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CX3CR1 Protein-VLP, Human, Recombinant (Flag & Strep) is expressed in HEK293 Cells. The accession number is P49238.
规格 | 价格 | 库存 | 数量 |
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生物活性 | Immobilized CX3CR1 Protein-VLP, Human, Recombinant (Flag & Strep)) (Cat#TMPY-07102) at 5 μg/mL (100 μL/well) can bind Anti-CX3CR1 Monoclonal antibody, heavy chain antibody, Human IgG1, the EC50 is 0.5-5 ng/mL. |
产品描述 | CX3CR1 Protein-VLP, Human, Recombinant (Flag & Strep) is expressed in HEK293 Cells. The accession number is P49238. |
种属 | Human |
表达系统 | HEK293 Cells |
标签 | N-Flag, C-Strep |
蛋白编号 | P49238 |
蛋白构建 | A DNA sequence encoding the Human CX3CR1-VLP (P49238) (Met1-Leu315,thermostabilizing mutations) was expressed, with a Flag tag at the N-terminus, and a strep tag at the C-terminus. |
分子量 | 40.4 kDa (predicted) |
内毒素 | < 1.0 EU per μg protein as determined by the LAL method. |
缓冲液 | Supplied as sterile 50 mM Hepes, 150 mM NaCl, 10% Trehalose, pH 7.2. Please contact us for any concerns or special requirements. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA. |
存储 | Samples are stable for up to twelve months from date of receipt at -70℃. Store it under sterile conditions at -70℃ or lower. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
运输方式 | It is supplied and shipped as liquid with dry ice. |
研究背景 | The CX3C chemokine axis consists of fractalkine (CX3CL1) and its receptor (CX3CR1); these are expressed by neurons and microglia respectively, and are known to modulate microglial activation. Neuronal Cx3cr1 may impact Alzheimer's disease-like pathology by modulating conformational state-dependent amyloid-beta-induced synaptotoxicity. Microglial cells participate in brain development and influence neuronal loss and synaptic maturation. Fractalkine is an important neuronal chemokine whose expression increases during development and that can influence microglia function via the fractalkine receptor, CX3CR1. Mice lacking Cx3cr1 show a variety of neuronal defects thought to be the result of deficient microglia function. Knockout of the microglial chemokine receptor Cx3cr1 to prevent neuron loss. |
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