated channel subfamily KQT member 1; Kv7.1; ATFB1
应用说明
应用建议
应用推荐稀释比
WB1 - 3 µg/ml
应用说明WB: Recommend incubate at RT for 1h.
* 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Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
缓冲液Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
抗菌剂0.02% Sodium azide
稳定剂0.5% BSA
浓度0.5 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 or below. 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: 3784 Human KCNQ1

Swiss-port # P51787 Human Potassium voltage-gated channel subfamily KQT member 1

背景介绍This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]
研究领域Cell Biology and Cellular Response antibody; Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody
预测分子量75 kDa
翻译后修饰Phosphorylation at Ser-27 by PKA; increases delayed rectifier potassium channel activity of the KCNQ1-KCNE1 complex through a macromolecular complex that includes PKA, PP1, and the targeting protein AKAP9.
Ubiquitinated by NEDD4L; promotes internalization (PubMed:22024150). The ubiquitinylated form is internalized through a clathrin-mediated endocytosis by interacting with AP2M1 and is recycled back to the cell membrane via RAB4A and RAB11A (PubMed:23529131).
Deubiquitinated by USP2; counteracts the NEDD4L-specific down-regulation of I(Ks) and restores the membrane localization.
检测图片 (1)
  • ARG64865 anti-KCNQ1 antibody WB image

    Western Blot: Human Heart lysate (35 µg protein in RIPA buffer) stained with ARG64865 anti-KCNQ1 antibody at 1 µg/ml dilution.

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