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CRX 抗体

This anti-CRX antibody is a 兔 多克隆 antibody detecting CRX in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN7467413
发货至: 中国

Quick Overview for CRX 抗体 (ABIN7467413)

抗原

See all CRX 抗体
CRX (Cone-Rod Homeobox (CRX))

适用

  • 24
  • 23
  • 23

宿主

  • 32
  • 4
  • 1
  • 1

克隆类型

  • 34
  • 4
多克隆

标记

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  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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This CRX antibody is un-conjugated

应用范围

  • 15
  • 13
  • 13
  • 11
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    人, 小鼠

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human CORD2. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: SK-N-SH , APRE19 , mouse eye

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS ( pH 7), 1 % BSA, 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

    CRX (Cone-Rod Homeobox (CRX))

    别名

    cone-rod homeobox

    背景

    Cone-rod homeobox , CORD2 , CRD , LCA7 , OTX3,The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined. [provided by RefSeq]

    分子量

    32 kDa

    基因ID

    1406

    UniProt

    O43186
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