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p21 Ras (HRAS) Mouse Monoclona

l Antibody [Clone ID: LBI1G8]
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  • ¥3300
  • Leading Biology
  • 美国
  • 2025年07月14日
  • WB 1:2000, IF 1:100
  • Mouse
  • Human, Mouse, Rat
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 靶点

      HRAS

    • 应用范围

      WB 1:2000, IF 1:100

    • 宿主

      Mouse

    • 适应物种

      Human, Mouse, Rat

    • 保质期

      1-2年

    • 供应商

      安诺伦(北京)生物科技有限公司

    • 标记物

      Unconjugated

    • 克隆性

      Monoclonal Antibody

    • 保存条件

      Stable for 1 year at -20°C from date of shipment. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

    • 形态

      Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

    • 亚型

      IgG1

    • 免疫原

      Full length human recombinant protein of human HRAS(NP_005334) produced in HEK293T cell.

    • 规格

      100 ug

    别名:C-BAS/HAS; C-H-RAS; C-HA-RAS1; CTLO; H-RASIDX; HAMSV; HRAS1; p21ras; RASH1

    产品概述:Carrier-free (BSA/glycerol-free) HRAS mouse monoclonal antibody,clone LBI1G8

    总结:This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, mental retardation, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma. Multiple transcript variants, which encode different isoforms, have been identified for this gene. [provided by RefSeq, Jul 2008]

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    图标文献和实验
    相关实验
    • 丁香园引物库(2004-10-13更新)

      of DNA binding 1, dominant negativehelix-loop-helix protein/NM_002165 striated muscle contraction regulatory protein (Id2B ) / NM_002166 nucleobindin 2/ NM_005013 calreticulin/NM_004343 polycystic kidney disease 2 (autosomal dominant)/ NM_000297 RAS

    • [资源] 所有的看家基因(housekeeping genes)列表+引物设计服务

      Homo sapiens RAP1B, member of RAS oncogene family (RAP1B), mRNA 736 NM_016532 Homo sapiens skeletal muscle and kidney enriched inositol phosphatase (SKIP), transcript variant 1, mRNA 1529 NM_015292 Homo sapiens likely ortholog of mouse membrane

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