KCTD7 抗体
Quick Overview for KCTD7 抗体 (ABIN7245461)
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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产品特性
- Polyclonal Antibody
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纯化方法
- Antigen affinity purification
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免疫原
- Synthetic peptide of human KCTD7
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亚型
- IgG
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anti-Potassium Channel Tetramerisation Domain Containing 7 (KCTD7) (N-Term) antibody
KCTD7 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
- WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1.56 mg/mL
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缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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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
- KCTD7 (Potassium Channel Tetramerization Domain Containing 7) is a Protein Coding gene. Diseases associated with KCTD7 include Epilepsy, Progressive Myoclonic 3, With Or Without Intracellular Inclusions and Cln14 Disease. Among its related pathways are Neuropathic Pain-Signaling in Dorsal Horn Neurons and Innate Immune System. An important paralog of this gene is KCTD14. This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.
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分子量
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Observed_MW: Refer to figures
Calculated_MW: 33 kDa
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UniProt
- Q96MP8
抗原
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