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- 服务名称:
突触可塑性PCR基因芯片
- 提供商:
SABiosciences
技术服务网址:http://www.yingbio.com/
服务热线:400-696-6643、 18019265738
邮箱:daihp@yingbio.com 、 huizhang1228@foxmail.com
Synaptic Plasticity PCR Array
突触可塑性PCR基因芯片
| Product | Species | Technology | Cat. No. |
| Synaptic Plasticity PCR Array | Human | Gene Expression | PAHS-126Z |
| Synaptic Plasticity PCR Array | Mouse | Gene Expression | PAMM-126Z |
| Synaptic Plasticity PCR Array | Rat | Gene Expression | PARN-126Z |
Synaptic Plasticity RT² Profiler™ PCR Array profiles the expression of 84 key genes central to synaptic alterations during learning and memory. The brain recalls immediate events via short-term memories; however, it must consolidate these events into long-term memory for later recall. Memory consolidation requires synaptic plasticity characterized by physical changes to, and gene expression changes in, neuronal synapses. Synaptic plasticity studies have discovered immediate-early genes (IEGs) that alter expression immediately after neuronal events. IEGs mediate long-term potentiation (LTP), a process that enhances synaptic connections and consolidates memories. However, as not all events become long-term memories, the opposite synaptic remodeling response, long-term depression (LTD), also plays a central role in synaptic plasticity. Gene expression changes associated with LTD yield physical changes in the neuronal synapse that recycle receptors and either enhance or inhibit synaptic connections. This array includes IEGs and other genes important for LTP and LTD, as well as key neuronal receptor genes and genes important for synapse remodeling. Using real-time PCR, you can easily and reliably analyze the expression of a focused panel of genes involved in synaptic plasticity, LTP and LTD with this array.
突触可塑性PCR基因芯片可以同时检测学习和记忆过程中参与突触改变的84个关键基因的表达。对于回忆,大脑可以有两种方式记录以往事件:短期记忆和长期记忆。其中长期记忆需要突触物理性的改变,并伴有神经突触相关基因表达的变化。突触可塑性的研究已经发现神经元的活动变化后,即早基因(IEGs)的表达立即改变。IEGs介导的长时程增强(LTP)可以增强突触连接并巩固记忆。然而并非所有事件都成为长期记忆,相反的突触重塑反应(长时程抑制,LTD),在突触可塑性也起到了核心作用。LTD相关基因的表达变化可以改变神经元突触受体的循环,从而增强或抑制突触连接。该芯片包含IEGs,其他参与LTP和LTD的重要基因,以及参与突触重塑的关键受体基因等。利用实时定量PCR,研究者可以方便并且可信地对参与突触可塑性的相关基因进行同时检测。
Immediate-Early Response Genes (IEGs):ARC, BDNF, CEBPB, CEBPD, CREB1, CREM, EGR1, EGR2, EGR3, EGR4, FOS, HOMER1, JUN, JUNB, KLF10, MMP9 (Gelatinase B), NFKB1, NFKBIB (TRIP9), NGF, NPTX2, NR4A1, NTF3, PCDH8, PIM1, PLAT (tPA), RELA, RGS2, RHEB, SRF, TNF.
Late Response Genes:INHBA, SYNPO.
Long Term Potentiation (LTP):ADCY1, ADCY8, BDNF, CAMK2A, CAMK2G, CDH2 (N-cadherin), CNR1, GABRA5, GNAI1, GRIA1, GRIA2, GRIN1, GRIN2A, GRIN2B, GRIN2C, GRIN2D, MAPK1, MMP9 (Gelatinase B), NTF4, NTRK2, PLCG1, PPP1CA, PPP1CC, PPP3CA, PRKCA, PRKCG, RAB3A, YWHAQ (14-3-3).
Long Term Depression (LTD):GNAI1, GRIA1, GRIA2, GRIA3, GRIA4, GRIP1, GRM1, GRM2, IGF1, MAPK1, NOS1, NGFR, PICK1, PLAT (tPA), PPP1CA, PPP1CC, PPP1R14A (CPI-17), PPP2CA, PPP3CA, PRKCA, PRKG1.
Cell Adhesion:ADAM10, CDH2 (N-cadherin), GRIN2A, GRIN2B, NCAM1, PCDH8, PPP2CA, RELN, TNF.
Extracellular Matrix & Proteolytic Processing:ADAM10, MMP9 (Gelatinase B), PLAT (tPA), RELN, TIMP1.
CREB Cofactors:AKT1, CAMK2G, GRIN1, GRIN2A, GRIN2B, GRIN2C, GRIN2D, MAPK1 (ERK2), PPP1CA, PPP1CC.
Neuronal Receptors:EPHB2, GABRA5, GRIA1, GRIA2, GRIA3, GRIA4, GRIN1, GRIN2A, GRIN2B, GRIN2C, GRIN2D, GRM1, GRM2, GRM3, GRM4, GRM5, GRM7, GRM8, NTRK2.
Postsynaptic Density: ADAM10, ARC, DLG4 (PSD95), GRIA1, GRIA3, GRIA4, GRIN1, GRIN2A, GRIN2B, GRIN2C, GRM1, GRM3, HOMER1, PICK1, SYNPO.
Others:KIF17, SIRT1.
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文献和实验提供的PCR Array产品举例 订制的PCR芯片 如果现有的产品无法满足研究者的特定需要,SuperArray还可以提供从设计到芯片生产的完整服务,为研究者提供使用先进的PCR芯片的便捷服务。客户订制芯片服务为研究者提供以下便利:1)在使用表达谱基因组芯片后,对从基因组水平筛选出来的一组基因进行验证;2)在现有产品的基础上作适当调整以适应特殊需要;3)完全从头设计,适用于在现有的预设计PCR芯片中尚未包括的某个信号通路或者一组基因。若研究基因数目少于84个,还可以将96孔PCR芯片进一步分成
【求助】什么是micro-array analysis,怎么翻译?
and Design of Micro-array PCR Chip Scanner 微阵列PCR基因芯片扫描仪的研制 Image Signal Acquisition System for SPR Micro-Array Based on Phase Detection SPR微阵列相位检测图像信息采集系统研究 Development of Imaging SPR Analyzer and Its Micro-array
liuwenbinahslyy 基因芯片数据分析时,比值大于2.0或者小于0.5被认为是有表达差异,为什么要相差两倍呢?这个比值与PCR或Western blot验证时的基因或蛋白表达差异是否是一致的(即是否也是相差两倍以上)?按理说PCR或Western blot检测表达差异根本不需要相差两倍以上,这还取决于重复实验的次数及数据的分布情况。 zjubell liuwenbinahslyy wrote









