电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

PHD Finger Protein 6 (PHF6) (C-Term) Peptide

PHF6 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN981694
发货至: 中国
  • 抗原 See all PHF6 products
    PHF6 (PHD Finger Protein 6 (PHF6))
    蛋白结构域
    C-Term
    宿主
    资源
    • 5
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-PHF6 antibody (Catalog #: ARP51236_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    PHF6 (PHD Finger Protein 6 (PHF6))
    别名
    zgc:55403 Peptide, wu:fa22g03 Peptide, BFLS Peptide, BORJ Peptide, CENP-31 Peptide, 2700007B13Rik Peptide, 4931428F02Rik Peptide, mKIAA1823 Peptide, PHD finger protein 6 Peptide, PHD finger protein 6 L homeolog Peptide, phf6 Peptide, phf6.L Peptide, PHF6 Peptide, Phf6 Peptide
    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.

    Alias Symbols: BORJ, MGC14797, BFLS, CENP-31

    Protein Size: 312
    分子量
    35 kDa
    基因ID
    84295
    NCBI登录号
    NM_032335, NP_115711
    UniProt
    Q5JRC7
You are here:
客服