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CDKL5 抗体 (C-Term)

This anti-CDKL5 antibody is a 兔 多克隆 antibody detecting CDKL5 in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN391362
发货至: 中国

Quick Overview for CDKL5 抗体 (C-Term) (ABIN391362)

抗原

See all CDKL5 抗体
CDKL5 (Cyclin-Dependent Kinase-Like 5 (CDKL5))

适用

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宿主

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克隆类型

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多克隆

标记

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This CDKL5 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

RB3556
  • 抗原表位

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    AA 982-1012, C-Term

    纯化方法

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    免疫原

    This CDKL5 (STK9) antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 982-1012 amino acids from the C-terminal region of human CDKL5 (STK9).

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000. IHC-P: 1:10~50

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    CDKL5 (Cyclin-Dependent Kinase-Like 5 (CDKL5))

    别名

    CDKL5 (STK9)

    背景

    Defects in STK9, a dual-specificity serine/threonine kinase, are a cause of atypical Rett syndrome. Rett syndrome is an X-linked dominant disease. It is a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. Patients appear to develop normally until 6 to 18 months of age, then gradually lose speech and purposeful hand movements and develop microcephaly, seizures, autism, ataxia, intermittent hyperventilation, and stereotypic hand movements. After initial regression, the condition stabilizes and patients usually survive into adulthood. Rett syndrome due to CDKL5-associated mutations is characterized by a severe early-onset phenotype and atypical features such as infantile spasms.

    分子量

    107519

    基因ID

    6792

    NCBI登录号

    NP_001032420, NP_003150

    UniProt

    O76039

    途径

    Regulation of Cell Size
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