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LOR 抗体

LOR WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2462467
发货至: 中国
  • 抗原 See all LOR 抗体
    LOR (Loricrin (LOR))
    适用
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    宿主
    • 22
    • 3
    克隆类型
    • 24
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    多克隆
    标记
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    This LOR antibody is un-conjugated
    应用范围
    • 25
    • 13
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    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    纯化方法
    Antibody is purified by protein A chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LOR.
    Top Product
    Discover our top product LOR Primary Antibody
  • 应用备注
    LOR antibody can be used for detection of LOR by ELISA at 1:62500. LOR antibody can be used for detection of LOR by western blot at 5.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store LOR antibody at -20 °C.
  • 抗原
    LOR (Loricrin (LOR))
    别名
    LOR (LOR 产品)
    别名
    AI036317 antibody, S77319 antibody, RGD1559993 antibody, LOR antibody, loricrin antibody, Loricrin antibody, LOR antibody, Lor antibody, TVAG_146950 antibody, TVAG_228830 antibody, TVAG_228920 antibody, TVAG_238290 antibody, TVAG_035050 antibody, TVAG_070680 antibody, Bm1_52290 antibody, LOC100281109 antibody, LOC100281170 antibody
    物质类
    Chemical
    背景
    LOR is a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.LOR encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in LOR may be the cause of both Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.
    分子量
    35 kDa
    基因ID
    4014
    NCBI登录号
    NP_000418
    UniProt
    P23490
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