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RAX2 抗体

RAX2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7466343
发货至: 中国
  • 抗原 See all RAX2 抗体
    RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))
    适用
    • 6
    • 2
    • 1
    • 1
    宿主
    • 4
    • 2
    克隆类型
    • 6
    多克隆
    标记
    • 6
    This RAX2 antibody is un-conjugated
    应用范围
    • 6
    • 1
    Western Blotting (WB)
    交叉反应
    纯化方法
    Purified by antigen-affinity chromatography.
    免疫原
    Recombinant protein encompassing a sequence within the center region of human RAX2. The exact sequence is proprietary.
    亚型
    IgG
    Top Product
    Discover our top product RAX2 Primary Antibody
  • 应用备注
    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    说明

    Positive Control: IMR32

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.86 mg/mL
    缓冲液
    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
    储存液
    Thimerosal (Merthiolate)
    注意事项
    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原
    RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))
    别名
    retina and anterior neural fold homeobox 2 (RAX2 产品)
    别名
    qrx antibody, rx-l antibody, armd6 antibody, raxl1 antibody, cord11 antibody, ARMD6 antibody, CORD11 antibody, QRX antibody, RAXL1 antibody, retina and anterior neural fold homeobox 2 S homeolog antibody, retina and anterior neural fold homeobox 2 antibody, rax2.S antibody, RAX2 antibody
    背景
    Retina and anterior neural fold homeobox 2 , ARMD6 , CORD11 , QRX , RAXL1,This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. [provided by RefSeq]
    分子量
    20 kDa
    基因ID
    84839
    UniProt
    Q96IS3
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