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- 抗原 See all KCNQ1 抗体
- KCNQ1 (Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This KCNQ1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human KCNQ1
- 亚型
- IgG
- Top Product
- Discover our top product KCNQ1 Primary Antibody
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anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody
KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) unconjugated
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (HRP)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) HRP
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (FITC)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) FITC
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (Biotin)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) Biotin
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (PE)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) PE
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (APC)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) APC
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (PerCP)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) PerCP
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (Atto 488)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) Atto 488
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (Atto 594)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) Atto 594
anti-Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1) (AA 2-101) antibody (Atto 390)KCNQ1 适用: 人 WB, IHC, IP, ICC, IF, AA 宿主: 小鼠 Monoclonal N37A-10 (Formerly S37A-10) Atto 390
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- 应用备注
- WB 1:200-1:1000, IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.2 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 储存液
- Sodium azide
- 注意事项
- Avoid freeze / thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- KCNQ1 (Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 (KCNQ1))
- 别名
- KCNQ1 (KCNQ1 产品)
- 别名
- ATFB1 antibody, ATFB3 antibody, JLNS1 antibody, KCNA8 antibody, KCNA9 antibody, KVLQT1 antibody, Kv1.9 antibody, Kv7.1 antibody, LQT antibody, LQT1 antibody, RWS antibody, SQT2 antibody, WRS antibody, CG12215 antibody, CG12915 antibody, CG33135 antibody, DKCNQ antibody, Dmel\\CG33135 antibody, dKCNQ antibody, kcnq1 antibody, KCNQ1 antibody, kqt-3 antibody, kv7.1 antibody, Kvlqt1 antibody, KvLQT-1 antibody, kcnq1-A antibody, xkvlqt1 antibody, zgc:158384 antibody, AW559127 antibody, Kcna9 antibody, KvLQT1 antibody, potassium voltage-gated channel subfamily Q member 1 antibody, KCNQ potassium channel antibody, potassium voltage-gated channel, KQT-like subfamily, member 1 antibody, potassium channel, voltage gated KQT-like subfamily Q, member 1 antibody, voltage gated potassium channel subunit antibody, potassium channel, voltage gated KQT-like subfamily Q, member 1 L homeolog antibody, potassium voltage-gated channel, subfamily Q, member 1 antibody, KCNQ1 antibody, KCNQ antibody, kcnq1 antibody, Kcnq1 antibody, kcnq1.L antibody
- 背景
- 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.
- 分子量
- Calculated MW: 75 kDa
- NCBI登录号
- NP_000209
- 途径
- Negative Regulation of Hormone Secretion, Sensory Perception of Sound
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