SyncroPatch 384全自动膜片钳系统
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SyncroPatch 384全自动膜片钳系统

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  • 询价
  • nanion
  • 德国
  • SyncroPatch 384
  • 2025年07月15日
    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 库存

      大量

    • 供应商

      耐尼恩

    • 现货状态

      有货

    • 保修期

      一年

    • 规格

      384通道/768通道

    SyncroPatch 384高通量全自动膜片钳系统

    新型 SyncroPatch 384 是一种革命性的全自动膜片钳系统,由集成有先进的液体处理系统 Biomek i5 的膜片钳模块组成。 使用 384 通道放大器和一个 384通道移液头,所有384 个细胞都被并行记录,从而产生每天 20,000 个数据点的通量。得益于其易用性和开放式设计,SyncroPatch 384 支持完全自动化并集成到 HTS 环境中。

    但 SyncroPatch 384 不仅仅是一个高通量筛选系统,而且可以在您的所有电生理学项目中实施,无论您的通量需求如何。 32 孔操作模式非常适合较小的筛选项目和学术研究,并充分利用了经济实惠的NPC-384芯片。 以 32 的倍数选择您需要并行记录的孔数,您可以在几天内使用剩余的孔。 或者,您可以使用 SyncroPatch 384 进行长达8 小时的无人值守模式的全自动实验。

    数据质量和灵活性使 SyncroPatch 384 成为制药公司、CRO 和学术机构等需要的384通道全自动膜片钳系统。

    主要特征

    • 千兆级封接记录
    • 384孔平行记录
    • 32孔模式适用于较少的化合物筛选和研究项目
    • 通常成功率达到>85%
    • 用于快速脱敏配体门控离子通道的快速外液更换(高达110 µl/s)
    • 记录时的內液灌流——通过內液激活通道,例如钙激活K+通道。
    • 高级温度控制可以使实验过程中降低或升高的温度(范围10-37°C)标准化
    • 具有电流钳功能的基本特点
    • 单孔芯片用于高表达细胞系,多孔芯片用于低表达细胞系。 所有芯片都是通过室内质控生产
    • 可以收集样品数据进行量效曲线分析
    • 受益于良好的服务和技术支持

    PatchControl 384

    PatchControl 384是一个功能强大的图形用户界面,用于直观、快速、轻松地设置电压协议和实验参数。记录井根据用户定义的质量标准(例如密封电阻、串联电阻或电容)进行可视化和颜色编码。单击鼠标一次,视图切换到在线分析结果,例如I/V曲线或浓度响应曲线。


    DataControl384:分析软件

    DataControl 384用于可视化和分析PatchControl 384数据,采用用户定义的数据分析模板。结果(自动IC50、EC50、IV关系图生成)、复合信息和质量控制参数以用户定义的导出格式一起导出,自动生成pdf报告,并为进一步的数据库集成准备数据。这一过程简单、直观且快速完成。

    NPC-384

    NPC-384芯片是SyncroPatch 384的高性价比和高质量耗材。它在慕尼黑的Nanion总部内部生产,质量有保证。可提供不同类型的NPC-384芯片,应根据单元大小和应用选择。

    带有贴片孔的硼硅酸盐玻璃载玻片封装在384孔板中,形成孔,在孔板中输送电池和外部溶液。芯片的设计允许在实验过程中灌注内部溶液。每个NPC-384芯片包含384个记录室。这些站点可以一次性使用,也可以在32井模式下使用,部分芯片可以在32的倍数下使用,其余部分可以在数天内使用,不会降低成功率。在SyncroPatch 384上可以测量一个芯片,在机器人上可以堆叠25个芯片进行无人值当实验。芯片的开放性设计使样品的采集和化合物浓度的后续验证成为可能。此外,内部或外部解决方案的交换次数是无限的。NPC-384芯片可用于GOhm密封的单井眼,也可用于单井眼,以增加测量电流幅值,提高成功率。

    Available chip types

    • "NPC-384, 1x medium resistance": One hole per well (Order # 221102)

    • "NPC-384, 1x medium resistance plus": One hole per well (Order # 221104)

    • "NPC-384, 4x medium resistance": 4 holes per well (Order # 221402)

    • "NPC-384, 1x high resistance": One hole per well (Order # 221101)

    • "NPC-384, 4x high resistance": 4 holes per well (Order # 221401)

    • "NPC-384, 1x low resistance": One hole per well (Order # 221103)

    • "NPC-384, 4x low resistance": 4 holes per well (Order # 221403)

    • "NPC-384, 8x": 8 holes per well (Order # 221801)

    SyncroPatch 384/384i/768i的缓冲液和解决方案
    可靠的缓冲溶液对于任何电生理应用都至关重要。因此,我们的目标是提供合适的解决方案,让您对质量和稳定性毫无疑问。我们的质量保证包括化学测试以及每批膜片钳系统的测试。我们的缓冲器随附相应的“分析证书”和“材料安全数据表”(MSDS)。

    Available buffers and solutions

    • "External Standard", 500 mL: (Order # 08 3001)

    • "External Standard Ca 10", 500 mL: (Order # 08 3012)

    • "External NMDG 60", 500 mL: (Order # 08 3004)

    • "External NMDG 60 Ca 10", 500 mL: (Order # 08 3011)

    • "External [-] Ca2+ [-] Mg2+", 500 mL: (Order # 08 3003)

    • "Internal CsF 110", 500 mL: (Order # 08 3008)

