merck millipore,默克密理愽
  • merck millipore,默克密理博,16-321,Anti-Ras Magnetic Bead Conjugate Antibody

  • merck millipore,默克密理博,16-321,Anti-Ras Magnetic Bead Conjugate Antibody

    产品名称：Anti-Ras Magnetic Bead Conjugate Antibody
    产品型号：16-321
    Anti-Ras Magnetic Bead Conjugate Antibody detects level of Ras Magnetic Bead Conjugate & has been published & validated for use in WB & IP.

    merck millipore,默克密理博,16-321,Anti-Ras Magnetic Bead Conjugate Antibody

  • 产品介绍
  • merck millipore,默克密理博,16-321,Anti-Ras Magnetic Bead Conjugate Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    M, H, RWBMPurifiedMonoclonal Antibody
    描述
    产品目录编号 16-321
    描述 Anti-Ras Magnetic Bead Conjugate Antibody
    Alternate Names
    • v-Ha-ras Harvey rat sarcoma viral oncogene homolog
    • GTP- and GDP-binding peptide B
    • GTPase Hras
    • Ha-Ras1 proto-oncoprotein
    • Ras family small GTP binding protein H-Ras
    • Transforming protein p2
    • c-has/bas p21 protein
    • c-ras-Ki-2 activated oncogene
    • p19 H-RasIDX protein
    • transformation gene: oncogene HAMSV
    背景信息 The tumor oncoproteins HRas, KRas, and NRas are rated as Ras protoncogenes. Point mutations within Ras genes are frequently detected in human malignancies and in experimentally induced tumors in animals.
    产品信息
    格式 Purified
    控制
    • A431 whole cell lysate
    演示 20% slurry; 1xPBS, 0.05% sodium azide. Sufficient for 10 immunoprecipitation assays.
    应用
    应用 Anti-Ras Magnetic Bead Conjugate Antibody detects level of Ras Magnetic Bead Conjugate & has been published & validated for use in WB & IP.
    主要应用
    • Western Blotting
    应用说明 Immunoprecipitation:
    150 μg of this antibody has been reported to immunoprecipitate Ras.
    生物信息
    免疫原品种 KLH-conjugated protein corresponding to human Ras.
    宿主 Mouse
    特异性 This antibody recognizes p21H-, K- and N-Ras.
    同种型 IgG2aκ
    品种反应性 MouseHumanRat
    Species Reactivity Note Proven to react with human, mouse and rat. Other species unknown.
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NP_203524
    Entrez基因汇总 Members of the RAS superfamily of GTP-binding proteins, which includes MRAS, are membrane-anchored, intracellular signal transducers responsible for a variety of normal cellular functions. They are oncogenically activated in a significant fraction of tumors.[supplied by OMIM]
    基因符号
    • ALPS4
    • K-Ras
    • Ki-Ras
    • K-Ras2
    • Kras-2
    • p21B
    • KRAS
    • RASK2
    • HRAS
    • HA_RAS
    • N-RAS
    • H-RAS
    • NRAS
    • NRAS1
    纯化方法 Protein G purfied
    UniProt编号
    • P01116
    UniProt汇总 FUNCTION: Ras proteins bind GDP/GTP and possess intrinsic GTPase activity.
    Enzyme regulation:Alternate between an inactive form bound to GDP and an active form bound to GTP. Activated by a guanine nucleotide-exchange factor (GEF) and inactivated by a GTPase-activating protein (GAP).
    SIZE: 189 amino acids; 21,656 Da
    SUBUNIT: Interacts with PHLPP (By similarity).
    SUBCELLULAR LOCATION: Cell membrane; Lipid-anchor; Cytoplasmic side.
    Involvement in disease:
    Defects in KRAS are a cause of acute myelogenous leukemia (AML) [MIM:601626]. AML is a malignant disease in which hematopoietic precursors are arrested in an early stage of development.

    Defects in KRAS are a cause of juvenile myelomonocytic leukemia (JMML) [MIM:607785]. JMML is a pediatric myelodysplastic syndrome that constitutes approximately 30% of childhood cases of myelodysplastic syndrome (MDS) and 2% of leukemia. It is characterized by leukocytosis with tissue infiltration and in vitro hypersensitivity of myeloid progenitors to granulocyte-macrophage colony stimulating factor.

    Defects in KRAS are the cause of Noonan syndrome 3 (NS3) [MIM:609942]. Noonan syndrome (NS) [MIM:163950] is a disorder characterized by dysmorphic facial features, short stature, hypertelorism, cardiac anomalies, deafness, motor delay, and a bleeding diathesis. It is a genetically heterogeneous and relatively common syndrome, with an estimated incidence of 1 in 1000-2500 live births. Rarely, NS is associated with juvenile myelomonocytic leukemia (JMML). NS3 inheritance is autosomal dominant.

    Defects in KRAS are a cause of cardiofaciocutaneous syndrome (CFC syndrome) [MIM:115150]; also known as cardio-facio-cutaneous syndrome. CFC syndrome is characterized by a distinctive facial appearance, heart defects and mental retardation. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. The inheritance of CFC syndrome is autosomal dominant.

    KRAS mutations are involved in cancer development.
    产品使用声明
    使用声明
    • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    储存和货运信息
    存储条件 Stable for 1 year at 2-8ºC from date of receipt.
    DO NOT FREEZE
    包装信息
    数量 200 µL

    merck millipore,默克密理博,16-321,Anti-Ras Magnetic Bead Conjugate Antibody

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