电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

LCA5 抗体 (N-Term)

LCA5 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN632308
发货至: 中国
  • 抗原 See all LCA5 抗体
    LCA5 (Leber Congenital Amaurosis 5 (LCA5))
    抗原表位
    • 6
    • 1
    • 1
    • 1
    • 1
    N-Term
    适用
    • 25
    • 18
    • 17
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 25
    克隆类型
    • 25
    多克隆
    标记
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LCA5 antibody is un-conjugated
    应用范围
    • 21
    • 13
    • 6
    • 3
    • 2
    Western Blotting (WB)
    特异性
    LCA5 antibody was raised against the N terminal of LCA5
    纯化方法
    Affinity purified
    免疫原
    LCA5 antibody was raised using the N terminal of LCA5 corresponding to a region with amino acids FSLQKLKEISEARHLPERDDLAKKLVSAELKLDDTERRIKELSKNLELST
    Top Product
    Discover our top product LCA5 Primary Antibody
  • 应用备注
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    LCA5 Blocking Peptide, catalog no. 33R-3071, is also available for use as a blocking control in assays to test for specificity of this LCA5 antibody

    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of LCA5 antibody in PBS
    浓度
    Lot specific
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 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
    LCA5 is a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Mutations in this gene cause Leber congenital amaurosis type V. Alternative splicing results in two transcript variants.
    分子量
    80 kDa (MW of target protein)
You are here:
客服