ZBTB14 | ZFP161 Rabbit pAb, PerCP-Cy7 conj.(bs-18527R-PerCP-Cy7)-100ul产品图

ZBTB14 | ZFP161 Rabbit pAb, Pe

rCP-Cy7 conj.(bs-18527R-PerCP-Cy7)-100ul
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  • ¥2980
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  • bs-18527R-PerCP-Cy7
  • 2026年10月17日
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    • 技术资料
    • 规格:

      100ul

    产品编号bs-18527R-PerCP-Cy7
    英文名称ZFP161 Rabbit pAb, PerCP-Cy7 conjugated
    中文名称PerCP-Cy7标记的锌指蛋白161抗体
    英文别名HZF5; MGC126126; ZBTB14; ZF161_HUMAN; ZF5; Zfp 161; Zfp-161; Zfp-5; Zfp161; Zinc finger and BTB domain containing protein 14; Zinc finger and BTB domain-containing protein 14; Zinc finger protein 161 homolog(mouse); Zinc finger protein 161 homolog; Zinc finger protein 478; Zinc finger protein 5; Zinc finger protein 5 homolog; Zinc finger protein homologous to Zfp161 in mouse; ZNF478.
    产品应用IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human ZFP161
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    亚细胞定位Nucleus.
    相似性Belongs to the krueppel C2H2-type zinc-finger protein family.
    _x000D_ Contains 1 BTB (POZ) domain.
    _x000D_ Contains 5 C2H2-type zinc fingers.
    功能Transcriptional repressor of MYC and thymidine kinase promoters (By similarity). Transcriptional activator of the dopamine transporter (DAT), binding it's promoter at the consensus sequence 5'-CCTGCACAGTTCACGGA-3'.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料ZFP161 is a 449 amino acid member of the Krüppel C2H2-type zinc-finger protein family. Localized to distinct regions within the nucleus, ZFP161 functions both as a transcriptional repressor of Thymidine Kinase (TK) and c-Myc promoters and as a transcriptional activator of the dopamine transporter (DAT) promoter. ZFP161 contains one BTB (POZ) domain and five C2H2-type zinc fingers which direct its specific localization and nucleic acid binding, respectively. Defects in the gene encoding ZFP161 may be associated with holoprosencephaly type 4 (HPE4), a structural anomaly of the brain characterized by a flattened nasal tip with no visible septum, hypotelorism, lack of nasal bridge, ptosis of the left upper eyelid and, in some cases, infant death.

     

    应用推荐稀释比例
    {IF}{1:100-500}

     

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