Product Catalogue

CMA 7 Microdialysis Probes

Art.-Nr. CMA 7 Microdialysis Probes
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Artikelbeschreibung

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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