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EFHC1 抗体 (Alexa Fluor 594)

EFHC1 适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal Alexa Fluor 594
产品编号 ABIN2812685
发货至: 中国
  • 抗原 See all EFHC1 抗体
    EFHC1 (EF-Hand Domain (C-terminal) Containing 1 (EFHC1))
    适用
    • 28
    • 20
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 24
    • 4
    克隆类型
    • 26
    • 2
    多克隆
    标记
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This EFHC1 antibody is conjugated to Alexa Fluor 594
    应用范围
    • 26
    • 12
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human EFHC1
    亚型
    IgG
    Top Product
    Discover our top product EFHC1 Primary Antibody
  • 应用备注
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    EFHC1 (EF-Hand Domain (C-terminal) Containing 1 (EFHC1))
    别名
    EFHC1 (EFHC1 产品)
    别名
    MGC63931 antibody, zgc:63931 antibody, MGC84469 antibody, MGC89313 antibody, dJ304B14.2 antibody, 1700029F22Rik antibody, mRib72-1 antibody, myoclonin1 antibody, EF-hand domain containing 1 antibody, EF-hand domain (C-terminal) containing 1 antibody, EF-hand domain (C-terminal) containing 1 L homeolog antibody, Efhc1 antibody, EFHC1 antibody, efhc1 antibody, efhc1.L antibody
    背景

    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.

    基因ID
    114327
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