EFHC1 抗体 (AbBy Fluor® 555)
Quick Overview for EFHC1 抗体 (AbBy Fluor® 555) (ABIN1400333)
抗原
See all EFHC1 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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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 EFHC1
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亚型
- IgG
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anti-EF-Hand Domain (C-terminal) Containing 1 (EFHC1) (AA 391-640) antibody
EFHC1 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-EF-Hand Domain (C-terminal) Containing 1 (EFHC1) (AA 1-640) antibodyEFHC1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-EF-Hand Domain (C-terminal) Containing 1 (EFHC1) (AA 270-378) antibodyEFHC1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4E7 unconjugated
anti-EF-Hand Domain (C-terminal) Containing 1 (EFHC1) (AA 1-640) antibodyEFHC1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-EF-Hand Domain (C-terminal) Containing 1 (EFHC1) (AA 32-81) antibodyEFHC1 适用: 人, 小鼠, 大鼠, Cow, 犬, 马 WB 宿主: 兔 Polyclonal unconjugated
anti-EF-Hand Domain (C-terminal) Containing 1 (EFHC1) (N-Term) antibodyEFHC1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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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 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- EFHC1 (EF-Hand Domain (C-terminal) Containing 1 (EFHC1))
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别名
- EFHC1
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背景
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Synonyms: EF hand domain C terminal containing 1, EF hand domain containing protein 1, EF-hand domain-containing protein 1, Efhc1, EFHC1_HUMAN, EJA1, EJM1, FLJ10466, FLJ37290, JAE, Myoclonin 1, Myoclonin-1.
Background: Defects in EFHC1 are the cause of juvenile myoclonic epilepsy type 1 (EJM1) [MIM:254770]. EJM1 is a subtype of idiopathic generalized epilepsy (IGE). Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.Genetic variations in EFHC1 are the cause of susceptibility to juvenile absence epilepsy type 1 (JAE1) . JAE is a subtype of idiopathic generalized epilepsy characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening, and myoclonic seizures.
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基因ID
- 114327
抗原
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