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Large Animal Stereotaxic Instruments
Large Animal Stereotaxic Instruments

Large Animal Stereotaxic Instruments

Vendor: RWD Life Science
Type: Animal Research Equipment
Large animal stereotaxic instrument is suitable for cats, dogs, monkeys, pigs, etc. It contains a two-dimensional manipulator (X, Z axis). The accuracy of th... ... Read More
Name
Price Unit
Quantity
68814 Stereotaxic for Large Animals Dual M
$8,170.00
68815 Stereotaxic for Large Animals SGL M Digital
$8,300.00
68816 Stereotaxic for Large Animals Dual M Digital
$12,080.00
68041 Cat/Monkey Adaptor
$310.00
68081 Dog/Monkey/Pig Adaptor
$940.00
68303 Cat/Monkey 18° Ear Bars
$200.00
68304 Cat/Monkey 45° Ear Bars
$200.00
68201 Standard Probe Holder-Corner clamping range 0.3-1.5mm.
$128.80 $161.00
68217 Cannula Holder clamping diameter 3.5mm The clamping part is made of plastic.
$130.00
68205 Cannula Holder clamping diameter 3.5mm The clamping part is made of metal.
$130.00
68214 Ceramic Ferrule Holder clamping diameter 1.25mm
$170.00
68215 Ceramic Ferrule Holder clamping diameter 2.5mm
$170.00
68206 General Probe Holder clamping range: 3-12mm
$130.00
68218 Syringe Holder the syringe barrel clamping range is 6mm-12mm and the syringe needle clamping range is 0.3mm-1.5mm
$200.00
68605 Microdrill Holder clamping diameter: 14.5mm
$104.00 $130.00

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Delivery timelines will be provided with your quote

Delivery timelines will be provided with your quote

Standard lead time varies by product availability (in-stock items usually 1–3 business days, custom/backordered items 7–21 business days).

90-day return policy

90-day return policy

Eligible items may be returned within 90 days after delivery, subject to our Return Policy.

Notice

Notice

Final delivery schedules and pricing are subject to confirmation in your official quotation. Customs policies may also impact the total cost. Contact us for your best quote.

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Overview
Feature
Applications
Specifications
Order Information
Literature
Customer Review

overview

Large animal stereotaxic instrument is suitable for cats, dogs, monkeys, pigs, etc. It contains a two-dimensional manipulator (X, Z axis). The accuracy of the non-digital model is 100 μm, and the accuracy of the digital model is 10 μm. Two kinds of adaptors are optional, the 68081 monkey adaptor is generally suitable for large animals of 10-30kg, and the 68041 is generally suitable for large animals below 10kg.

Features & Benefits

High Precision Positioning

Available in both mechanical and digital versions. The non-digital model provides 100 μm accuracy, while the digital model achieves up to 10 μm positioning accuracy to meet advanced research requirements.

Two-Dimensional Precision Manipulator

Equipped with a smooth and stable X–Z axis manipulator for accurate coordinate adjustment and reliable targeting during procedures.

Flexible Configuration Options

Choose between digital and non-digital configurations based on experimental precision needs and budget considerations.

Adaptable for Different Animal Sizes

Two optional adaptors are available: Model 68081 for animals weighing 10–30 kg, and Model 68041 for animals below 10 kg.

Stable Structural Design

Engineered specifically for large animals to ensure secure fixation and consistent experimental stability throughout surgical and research procedures.

Applications

Neuroscience Research

Brain Localization and Targeting Procedures

Stereotaxic Surgery

Preclinical Studies

Electrophysiology and Microinjection Experiments

Specifications

Parameter Description
Positioning Accuracy (Digital) 10 μm
Positioning Accuracy (Non-Digital) 100 μm
Manipulator Axes X, Z
Compatible Animals Cats, Dogs, Monkeys, Pigs
Adaptor Model 68081 Suitable for 10–30 kg animals
Adaptor Model 68041 Suitable for animals below 10 kg
Configuration Options Digital / Non-digital

Order Information

Stereotaxic Host (Without Accessories)

Model Product Description Remark
68813 Stereotaxic for Large Animals, SGL M. Standard configuration, non-digital display model (accuracy 100 μm), including 68868N base, 68941 2-axis manipulator-left, without adaptor, ear bars and holder.
68814 Stereotaxic for Large Animals, Dual M. Standard configuration, non-digital display model (accuracy 100 μm), including 68868N base, 68941 2-axis manipulator-left, 68942 2-axis manipulator-right, without adaptor, ear bars and holder.
68815 Stereotaxic for Large Animals, SGL M, Digital Standard configuration, digital display model (accuracy 10 μm), including 68868N base, 68944 2-axis digital manipulator-left, without adaptor, ear bars and holder.
68816 Stereotaxic for Large Animals, Dual M, Digital Standard configuration, digital display model (accuracy 10 μm), including 68868N base, 68944 2-axis digital manipulator-left, 68945 2-axis digital manipulator-right, without adaptor, ear bars and holder.

