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

OVOL2 抗体

OVOL2 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7246562
发货至: 中国
  • 抗原 See all OVOL2 抗体
    OVOL2 (Ovo-Like 2 (OVOL2))
    适用
    • 28
    • 24
    • 19
    • 4
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 37
    • 3
    克隆类型
    • 39
    • 1
    多克隆
    标记
    • 16
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This OVOL2 antibody is un-conjugated
    应用范围
    • 28
    • 13
    • 13
    • 9
    • 7
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Fusion protein of human OVOL2
    亚型
    IgG
    Top Product
    Discover our top product OVOL2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.84 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    OVOL2 (Ovo-Like 2 (OVOL2))
    别名
    OVOL2 (OVOL2 产品)
    别名
    znf339 antibody, MGC89597 antibody, EUROIMAGE566589 antibody, ZNF339 antibody, 1700108N11Rik antibody, 1810007D21Rik antibody, M-OVO antibody, M-OVO-A antibody, M-OVO-B antibody, MOVO antibody, Ovo2 antibody, Zfp339 antibody, movo2 antibody, ovo like zinc finger 2 antibody, ovo-like zinc finger 2 antibody, OVOL2 antibody, ovol2 antibody, Ovol2 antibody
    背景
    This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 30 kDa

    UniProt
    Q9BRP0
    途径
    Tube Formation
You are here:
客服