Viewing entries tagged
posterior tuberculum

Tyrosine Hydroxylase

Tyrosine Hydroxylase

Tyrosine Hydroxylase

ABOUT THIS ANTIBODY

Tyrosine Hydroxylase is an enzyme that catalyses the convertion of L-tyrosine to L-3,4-dihydroxyphenylalanine(L-DOPA) which is the precursor for the neurotransmitter dopamine. anti-TH labels dopaminergic neurons in the olfactory bulb, subpallium, preotic area, posterior tuberculum and locus coeruleus.

Rabbit polyclonal anti-TH (Chemicon/Millipore , Cat#AB152, dilution 1:1000)

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External Links:

 ZFIN


LABELS THESE BRAIN STRUCTURES:

 olfactory bulb, preoptic area, posterior tuberculum.


KEY PUBLICATIONS

 Yamamoto, K., Ruuskanen, J.O., Wullimann, M.F., and Vernier, P. (2010)
Two tyrosine hydroxylase genes in vertebrates: New dopaminergic territories revealed in the zebrafish brain. Molecular and Cellular Neuroscience. 43(4):394-402.

Yamamoto, K., Ruuskanen, J.O., Wullimann, M.F., and Vernier, P. (2011)
Differential expression of dopaminergic cell markers in the adult zebrafish forebrain.
The Journal of comparative neurology. 519(3):576-598.

Xi, Y., Yu, M., Godoy, R., Hatch, G., Poitras, L., and Ekker, M. (2011)
Transgenic zebrafish expressing green fluorescent protein in dopaminergic neurons of the ventral diencephalon.
Developmental dynamics. 240(11):2539-47.

5-HT (serotonin)

5-HT (serotonin)

5-HT(serotonin)

ABOUT THIS ANTIBODY

5-HT labels serotinergic neurons in the pineal organ, pretectum, posterior tuberculum, hypothalamus and superior and inferior raphe.

Rat monoclonal anti-5-HT (IgG) (Chemicon/Millipore, Cat#MAB352, dilution 1:500)

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External Links:

 ZFIN


LABELS THESE BRAIN STRUCTURES:

 pineal organ, pretectum, posterior tuberculum, hypothalamus, superior raphe, inferior raphe.


KEY PUBLICATIONS

Lillesaar.
The serotonergic system in fish.
J Chem Neuroanat (2011) vol. 41 (4) pp. 294-308

Gaspar & Lillesaar.
Probing the diversity of serotonin neurons.
Philos Trans R Soc Lond B Biol Sci. 2012 Sep 5;367(1601):2382-94. doi: 10.1098/rstb.2011.0378.

Lillesaar et al.
Axonal projections originating from raphe serotonergic neurons in the developing and adult zebrafish, Danio rerio, using transgenics to visualize raphe-specific pet1 expression.
J Comp Neurol. 2009 Jan 10;512(2):158-82. doi: 10.1002/cne.21887.

Panula et al.
Modulatory neurotransmitter systems and behavior: towards zebrafish models of neurodegenerative diseases.
Zebrafish (2006) vol. 3 (2) pp. 235-47

McLean and Fetcho.
Ontogeny and innervation patterns of dopaminergic, noradrenergic, and serotonergic neurons in larval zebrafish.
J. Comp. Neurol. (2004) vol. 480 (1) pp. 38-56

Wen et al.
Visualization of monoaminergic neurons and neurotoxicity of MPTP in live transgenic zebrafish. Developmental Biology (2008) vol. 314 (1) pp. 84-92 

Calretinin

Calretinin

Rabbit anti-calretinin

ABOUT THIS ANTIBODY

anti-calretinin labels neurons expressing the calcium binding protein calretinin.

Calcium-binding preoteins contribute to calcium homeostasis by buffering intercellular calcium. This antibody labels distinct groups of neurons in the central and peripheral nervous system.
 

Rabbit Polyclonal anti-calretinin (Swant, Cat#CR7697, dilution 1:1000)

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EXTERNAL LINKS:

 ZFIN:https://zfin.org/ZDB-ATB-160726-1
Swant: https://www.swant.com/pdfs/Rabbit_anti_calretinin_7697.pdf


LABELS THESE BRAIN STRUCTURES:

olfactory epithelium, olfactory glomeruli, dorsal telencephalon, ventral telencephalon, entopeduncular nucleus, preoptic area, preglomerular complex, mammillary body, hypothalamus (inferior lobe), torus lateralis, posterior tuberculum, thalamus(anterior thalamic nucleus), pretectum (parvocellular superficial pretectal nucleus), nucleus of the medial longitudinal fascicle. 


KEY PUBLICATIONS

Castro A1, Becerra M, Manso MJ, Anadón R.
Calretinin immunoreactivity in the brain of the zebrafish, Danio rerio: distribution and comparison with some neuropeptides and neurotransmitter-synthesizing enzymes. I. Olfactory organ and forebrain.
J Comp Neurol. 2006 Jan 20;494(3):435-59.

Beretta, C.A., Dross, N., Guglielmi, L., Bankhead, P., Soulika, M., Gutierrez-Triana, J.A., Paolini, A., Poggi, L., Falk, J., Ryu, S., Kapsimali, M., Engel, U., Carl, M. (2017)
Early Commissural Diencephalic Neurons Control Habenular Axon Extension and Targeting.
Current biology : CB. 27(2):270–278.

Turner, K.J., Hawkins, T.A., Yáñez, J., Anadón, R., Wilson, S.W., Folgueira, M. (2016)
Afferent Connectivity of the Zebrafish Habenulae.
Frontiers in neural circuits 10:30. https://doi.org/10.3389/fncir.2016.00030