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PHF6 抗体

This anti-PHF6 antibody is a 兔 多克隆 antibody detecting PHF6 in WB 和 ELISA. Suitable for 人 和 犬.
产品编号 ABIN2463418
发货至: 中国

Quick Overview for PHF6 抗体 (ABIN2463418)

抗原

See all PHF6 抗体
PHF6 (PHD Finger Protein 6 (PHF6))

适用

  • 36
  • 9
  • 7
  • 7
  • 7
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 1
人, 犬

宿主

  • 34
  • 2

克隆类型

  • 35
  • 1
多克隆

标记

  • 26
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PHF6 antibody is un-conjugated

应用范围

  • 24
  • 9
  • 7
  • 7
  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by protein A chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PHF6.
  • 应用备注

    PHF6 antibody can be used for detection of PHF6 by ELISA at 1:312500. PHF6 antibody can be used for detection of PHF6 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store PHF6 antibody at -20 °C.
  • 抗原

    PHF6 (PHD Finger Protein 6 (PHF6))

    别名

    PHF6

    背景

    PHF6 is a member of the plant homeodomain (PHD)-like finger (PHF) family. PHF6 is a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of its gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS).This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

    分子量

    35 kDa, 41 kDa, 41 kDa

    基因ID

    84295

    NCBI登录号

    NP_115711

    UniProt

    Q8IWS0
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