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Total tau

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Total-tau is a laboratory equipment product designed to measure the concentration of the tau protein in biological samples. Tau protein is a biomarker associated with various neurological conditions. The Total-tau product provides a tool for researchers and clinicians to quantify tau levels, which can be useful for diagnostic and research purposes.

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Lab products found in correlation

Foxg1, by Santa Cruz Biotechnology (2 mentions) Bz 9000e fluorescence microscope, by Leica camera (2 mentions) Alexa fluor 594, by Thermo Fisher Scientific (2 mentions) Mab1637, by Merck Group (2 mentions) Ab5622, by Merck Group (2 mentions) Leica confocal imaging system, by Leica camera (2 mentions) Alexa fluor 488 conjugated igg, by Thermo Fisher Scientific (2 mentions) Nestin, by Merck Group (2 mentions) At180, by Thermo Fisher Scientific (2 mentions) Mab5326, by Merck Group (2 mentions) Cleaved caspase 3, by Cell Signaling Technology (2 mentions) Mrb 435p, by Fortrea (2 mentions) Epifluorescence microscope, by Keyence (2 mentions)

2 protocols using total tau

1

Immunostaining of Neural Progenitors and Neurons

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All neural progenitors, including MGE cells, and further differentiated cells, including MGE cell-derived GABAergic neurons, were fixed in 4% paraformaldehyde and stained with the following primary antibodies: nestin (MAB5326, EMD Millipore), Pax6 (Developmental Studies Hybridoma Bank), FoxG1 (sc-48788, Santa Cruz Biotechnology), MAP2 (MAB3418, AB5622, EMD Millipore), Tuj1 (MAB1637, EMD Millipore; MRB-435P, Covance), apoE (178479, Calbiochem), PHF1 (gift from Peter Davies), AT8 (MN1020, Thermo Fisher Scientific), AT180 (MN1040, Thermo Fisher Scientific), Tau5 (577801, EMD Millipore), total-tau (T6402, Sigma), NKX2.1 (sc-13040, Santa Cruz Biotechnology), GABA (A2052, Sigma), and cleaved Caspase-3 (D3E9, Cell Signaling Technology). The secondary antibodies were IgG-conjugated Alexa Fluor 488 or Alexa Fluor 594 (Life Technologies). Nuclei were stained with DAPI. Images were taken with a Leica epifluorescence microscope, a Keyence BZ-9000E fluorescence microscope, or a Leica confocal imaging system.
Wang C., Najm R., Xu Q., Jeong D.E., Walker D., Balestra M.E., Yoon S.Y., Yuan H., Li G., Miller Z.A., Miller B.L., Malloy M.J, & Huang Y. (2018). Gain of toxic Apolipoprotein E4 effects in Human iPSC-Derived Neurons Is Ameliorated by a Small-Molecule Structure Corrector. Nature medicine, 24(5), 647-657.
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2

Immunostaining of Neural Progenitors and Neurons

Check if the same lab product or an alternative is used in the 5 most similar protocols
All neural progenitors, including MGE cells, and further differentiated cells, including MGE cell-derived GABAergic neurons, were fixed in 4% paraformaldehyde and stained with the following primary antibodies: nestin (MAB5326, EMD Millipore), Pax6 (Developmental Studies Hybridoma Bank), FoxG1 (sc-48788, Santa Cruz Biotechnology), MAP2 (MAB3418, AB5622, EMD Millipore), Tuj1 (MAB1637, EMD Millipore; MRB-435P, Covance), apoE (178479, Calbiochem), PHF1 (gift from Peter Davies), AT8 (MN1020, Thermo Fisher Scientific), AT180 (MN1040, Thermo Fisher Scientific), Tau5 (577801, EMD Millipore), total-tau (T6402, Sigma), NKX2.1 (sc-13040, Santa Cruz Biotechnology), GABA (A2052, Sigma), and cleaved Caspase-3 (D3E9, Cell Signaling Technology). The secondary antibodies were IgG-conjugated Alexa Fluor 488 or Alexa Fluor 594 (Life Technologies). Nuclei were stained with DAPI. Images were taken with a Leica epifluorescence microscope, a Keyence BZ-9000E fluorescence microscope, or a Leica confocal imaging system.
Wang C., Najm R., Xu Q., Jeong D.E., Walker D., Balestra M.E., Yoon S.Y., Yuan H., Li G., Miller Z.A., Miller B.L., Malloy M.J, & Huang Y. (2018). Gain of toxic Apolipoprotein E4 effects in Human iPSC-Derived Neurons Is Ameliorated by a Small-Molecule Structure Corrector. Nature medicine, 24(5), 647-657.
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