Mouse NGF Premium Research Pack

Mouse NGF Premium Research Pac

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  • $1138
  • Alomone
  • ZK-0039542
  • 以色列
  • 2025年11月20日
  • 见官方网站
  • 见 说 明 书
  • 见官方网站
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  • 企业认证

    • 详细信息
    • 技术资料
    • 供应商

      上海再康生物科技有限公司

    • 库存

      大量

    • 靶点

      见官方网站

    • 级别

    • 目录编号

      ESP-651

    • 克隆性

      多克隆

    • 抗原来源

      见 说 明 书

    • 保质期

      6个月

    • 抗体英文名

      Mouse NGF Premium Research Pack

    • 抗体名

      Mouse NGF Premium Research Pack

    • 标记物

      见官方网站

    • 宿主

      见 说 明 书

    • 适应物种

      见官方网站

    • 免疫原

      见官方网站

    • 亚型

      见官方网站

    • 形态

      液体或冻干粉

    • 应用范围

      见官方网站

    • 浓度

      见官方网站

    • 保存条件

      -20°C

    • 规格

      9 Vials

    Mouse NGF Premium Research Pack

    All You Need for NGF Research
    Cat #: ESP-651
    9 Vials

    Alomone Labs is pleased to offer the Mouse NGF Premium Research Pack (#ESP-651). The Research Pack contains all you need for human NGF research: Antibodies to NGF and its receptors, natural NGF and a specific TrkA receptor inhibitor all in one economical package!

    • Compounds
    • Scientific Background
    • Related Products
    Product Name Cat # Size
    Mouse NGF/proNGF Neutralizing Antibody
    ALM-006 1 x 0.25 mg
    Anti-mNGF
    AN-240 1 x 0.2 ml
    Anti-p75NTR (extracellular)
    ANT-007 1 x 0.2 ml
    Anti-TrkA (extracellular)
    ANT-018 1 x 0.2 ml
    GW441756 hydrochloride
    G-191 1 x 25 mg
    mouse NGF 2.5S (>95%)
    N-100 1 x 0.1 mg

    Note A mouse monoclonal antibody (#ALM-006) is included in this Research Pack. Please take into account when reacting with a secondary antibody.
    Scientific Background 

    The neurotrophins ("neuro" means nerve and "trophe" means nutrient) are a family of soluble, basic growth factors which regulate neuronal development, maintenance, survival and death in the CNS and the PNS.1 NGF, the first member of the family to be discovered, was originally purified as a factor able to support survival of sympathetic and sensory spinal neurons in culture.2 It is synthesized and secreted by sympathetic and sensory target organs and provides trophic support to neurons as they reach their final target.3 Neurotrophin secretion also increases in the nervous system following injury. Schwann cells, fibroblasts, and activated mast cells normally synthesize NGF constitutively, however direct trauma and induced cytokines combine to increase neurotrophin production in these cells after injury.4 

    NGF is purified in three forms: the 7S, 2.5S and β. The 7S, 130 kDa, form occurs naturally in mouse submaxillary glands, and is a multimeric protein composed of two α, one β and two γ subunits. The name is derived from its sedimentation co-efficient, 7S. The biologically active subunit is the β, which is a 26 kDa dimer composed of two identical 120 amino acid chains held together by hydrophobic interactions.5 The 2.5S form is 9 amino acids shorter than the β form, because of proteolysis that occurs during the purification process.6 The structural hallmark of all the neurotrophins is the characteristic arrangement of the disulfide bridges known as the cysteine knot, which has been found in other growth factors such as PDGF.7 There is a 95.8% homology between the rat and mouse forms, and a 85% homology between the human and mouse. 

    NGF has been shown to regulate neuronal survival, development function and plasticity.8 Recently, involvement of NGF in processes not involving neuronal cells has been shown, such as asthma,9 psoriasis10 and wound healing.11  

    The biological effects of NGF are mediated by two receptors: TrkA, which is specific for NGF, and p75, which binds all the neurotrophins.12


    Mouse NGF Premium Research PackReferences 
    1. Roux, P. and Barker P. A. (2002) Prog. Neurobiol. 67, 203.
    2. Levi-Montalcini, R. (1966) Harvey Lect. 60, 217.
    3. Farinas, I. et al. (1998) Neuron 21, 325.
    4. Levi-Montalcini, R. et al. (1996) Trends Neurosci. 19, 514.
    5. Bradshaw, R.A. (1978) Ann. Rev. Biochem 47, 191.
    6. Bocchini, V. and Angeletti, P.U. (1969) Proc. Natl. Acad. Sci. U.S.A. 64, 787.
    7. McDonald, N.Q. et al. (1991) Nature 354, 411.
    8. Huang, E.J. and Reichardt, L.F. (2001) Annu. Rev. Neurosci. 24, 677.
    9. Freund, V. and Frossard, N. (1994) Prog. Brain Res. 146, 335.
    10. Raychaudhuri, S.P. and Raychaudhuri, S.K. (2004) Prog. Brain Res. 146, 433.
    11. Kawamoto, K. and Matsuda, H. (2004) Prog. Brain. Res. 146, 369.
    12. Teng, K.K. and Hempstead, B.L. (2004) Cell Mol. Life Sci. 61, 35.

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