电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

ZNF141 抗体

ZNF141 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2458313
发货至: 中国
  • 抗原 See all ZNF141 抗体
    ZNF141 (Zinc Finger Protein 141 (ZNF141))
    适用
    • 8
    • 2
    • 1
    • 1
    • 1
    宿主
    • 8
    克隆类型
    • 8
    多克隆
    标记
    • 8
    This ZNF141 antibody is un-conjugated
    应用范围
    • 6
    • 2
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ZNF141.
    Top Product
    Discover our top product ZNF141 Primary Antibody
  • 应用备注
    ZNF141 antibody can be used for detection of ZNF141 by ELISA at 1:312500. ZNF141 antibody can be used for detection of ZNF141 by western blot at 1 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 50 ?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 ZNF141 antibody at -20 °C.
  • 抗原
    ZNF141 (Zinc Finger Protein 141 (ZNF141))
    别名
    ZNF141 (ZNF141 产品)
    背景
    Zinc finger encoding genes would be good candidates for being involved in the multiple developmental defects associated with chromosomal aneusomy--because of their role as transcriptional regulators, their abundance in the genome and their known association with specific developmental disorders. A zinc finger encoding cDNA (ZNF141) of the C2-H2/KRAB subfamily has been mapped to the 4p- (Wolf-Hirschhorn) syndrome (WHS) chromosome region. ZNF141 was expressed ubiquitously at low levels in the analysed tissue. The identification of a candidate gene for a chromosomal aneusomy syndrome belonging to a class of evolutionary conserved genes will provide options for studying its normal and abnormal expression during mammalian embryogenesis.
    分子量
    55 kDa
    基因ID
    7700
    NCBI登录号
    NP_003432
    UniProt
    Q15928
You are here:
客服