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ZBTB20 抗体

ZBTB20 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7012097
发货至: 中国
  • 抗原 See all ZBTB20 抗体
    ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))
    适用
    • 12
    • 6
    • 5
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 12
    • 1
    克隆类型
    • 12
    • 1
    多克隆
    标记
    • 13
    This ZBTB20 antibody is un-conjugated
    应用范围
    • 10
    • 5
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human ZBTB20 (NP_056457.3).
    亚型
    IgG
    Top Product
    Discover our top product ZBTB20 Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))
    别名
    ZBTB20 (ZBTB20 产品)
    别名
    DPZF antibody, HOF antibody, ODA-8S antibody, ZNF288 antibody, 1300017A20Rik antibody, 7330412A13Rik antibody, A930017C21Rik antibody, D16Wsu73e antibody, Oda8 antibody, Zfp288 antibody, RGD1560387 antibody, zinc finger and BTB domain containing 20 antibody, ZBTB20 antibody, Zbtb20 antibody
    背景
    This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    分子量

    Observed_MW: 81 kDa

    Calculated_MW: 73 kDa/81 kDa

    基因ID
    26137
    UniProt
    Q9HC78
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