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CRX 抗体 (AA 265-299)

CRX 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5647525
发货至: 中国
  • 抗原 See all CRX 抗体
    CRX (Cone-Rod Homeobox (CRX))
    抗原表位
    • 15
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 265-299
    适用
    • 24
    • 23
    • 22
    宿主
    • 31
    • 4
    • 1
    • 1
    克隆类型
    • 34
    • 3
    多克隆
    标记
    • 16
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CRX antibody is un-conjugated
    应用范围
    • 14
    • 13
    • 13
    • 11
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Antigen affinity purified
    免疫原
    Amino acids 265-299 (DSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL) from the human protein were used as the immunogen for the CRX antibody.
    亚型
    IgG
    Top Product
    Discover our top product CRX Primary Antibody
  • 应用备注
    Optimal dilution of the CRX antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL
    限制
    仅限研究用
  • 缓冲液
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    储存条件
    -20 °C
    储存方法
    After reconstitution, the CRX antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原
    CRX (Cone-Rod Homeobox (CRX))
    别名
    CRX (Cone-rod homeobox) (CRX 产品)
    别名
    Xotx5 antibody, Xotx5b antibody, cord2 antibody, crd antibody, otx5 antibody, otx5b antibody, rx antibody, CRX antibody, crx antibody, otx5-b antibody, CORD2 antibody, CRD antibody, LCA7 antibody, OTX3 antibody, Crx1 antibody, otx5-A antibody, cone-rod homeobox antibody, cone-rod homeobox L homeolog antibody, cone-rod homeobox S homeolog antibody, crx antibody, CRX antibody, Crx antibody, crx.L antibody, crx.S antibody
    背景
    Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. 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.
    UniProt
    O43186
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