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CMA 7 Microdialysis Probes

Store/Surgical/Microdialysis/Probes and Guides/CMA Probes CNS Mouse

Product Details

NEW! CMA 7 PROBES FOR BIG MOLECULES!

The CMA 7 Microdialysis Probe is ideal for use in small areas of the brain or spinal cord of small animals. It is especially suitable for studies in transgenic mice.

Extremely small
Optimized for CNS use
Ideal for chronical implantation
Membrane lengths: 1 or 2 mm
Membrane diameter: 0.24 mm (6 kDa), 0.26 mm (55 kDa) or 0.28 mm (500 kDa or 2 MDa)
Available metal free or β-irradiated

Item Listing

Item#	Description
CMAP000082	CMA 7 6 kDa Microdialysis Probe, 1 mm membrane length (pkg. of 3)
CMAP000083	CMA 7 6 kDa Microdialysis Probe, 2 mm membrane length (pkg. of 3)
CMA8010771	CMA 7 6 kDa Metal Free Microdialysis Probe, 1 mm membrane length (pkg. of 3)
CMA8010772	CMA 7 6 kDa Metal Free Microdialysis Probe, 2 mm membrane length (pkg. of 3)
CMA8010681	CMA 7 6 kDa β-Irradiated Microdialysis Probe, 1 mm membrane length (pkg. of 3)
CMA8010682	CMA 7 6 kDa β-Irradiated Microdialysis Probe, 2 mm membrane length (pkg. of 3)
CMA8012411	CMA 7 55 kDa Microdialysis Probe, 1 mm membrane length, pkg. of 3
CMA8012412	CMA 7 55 kDa Microdialysis Probe, 2 mm membrane length, pkg. of 3
CMA8012421	CMA 7 500 kDa Microdialysis Probe, 1 mm membrane length, pkg. of 3
CMA8012422	CMA 7 500 kDa Microdialysis Probe, 2 mm membrane length, pkg. of 3
CMA8012423	CMA 7 2 MDa Microdialysis Probe, 1 mm membrane length, pkg. of 3
CMA8012424	CMA 7 2 MDa Microdialysis Probe, 2 mm membrane length, pkg. of 3

NEW! CMA 7 PROBES FOR BIG MOLECULES!

The CMA 7 Microdialysis Probe is ideal for use in small areas of the brain or spinal cord of small animals. It is especially suitable for studies in transgenic mice.

The construction and geometry of the CMA 7 6 kDa Microdialysis Probe tip is exactly the same as in the CMA 11. The outer diameter is 0.24 mm and the shaft length is 7 mm.

New CMA 7 microdialysis probes are now available with 55 kDa cut-off and 0.26 mm outer diameter (more details in the Specifications section).

New CMA 7 microdialysis probes for big molecules are also now available with 500 kDa and 2 MDa cut-off, 0.28 mm outer diameter and 14 mm shaft length (more details in the Specifications section).

An extremely small plastic body where the inlet and outlet tubing are directly mounted, makes the probe easy to implant and light for a small animal to carry. A matching small and lightweight guide cannula is available.

Standard part numbers are available for metal free or β-irradiated CMA 7 6 kDa probes.

For metal free or β-irradiated CMA 7 55 kDa, 500kDa and 2MDa probes, please make your request using our Custom Probe Form and send it to our Technical Support Team. We will contact you promptly.

CMA 7 Microdialysis Probes are guaranteed for single use.

