KCTD7 抗体 (AA 112-180)
Quick Overview for KCTD7 抗体 (AA 112-180) (ABIN1387694)
抗原
See all KCTD7 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 112-180
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交叉反应
- 人
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预测反应
- Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human KCTD7
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亚型
- IgG
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anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) antibody
KCTD7 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (N-Term) antibodyKCTD7 适用: 人, 小鼠, 大鼠, Cow, 犬, 马, Pig, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (AA 1-289) antibodyKCTD7 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (AA 181-230) antibodyKCTD7 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (AA 5-152) antibodyKCTD7 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (N-Term) antibodyKCTD7 适用: 人, 小鼠, 大鼠, Cow, 犬, 马, Pig, 兔, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (N-Term) antibodyKCTD7 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
ELISA 1:500-1000
FCM 1:20-100
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))
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别名
- KCTD7
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背景
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Synonyms: BTB/POZ domain containing protein KCTD7, EPM3, FLJ32069, Potassium channel tetramerisation domain containing 7, KCTD7_HUMAN.
Background: Epilepsy affects about 0.5 % of the world?s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
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基因ID
- 154881
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UniProt
- Q96MP8
抗原
-
