Herpes Simplex Virus (HSV) for Neuronal Tracing

Herpes Simplex Virus (HSV) for Neuronal Tracing

Catalog Number:
CFA1552398BRA
Mfr. No.:
H01001/2/3; H03001/2
Price:
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      • Overview
        • Herpes simplex virus (HSV), based on the H129 strain, has been widely used as an anterograde tracer. After adding the modified HSV with fluorescent protein, it can be used not only to efficiently label the connections between different brain regions, but also can label the connections between peripheral and central.

          Thymidine nucleotide kinase (TK) is an essential component for HSV replication after infection of nerve cells. In the presence of TK, HSV can replicate and express the target gene in the cell, and its progeny virus will transport to the synapse, and then crosses the synapse into the downstream neuron, so as to realize multisynaptic tracing. When removed TK (TK-deleted), HSV-ΔTK can infect neurons, but can't replicate. We know that only viruses that can replicate have the ability to cross synapses, so HSV-ΔTK can't cross the synapses. However, if we provide AAV virus as a helper to express TK protein fist, the HSV-ΔTK can realize anterograde monosynaptic tracing.

          Advantages
          · Fast and high efficiency
          · Strong background in neuronal tracing tool
          · Hypotoxicity and strong signal
          · The most competitive price

          Please contact us at for specific academic pricing.

          Background

          The neuronal connectivity by different synapses forms the brain's complex activities. So developing the technology to dissect the brain circuits became urgent in neuroscience to understand the brain functions. Currently, techniques for studying brain circuits include conventional tracers and recombinant viral vectors. The conventional tracers like CTB, HRP, PHA-L, BDAs and so on, but they have some disadvantages, such as:
          1) Cell specificity cannot be achieved.
          2) Efficiency is not stable.
          3) The circuits of the neurons at multiple step of synaptic connections cannot be realized.

          However, due to the ability to efficiently enter cells and deliver a variety of gene, genetically engineered recombinant viral vectors emerged as powerful tools for visualizing neural connectivity. The commonly used neurotropic virus, such as HSV (Herpes simplex virus type 1), VSV (Vesicular stomatitis virus), PRV (pseudorabies virus) and RABV (rabies virus) can cross synapse from one cell to another, if we provide the protein that used for replicate. In addition, there are also SFV (mark the fine morphology of in-situ neurons) and AAV viruses(as a helper virus to express exogenous genes or as a monosynaptic tracer with serotypes 1) that are used for neuronal tracing.

      • Properties
        • Other Properties
          Name: HSV-hUbC-eGFP
          Description: Labeled by eGFP with hUbC promoter.
          Product Type: Herpes simplex virus (HSV)
          Size: 50ul
          Titer: ≥2.00E+09 PFU/mL

          Name: HSV-tdTomato
          Description: Labeled by tdTomato
          Product Type: Herpes simplex virus (HSV)
          Size: 50ul
          Titer: ≥2.00E+09 PFU/mL

          Name: HSV-LSL-tdtomato-2a-TK(H356)
          Description: Labeled by eGFP.
          Product Type: Herpes simplex virus (HSV)
          Size: 50ul
          Titer: ≥2.00E+09 PFU/mL

          Name: HSV-ΔTK-hUbC-tdTomato
          Description: TK gene was completely removed (TK-deleted) and labeled by tdTomato.
          Product Type: Herpes simplex virus (HSV)
          Size: 50ul
          Titer: ≥2.00E+09 PFU/mL

          Name: HSV-ΔTK-LSL-tdTomato(H361)
          Description: Cre dependent, TK-deleted and labeled by tdTomato.
          Product Type: Herpes simplex virus (HSV)
          Size: 50ul
          Titer: ≥2.00E+09 PFU/mL
          Storage
          Should be stored at -80°C
      • Applications
        • Application Description
          · Multisynaptic tracing from the brain center to peripheral, or the lower to the higher brain region.
          · Tracking peripheral organs' connections to the central nervous system
          · Tracking the neural networks in disease or injury model.
          · Changes in neural networks during neural development.
      • Reference

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