Required Accessories (Optional)

Model Product Description Remark
68041 Cat/Monkey Adaptor Suitable for animals under 10 kg (cats, dogs, monkeys, etc.). Please confirm head width, distance from nose to eyes, mouth width and other details before purchasing.
68081 Dog/Monkey/Pig Adaptor Suitable for 10–30 kg animals (cats, dogs, monkeys, etc.). Please confirm head width, distance from nose to eyes, mouth width and other details before purchasing.
68303 Cat/Monkey 18° Ear Bars -
68304 Cat/Monkey 45° Ear Bars -
68201 Standard Probe Holder – Corner (0.3–1.5 mm) -
68217 Cannula Holder (3.5 mm) Clamping part made of plastic
68205 Cannula Holder (3.5 mm) Clamping part made of metal
68214 Ceramic Ferrule Holder (1.25 mm) -
68215 Ceramic Ferrule Holder (2.5 mm) -
68206 General Probe Holder (3–12 mm) -
68218 Syringe Holder (barrel: 6–12 mm; needle: 0.3–1.5 mm) -
68605 Microdrill Holder (14.5 mm) Suitable for 78001 microdrill

literature

Diao, Y., Cui, L., Chen, Y., Burbridge, T. J., Han, W., Wirth, B., … & Zhang, J. (2018). Reciprocal connections between cortex and thalamus contribute to retinal axon targeting to dorsal lateral geniculate nucleus. Cerebral Cortex, 28(4), 1168-1182.

Fan, X. C., Fu, S., Liu, F. Y., Cui, S., Yi, M., & Wan, Y. (2018). Hypersensitivity of prelimbic cortex neurons contributes to aggravated nociceptive responses in rats with experience of chronic inflammatory pain. Frontiers in molecular neuroscience, 11, 85.

Liu, Y., Lai, S., Ma, W., Ke, W., Zhang, C., Liu, S., … & Shu, Y. (2017). CDYL suppresses epileptogenesis in mice through repression of axonal Nav1. 6 sodium channel expression. Nature communications, 8(1), 1-17.

Tang, Y., Lin, Y. H., Ni, H. Y., Dong, J., Yuan, H. J., Zhang, Y., … & Chang, L. (2017). Inhibiting Histone Deacetylase 2 (HDAC 2) Promotes Functional Recovery From Stroke. Journal of the American Heart Association, 6(10), e007236.

Huang, L., Yuan, T., Tan, M., Xi, Y., Hu, Y., Tao, Q., … & Luo, M. (2017). A retinoraphe projection regulates serotonergic activity and looming-evoked defensive behaviour. Nature communications, 8(1), 1-13.

Zhu, M., Li, H., Gyanwali, B., He, G., Qi, C., Yang, X., … & Tang, A. (2017). Auditory brainstem responses after electrolytic lesions in bilateral subdivisions of the medial geniculate body of tree shrews. Neurological Sciences, 38(9), 1617-1628.

Lei, Z., Wang, D., Chen, N., Ma, K., Lu, W., Song, Z., … & Wang, J. H. (2017). Synapse innervation and associative memory cell are recruited for integrative storage of whisker and odor signals in the barrel cortex through miRNA-mediated processes. Frontiers in cellular neuroscience, 11, 316.

Zhou, H., Xiong, G. J., Jing, L., Song, N. N., Pu, D. L., Tang, X., … & Richter-Levin, G. (2017). The interhemispheric CA1 circuit governs rapid generalisation but not fear memory. Nature communications, 8(1), 1-10.

Zhang, J., Liu, H., Du, X., Guo, Y., Chen, X., Wang, S., … & Zhang, W. (2017). Increasing of blood-brain tumor barrier permeability through transcellular and paracellular pathways by microbubble-enhanced diagnostic ultrasound in a C6 glioma model. Frontiers in neuroscience, 11, 86.

Li, G. F., Zhao, H. X., Zhou, H., Yan, F., Wang, J. Y., Xu, C. X., … & Zhang, H. L. (2016). Improved anatomical specificity of non-invasive neuro-stimulation by high frequency (5 MHz) ultrasound. Scientific reports, 6(1), 1-11.

Liu, M. G., Li, H. S., Li, W. G., Wu, Y. J., Deng, S. N., Huang, C., … & Xu, T. L. (2016). Acid-sensing ion channel 1a contributes to hippocampal LTP inducibility through multiple mechanisms. Scientific reports, 6, 23350.

Zhao, Baisong, et al. “Hyperbaric oxygen pretreatment improves cognition and reduces hippocampal damage via p38 mitogen-activated protein kinase in a rat model.” Yonsei medical journal 58.1 (2017): 131-138.

Zhao, Yunan, et al. “Decreased glycogen content might contribute to chronic stress-induced atrophy of hippocampal astrocyte volume and depression-like behavior in rats.” Scientific reports 7 (2017): 43192.

Espinosa, P., Silva, R. A., Sanguinetti, N. K., Venegas, F. C., Riquelme, R., González, L. F., … & Sotomayor-Zárate, R. (2016). Programming of dopaminergic neurons by neonatal sex hormone exposure: effects on dopamine content and tyrosine hydroxylase expression in adult male rats. Neural plasticity, 2016.

Li, Wei-Guang, et al. “ASIC1a regulates insular long-term depression and is required for the extinction of conditioned taste aversion.” Nature communications 7.1 (2016): 1-15.

Wang, G. Q., Cen, C., Li, C., Cao, S., Wang, N., Zhou, Z., … & Wang, J. (2015). Deactivation of excitatory neurons in the prelimbic cortex via Cdk5 promotes pain sensation and anxiety. Nature communications, 6(1), 1-16.