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Biosensis

Biosensis are a team of scientists and business people dedicated to the support of researchers in academia and industry. The team has had many years experience both in basic and applied research as well as in the commercialisation of reagent and diagnostic antibodies. Biosensis specialise in Neuroscience and Autophagy and have a growing range of antibodies in the field of Alzheimer`s and Parkinson's disease.

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Keeping Excitatory Neurons on a Short ‘Leash’

Inhibitory GABAergic interneurons are crucial elements of neuronal circuits, in particular for their role in ‘taming’ excitatory glutamatergic neurons. Interneurons represent a mixture of diverse neuronal sub-populations, and thus, antibodies to specific cell markers are important to differentiate interneuron cell types. An excellent review by Wamsley and Fishell (2017), discusses interneuron diversity and two interneuron markers, parvalbumin and calretinin, among many others.

Inhibitory GABAergic interneurons are crucial elements of neuronal circuits, in particular for their role in ‘taming’ excitatory glutamatergic neurons. Interneurons represent a mixture of diverse neuronal sub-populations, and thus, antibodies to specific cell markers are important to differentiate interneuron cell types. An excellent review by Wamsley and Fishell (2017), discusses interneuron diversity and two interneuron markers, parvalbumin and calretinin, among many others.

Biosensis’ NEW mouse, rabbit and chicken antibodies to human calretinin (M-1799-100, R-1800-50, C-1801-50) and parvalbumin (M-1813-100, C-1814-50) are high-quality research reagents for immunohistochemical and western blotting studies to identify the physiological role of neuronal sub-populations.

Left: Rat cerebellum section stained with mouse anti-parvalbumin (M-1813-100, green) and chicken anti-calbindin (C-1798-50, red) by Immunohistochemistry. Blue: DAPI nuclear stain. Most Purkinje cells strongly express both parvalbumin and calbindin and thus appear yellow. Basket, stellate and Golgi cells express parvalbumin alone, and thus appear green. Right: Detection of calretinin (29 kDa) by Western Blotting with rabbit anti-calretinin (R-1800-50) in (2) rat brain, (3) rat spinal cord, (4) mouse brain, (5) mouse spinal cord, and (6) cow spinal cord homogenates.