    • "Internal KF 110", 500 mL: (Order # 08 3007)

    • "Washing solution", 5 L: (Order # 08 3010)

    2022海报:





    发表文献:

    2022 - Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel NaV1.5
    2022 - The suitability of high throughput automated patch clamp for physiological applications
    2022 - Pharmacological Dissection of the Crosstalk between NaV and CaV Channels in GH3b6 Cells
    2022 - Ionotropic glutamate receptors: Structure, function and dysfunction
    2022 - In vivo spatiotemporal control of voltage-gated ion channels by using photoactivatable peptidic toxins
    2022 - Identification of positive modulators of TRPM5 channel from a high-throughput screen using a fluorescent membrane potential assay
    2022 - Chemical Synthesis of a Functional Fluorescent-Tagged α-Bungarotoxin
    2022 - Altered Ca2+ Homeostasis in Red Blood Cells of Polycythemia Vera Patients Following Disturbed Organelle Sorting during Terminal Erythropoiesis
    2021 - The Schizophrenia Variant V1282F in SCN2A Causes Functional Impairment of NaV1.2

    2021 - The insecticide deltamethrin enhances sodium channel slow inactivation of human Nav1.9, Nav1.8 and Nav1.7

    2021 - Neurogranin, Encoded by the Schizophrenia Risk Gene NRGN, Bidirectionally Modulates Synaptic Plasticity via Calmodulin-Dependent Regulation of the Neuronal Phosphoproteome

    2021 - Mechanism of hERG inhibition by gating-modifier toxin, APETx1, deduced by functional characterization

    2021 - High-throughput characterization of photocrosslinker-bearing ion channel variants to map residues critical for function and pharmacology

    2021 - Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology

    2021 - From High-Throughput Screening to Target Validation: Benzo[d]isothiazoles as Potent and Selective Agonists of Human Transient Receptor Potential Cation Channel Subfamily M Member 5 Possessing In Vivo Gastrointestinal Prokinetic Activity in Rodents

    2021 - Fluorescent- and tagged-protoxin II peptides: potent markers of the Nav1.7 channel pain target

    2021 - Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy (2)

    2021 - Disease-linked super-trafficking of a potassium channel

    2021 - Differential contributions of M1 and pre-M1 to ion selectivity in ASICs and ENaCs

    2021 - Comprehensive preclinical evaluation of how cardiac safety profiles of potential COVID-19 drugs are modified by disease associated factors

    2021 - Cation and anion channelrhodopsins: Sequence motifs and taxonomic distribution

    2021 - Applying the CiPA Approach to Evaluate Cardiac Proarrhythmia Risk of some Antimalarials Used Off‐label in the First Wave of COVID‐19

    2021 - A Massively Parallel Trafficking Assay Accurately Predicts Loss of Channel Function in KCNH2 Variants

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    • 作者
    • 内容
    • 询问日期
    图标文献和实验
    该产品被引用文献

    2022 - Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel NaV1.5
    2022 - The suitability of high throughput automated patch clamp for physiological applications
    2022 - Pharmacological Dissection of the Crosstalk between NaV and CaV Channels in GH3b6 Cells
    2022 - Ionotropic glutamate receptors: Structure, function and dysfunction
    2022 - In vivo spatiotemporal control of voltage-gated ion channels by using photoactivatable peptidic toxins
    2022 - Identification of positive modulators of TRPM5 channel from a high-throughput screen using a fluorescent membrane potential assay
    2022 - Chemical Synthesis of a Functional Fluorescent-Tagged α-Bungarotoxin
    2022 - Altered Ca2+ Homeostasis in Red Blood Cells of Polycythemia Vera Patients Following Disturbed Organelle Sorting during Terminal Erythropoiesis
    2021 - The Schizophrenia Variant V1282F in SCN2A Causes Functional Impairment of NaV1.2

    2021 - The insecticide deltamethrin enhances sodium channel slow inactivation of human Nav1.9, Nav1.8 and Nav1.7

    2021 - Neurogranin, Encoded by the Schizophrenia Risk Gene NRGN, Bidirectionally Modulates Synaptic Plasticity via Calmodulin-Dependent Regulation of the Neuronal Phosphoproteome

    2021 - Mechanism of hERG inhibition by gating-modifier toxin, APETx1, deduced by functional characterization

    2021 - High-throughput characterization of photocrosslinker-bearing ion channel variants to map residues critical for function and pharmacology

    2021 - Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology

    2021 - From High-Throughput Screening to Target Validation: Benzo[d]isothiazoles as Potent and Selective Agonists of Human Transient Receptor Potential Cation Channel Subfamily M Member 5 Possessing In Vivo Gastrointestinal Prokinetic Activity in Rodents

    2021 - Fluorescent- and tagged-protoxin II peptides: potent markers of the Nav1.7 channel pain target

    2021 - Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy (2)

    2021 - Disease-linked super-trafficking of a potassium channel

    2021 - Differential contributions of M1 and pre-M1 to ion selectivity in ASICs and ENaCs

    2021 - Comprehensive preclinical evaluation of how cardiac safety profiles of potential COVID-19 drugs are modified by disease associated factors

    2021 - Cation and anion channelrhodopsins: Sequence motifs and taxonomic distribution

    2021 - Applying the CiPA Approach to Evaluate Cardiac Proarrhythmia Risk of some Antimalarials Used Off‐label in the First Wave of COVID‐19

    2021 - A Massively Parallel Trafficking Assay Accurately Predicts Loss of Channel Function in KCNH2 Variants

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