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  • Lentiviral vector plasmid for overexpression of ATP10B (R153X)

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    Plasmid: Lentiviral vector plasmid for overexpression of ATP10B (R153X) validated for use in cell culture.

  • Lentiviral vector plasmid for overexpression of ATP10B (E210A)

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    Plasmid: Lentiviral vector plasmid for overexpression of ATP10B (E210A) validated for use in cell culture.

  • Lentiviral vector plasmid for overexpression of ATP10B (EmGFP)

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    Plasmid: Lentiviral vector plasmid for overexpression of ATP10B (EmGFP) validated for use in cell culture.

  • pAAV_Cbh_DIO_hTyrNull_HATag

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    Cre-dependent expression of a truncated human tyrosinase is inactive and does not lead to the accumulation of neuromelanin in catecholaminergic neurons (control virus). Strong expression of CbH promoter that is non-silencenable, HA tag for histological verification of expression.

  • pAAV_hSyn_GCaMP6m_sWPRE_spA_mDLX_nls_mRuby3_ssWPRE_spA

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    A viral construct designed to express GCaMP6m pan-neuronally and express a red fluorophore (mRuby) in the nucleus of cortical interneurons. This construct is ideal for dual-imaging experiments to capture activity of two neuronal populations and to identify interneurons with red fluorescence in parallel or post-mortem.

  • pAAV_Ef1a_DIO_MyrPalm_mScarlet_WT_IRES_mNeon_minBack

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    Bright green (mNeon) and red (mRuby) fluorescence proteins are expressed, with the former being cytoplasmic and the latter membrane-targeted. This expression is ideal for tracking long diffuse axons in cortical structures in vivo or for slice histology and cleared brain tissues post-mortem.

  • pAAV_EF1a_DIO_jGCaMP8f_nano_ribo_WPRE

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    This links GCaMP8f with a ribosome-tethered nanobody that restricts GCaMP to the soma of neurons. Particularly useful in very dense nuclei with strong neuropil, which can make post-hoc cell segmentation (i.e., independent component analysis (ICA) or constrained nonnegative matrix factorization (CMNF)) difficult.

  • pAAV_Ef1a_DIO_hTyrNull_HATag

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    Cre-dependent expression of a truncated human tyrosinase is inactive and does not lead to the accumulation of neuromelanin in catecholaminergic neurons (control virus). Strong expression of Ef1a promoter, HA tag for histological verification of expression.

  • pAAV_Ef1a_DIO_hTyrHA_minBack

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    Cre-dependent expression of human tyrosinase induces the formation of neuromelanin in catecholaminergic neurons. Expression under strong Ef1a promoter.

  • pAAV_Cbh_DIO_hTyr

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    Cre-dependent expression of human tyrosinase induces the formation of neuromelanin in catecholaminergic neurons. The CbH promoter is a strong, pan-neuronal, non-silencable promoter.

  • pAAV_CbH_SIO_SyGCaMP8s_p2a_mRuby

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    This construct links GCaMP8s to Synaptophysin and directs the fusion protein to presynaptic sites. It also produces a cytoplasmic red fluorescence protein (mRuby) via the self-splicing peptide 2A. It is mainly used to longitudinally image synaptic activity with 2-Photon at 980nm and visualize axons at 1080nm in vivo.

  • HEK293T SNCA-A53T-mRuby3 SNCA-A53T-mClover3

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    Cell Line: Transfected with two plasmids encoding mRuby3- and mClover3-tagged SNCA p.Ala53Thr expressed under the control of CMV promoters.

  • HEK293E_Ecto short VLDLR-C-tag

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing the ectodomain of VLDLR fused to a C-terminal C-tag (EPEA) under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu WT

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu TL4

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu TL3

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu TL2+3

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu TL1

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu DD3

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

  • HEK293E_Clu DD1

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    Cell Line: Transfected with the pB-T-PAF expression plasmid expressing CLU under the tet operator and the PB-RN reverse transactivator plasmid expressing the reverse tetracycline-controlled transactivator under the CMV promoter.

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