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OTX2 抗体

OTX2 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
产品编号 ABIN7269116
发货至: 中国
  • 抗原 See all OTX2 抗体
    OTX2 (Orthodenticle Homeobox 2 (OTX2))
    适用
    • 39
    • 29
    • 15
    • 5
    • 5
    • 5
    • 5
    • 5
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    • 4
    • 4
    • 4
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    • 1
    • 1
    • 1
    • 1
    宿主
    • 51
    • 4
    克隆类型
    • 51
    • 4
    单克隆
    标记
    • 28
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    • 1
    • 1
    • 1
    • 1
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    • 1
    • 1
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    This OTX2 antibody is un-conjugated
    应用范围
    • 39
    • 20
    • 13
    • 13
    • 13
    • 5
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    原理
    OTX2 Rabbit mAb
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Monoclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    A synthesized peptide derived from human OTX2
    亚型
    IgG
    Top Product
    Discover our top product OTX2 Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    OTX2 (Orthodenticle Homeobox 2 (OTX2))
    别名
    OTX2 (OTX2 产品)
    别名
    CPHD6 antibody, MCOPS5 antibody, E130306E05Rik antibody, id:ibd2915 antibody, zOtx2 antibody, zgc:136535 antibody, zotx-2 antibody, Xotx-2 antibody, Xotx2 antibody, otx-2 antibody, otx2 antibody, orthodenticle homeobox 2 antibody, orthodenticle homeobox 2 S homeolog antibody, orthodenticle homeobox 2 L homeolog antibody, OTX2 antibody, Otx2 antibody, otx2 antibody, otx2.S antibody, otx2.L antibody
    背景
    This gene encodes a member of the bicoid subfamily of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6). This gene is also suspected of having an oncogenic role in medulloblastoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Pseudogenes of this gene are known to exist on chromosomes two and nine. [provided by RefSeq, Jul 2012],CPHD6, MCOPS5,Cell Biology & Developmental Biology,Epigenetics & Nuclear Signaling,Neuroscience,Stem Cells,Transcription Factors,OTX2
    分子量
    32kDa
    基因ID
    5015
    UniProt
    P32243
    途径
    Dopaminergic Neurogenesis
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