Specifications

Specifications	CMAP000082	CMAP000083	CMA8010771	CMA8010772	CMA8010681	CMA8010682	CMA8012411	CMA8012412	CMA8012421	CMA8012422	CMA8012423	CMA8012424
Membrane Length	1 mm	2 mm	1 mm	2 mm	1 mm	2 mm	1 mm	2 mm	1 mm	2 mm	1 mm	2 mm
Membrane O D	0.24 mm	0.24 mm	0.24 mm	0.24 mm	0.24 mm	0.24 mm	0.26 mm	0.26 mm	0.28 mm	0.28 mm	0.28 mm	0.28 mm
Membrane Material	Cuprophane	Cuprophane	Cuprophane	Cuprophane	Cuprophane	Cuprophane	Polyestersulfone (PES)	Polyestersulfone (PES)	Polyestersulfone (PES)	Polyestersulfone (PES)	Polyestersulfone (PES)	Polyestersulfone (PES)
Molecular Weight Cut-off	6 kD	6 kD	6 kD	6 kD	6 kD	6 kD	55 kD	55 kD	500 kD	500 kD	2 MDa	2 MDa
Shaft Diameter	0.38 mm	0.38 mm	0.38 mm	0.38 mm	0.38 mm	0.38 mm	0.40 mm	0.40 mm	0.40 mm	0.40 mm	0.40 mm	0.40 mm
Shaft Length Metric	7 mm	7 mm	7 mm	7 mm	7 mm	7 mm	7 mm	7 mm	14 mm	14 mm	14 mm	14 mm
Inlet Volume	negligible	negligible	negligible	negligible	negligible	negligible	0.06 µL	0.06 µL	0.06 µL	0.06 µL	0.06 µL	0.06 µL
Outlet Volume	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL	0.3 µL
200 mm Inlet tubing (blue)	3.5 µL	3.5 µL	3.5 µL	3.5 µL	3.5 µL	3.5 µL	3.6 µL	3.6 µL	3.5 µL	3.5 µL	3.5 µL	3.5 µL
200 mm Outlet tubing (transp.)	3.5 µL	3.5 µL	3.5 µL	3.5 µL	3.5 µL	3.5 µL	3.6 µL	3.6 µL	3.5 µL	3.5 µL	3.5 µL	3.5 µL
Model	Standard	Standard	Metal Free	Metal Free	β-Irradiated	β-Irradiated	Standard	Standard	Standard	Standard	Standard	Standard

Journal Articles

Yau JL, Noble J, Kenyon CJ, Ludwig M, Seckl JR. (2015 ) Diurnal and stress-induced intra-hippocampal corticosterone rise attenuated in 11β-HSD1-deficient mice: a microdialysis study in young and aged mice. Eur J Neurosci.

Pawlisch BA, Remage-Healey L. (2015 ) Neuroestrogen signaling in the songbird auditory cortex propagates into a sensorimotor network via an 'interface'nucleus Neuroscience.

Dall, C. et al., 2017. Muscarinic receptor M4 positive allosteric modulators attenuate central effects of
cocaine. Drug and Alcohol Dependence, 176, pp.154–161.

Chen, X. et al., 2017. Influence of peptide transporter 2 (PEPT2) on the distribution of cefadroxil in mouse
brain: A microdialysis study. Biochemical Pharmacology, 131, pp.89–97.

Bank, J.H.H. et al., 2017. Gene expression analysis and microdialysis suggest hypothalamic triiodothyronine
(T3) gates daily torpor in Djungarian hamsters (Phodopus sungorus). Journal of Comparative Physiology B,
pp.1–12.

Ramírez-Jarquín, U.N. et al., 2017. Chronic infusion of SOD1G93A astrocyte-secreted factors induces spinal
motoneuron degeneration and neuromuscular dysfunction in healthy rats. Journal of Cellular Physiology,
p.n/a-n/a.

Yoshimoto, K. et al., 2017. Enhanced alcohol-drinking behavior associated with active cholinergic and
serotoninergic neurons in the lateral hypothalamus and amygdala. Pharmacology Biochemistry and
Behavior, 153, pp.1–11.

Ramírez-Jarquín, U.N. & Tapia, R., 2017. Chronic GABAergic blockade in the spinal cord in vivo induces
motor alterations and neurodegeneration. Neuropharmacology, 117, pp.85–92.

Moreno-Castilla, P. et al., 2017. Hippocampal release of dopamine and norepinephrine encodes novel
contextual information. Hippocampus, 27(5), pp.547–557.

Rapanelli, M. et al., 2017. Histamine H3R receptor activation in the do rsal striatum triggers stereotypies in a
mouse model of tic disorders. Translational Psychiatry, 7(1), p.e1013.

Pham, T.H. et al., 2017. Ketamine treatment involves medial prefrontal cortex serotonin to induce a rapid
antidepressant-like activity in BALB/cJ mice. Neuropharmacology, 112, Part A, pp.198–209.

Callan, S.P. et al., 2017. Toluene’s effects on activity and extracellular dopamine in the mouse are altered by
GABAA antagonism. Neuroscience Letters, 647, pp.67–71.

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