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LCA5 抗体 (HRP)

LCA5 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal HRP
产品编号 ABIN1423582
发货至: 中国
  • 抗原 See all LCA5 抗体
    LCA5 (Leber Congenital Amaurosis 5 (LCA5))
    适用
    • 24
    • 17
    • 16
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 24
    克隆类型
    • 24
    多克隆
    标记
    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LCA5 antibody is conjugated to HRP
    应用范围
    • 20
    • 13
    • 6
    • 2
    • 2
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human LCA5
    亚型
    IgG
    Top Product
    Discover our top product LCA5 Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    注意事项
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    LCA5 (Leber Congenital Amaurosis 5 (LCA5))
    别名
    LCA5 (LCA5 产品)
    别名
    C6orf152 antibody, RGD1308555 antibody, 4930431B11Rik antibody, 5730406O13Rik antibody, AV274874 antibody, ORF64 antibody, LCA5, lebercilin antibody, Leber congenital amaurosis 5 antibody, Leber congenital amaurosis 5 (human) antibody, LCA5 antibody, LOC787523 antibody, Lca5 antibody
    背景

    Synonyms: C6orf152, LCA5, Leber congenital amaurosis 5, Leber congenital amaurosis 5 protein, ORF64, RGD1308555.

    Background: Leber congenital amaurosis (LCA) is one of the most common causes of hereditary blindness or severe visual impairment in infants. Mutations in several genes with diverse functions mapping to two loci have been implicated in LCA causation. These proteins are involved in processes such as photoreceptor development and maintenance, phototransduction, vitamin A metabolism and protein trafficking. LCA5, also known as Lebercilin, is a ciliary protein that is widely expressed during development and localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.

    基因ID
    167691
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