The pCLAMP™ Software Suite is an industry-leading patch-clamp electrophysiology data acquisition and analysis program for the control and recording of voltage-clamp, current-clamp, and patch-clamp experiments. The software suite consists of Clampex 11 Software for data acquisition, AxoScope 11 Software for background recording, Clampfit 11 Software for data analysis, and optional Clampfit Advanced Analysis Module for sophisticated and streamlined analysis.
*Supports all previous versions in a model line.
**We only support Professional, Enterprise, and Ultimate editions but not Home edition.
Axon™ pCLAMP®, Axon™ DigiData™ and Windows Operating System Compatibility Table
Consult the table below to determine pCLAMP software compatibility with various AXON digitizers and Windows operating systems.
pCLAMP |
MiniDigi |
DigiData 1200 |
DigiData 132x |
DigiData 1440 |
Digidata 1550 series |
Windows OSa |
8.xb |
No |
Yes |
Yes |
No |
No |
95, 98, ME, NT4.0, 2000, XP |
9.xc |
Yes |
Yes |
Yes |
No |
No |
98, ME, 2000, XP |
10.xd |
Yesh |
No |
Yesg |
Yesf |
Yesf |
2000, XP sp3, Vista, Windows 7 & Windows 10e (32 & 64-bit) |
11.x |
Yesh |
No |
No |
Yes |
Yes |
Windows 7 & Windows 10e (32 & 64-bit) |
Notes:
a.) Only U.S. versions of Windows operating systems are fully supported, and only a computer with authentic Windows is supported, i.e., emulators and virtual machines are not supported. pCLAMP version 10.3 or higher are the only installers that support 64-bit Operating Systems.
b.) Update from 8.0 or 8.1 to 8.2 is free. Only the 32-bit installer of 8.2 runs on Windows XP (see download link above).
c.) Update from 9.0 or 9.1 to 9.2 is free. pCLAMP 9 software is not supported for use under Windows 7 (32- or 64-bit versions).
d.) All updates within 10.x (e.g. from 10.0 to 10.7) are free.
e.) Windows Home Edition is not supported.
f.) Digidata 1440, 1550, 1550A, and 1550B are supported on 10.7.
g.) Use of the Digidata 1320A, 1321A or 1322A on 64-bit Operating Systems is not supported. The Digidata 132x series are only supported up to pCLAMP versions 10.3.
h.) MiniDigi 1B is required for use under 64-bit Operating Systems.
Customer Breakthrough
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Customer Breakthrough
The Zoidl lab at York University, Canada, investigates the roles of pannexin channels in the nervous system in both physiological and pathological contexts, primarily using z…
Brochure
The Axon Instruments® portfolio provides comprehensive solutions for patch-clamping that includes amplifiers, digitizer, software, and accessories.
Customer Breakthrough
Dr. Lauren French is working with undergraduate students at Allegheny College to find out how the amyloid beta peptide implicated in Alzheimer’s disease pathology inhibits a calcium-…
User Guide
The Axon Guide, a guide to electrophysiology and Biophysics laboratory techniques
Customer Breakthrough
The goal of these studies is to identify mechanisms that are amenable to therapeutics and therefore applicable for preventing memory loss. Dr. Krishnan investigates differential phos…
Data Sheet
The Axon™ pCLAMP™ Software Suite from Molecular Devices is the most widelyused electrophysiology data acquisition and analysis program for control and recording of voltage-clamp, cur…
For the latest featured videos, webinars and tutorials on our Axon instrument solution including Axon Patch-clamp Amplifiers, Digidata 1550B Digitizer plus HumSilencer, and pCLAMP Software Suite, visit our Axon Patch-Clamp Video Gallery.
Discover what's new in our Axon Guide
Tech Tips with Jin Yan: User List in Clampex 11
Streamlining electrophysiology data acquisition and analysis in ion channel study with Axon pCLAMP 11 software
Enhance your Electrophysiology studies with Axon pCLAMP 11 Software
Speed up precise data measurements with pCLAMP 11
Empower electrophysiology data analysis with new Clampfit 11 Advanced Event
Empower your electrophysiology studies using new Axon pCLAMP 11 software
Tech Tips with Jin Yan: Sequencing Keys
Tech Tips with Jin Yan: Increasing the number of epochs in Clampex 11
Tech Tips with Jin Yan: Protocol Length in Clampex 11
Save your time on data analysis with new Batch Analysis feature in Axon pCLAMP 11 Software
Tech Tips with Jeffrey Tang: Axon pCLAMP™ 11 Software Feature for Batch Analysis
Tech Tips with Jin Yan: Axon pClamp™ 11 Software Feature for Action Potential Analysis
pCLAMP 11
Enhanced Protocol Editor in pCLAMP 11
Population Spike Analysis in pCLAMP 11
Batch Data Analysis Macros
Neuronal Action Potential Analysis
How to Combine Traces, Calculate Rise or Decay Time Constant, and Perform Curve Fitting Using Axon pCLAMP Software
Update and Hardware Choices for Optogenetics Considerations for Synchronized Light Patterning
Investigations of the Effects of Amyloid-Beta Proteins on hSlo1.1, a BK Channel, in a Xenopus Oocyte Model
Nanopores-Electronic Tools for Single-Molecule Biophysics and Bio-Nanotechnologies
Latest Citations: For a complete list, please click here .
*Source: https://scholar.google.com/
By means of data sampling interface and analysis software of PCLAMP microcomputer processing system, Neural discharge signal was sampled and analyzed. Xetting some parameters of sampling parameter's table and analysis parameter's table of FETCHEX,neural discharge signal was Xampled,and analyzed the signal automatically.Using this method ,the neural discharge in rostral ventrolateral medulla in rat was analyzed, the result was satisfactory.
Using blind whole cell recording technique on rat hippocampal slices, the function and mechanisms of P/N leak subtraction of Clampex program in pClamp acquisition software were studied. The ways of picking up sub-pulse current and properly selecting parameters, including time course, polarization, sub-holding potential, numbers and location of P/N sub-pulse were analyzed in detail. Our results indicate that voltage-gated ion channel currents recorded by Clampex will be more accurate and reproducible by properly using P/N leak subtraction.
The patch-clamp technique has been used to investigate single-channel and whole cell conductances in freshly isolated rat hepatocytes. Whole cell experiments, with high (144 mM) intracellular and extracellular potassium as the principal conductive species, show some variation between cells in the current-voltage relationship (mean whole-cell conductance at physiological potentials being 2.7 nS). This may suggest functional heterogeneity of cells. The most common finding is that the current-voltage relationship shows inward rectification. This is reflected in cell-attached single-channel recordings in which channels displaying strong inward rectification and K+ selectivity are seen. The channels show a mean inward conductance (with 144 mM potassium in the pipette) of 44 pS and an outward conductance of 23 pS. The open probability is not voltage dependent, and the channels do not exhibit calcium dependence. The channels are quite different from others described in hepatocytes, but they show marked similarities to channels recently described in renal epithelial cells. Current-voltage relationships in the whole cell mode exhibit an increase in slope conductance at large hyperpolarizing and depolarizing potentials.