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KDM5C 抗体 (full length)

The 小鼠 单克隆 anti-KDM5C antibody (Clone PCRP-KDM5C-1A11) (ABIN7878544) specifically detects KDM5C in FACS. The antibody is reactive with 人 samples.
产品编号 ABIN7878544
发货至: 中国
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Quick Overview for KDM5C 抗体 (full length) (ABIN7878544)

抗原

See all KDM5C 抗体
KDM5C (Lysine (K)-Specific Demethylase 5C (KDM5C))

适用

  • 37
  • 6
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  • 4
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  • 1
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宿主

  • 25
  • 12
小鼠

克隆类型

  • 25
  • 12
单克隆

标记

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  • 2
  • 1
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  • 1
  • 1
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  • 1
This KDM5C antibody is un-conjugated

应用范围

  • 20
  • 13
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  • 1
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Flow Cytometry (FACS)

质量等级

Carrier-free

克隆位点

PCRP-KDM5C-1A11
  • 抗原表位

    • 7
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    full length

    原理

    JARID1C Antibody / KDM5C / SMCX (azide and preservative free)

    纯化方法

    Protein A/G affinity

    免疫原

    Recombinant full-length human protein was used as the immunogen for the JARID1C antibody.

    亚型

    IgG2c
  • 应用备注

    Optimal dilution of the JARID1C antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C

    储存方法

    Aliquot the JARID1C antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    KDM5C (Lysine (K)-Specific Demethylase 5C (KDM5C))

    别名

    JARID1C

    背景

    SmcX, also known as JARID1C (jumonji, AT rich interactive domain 1C), MRXJ, KDM5C or XE169, is a nuclear protein that contains one ARID domain, one JmjC domain, one JmjN domain and two PHD-type zinc fingers and belongs to the JARID1 histone demethylase family. Expressed ubiquitously with highest expression in brain and skeletal muscle, SmcX functions as a histone demethylase that removes methyl groups from lysine residues on Histone H3, thereby playing a role in the histone code, as well as transcriptional regulation and chromatin remodeling. SmcX binds iron and a-ketoglutarate as cofactors and can recruit histone deacetylases to neuron silencer elements, thus repressing the transcription of neuronal genes. Defects in the gene encoding SmcX are associated with X-linked mental retardation (XLMR), a condition characterized by cognitive impairment and a low IQ. Multiple isoforms of SmcX are expressed due to alternative splicing events.

    UniProt

    P41229

    途径

    Warburg Effect
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