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Mouse trf1

Manufactured by Thermo Fisher Scientific

Mouse TRF1 is a laboratory product used for the detection and analysis of the TRF1 protein in mouse samples. TRF1 is a key component of the telomere complex and plays a crucial role in telomere length regulation. This product provides researchers with a tool to study the expression and function of TRF1 in mouse models.

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3 protocols using mouse trf1

1

Immunofluorescence Staining of Naïve CD4 T Cells

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Naïve CD4 T cells were isolated and cultured as described above, followed by immunofluorescence staining using a method described previously6 (link). Rabbit anti-53BP1 (Cell Signaling) and mouse TRF1 (Thermo Fisher) were used as primary antibodies and anti-rabbit IgG-Alexa Fluor 488 and anti-mouse IgG- Alexa Fluor 555 (Invitrogen) were used as secondary antibodies. Then, cells were washed and mounted with DAPI Fluoromount-G (SouthernBiotech, Birmingham, AL). Images were acquired with a confocal laser-scanning inverted microscope (Leica Confocal, Model TCS sp8, Germany).
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2

Quantifying Telomere Dynamics in T Cells

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CD4 T cells were isolated and cultured as described above, followed by immunofluorescence staining using a method described previously6 . The primary antibodies included Rabbit anti-53BP1, and mouse TRF1 (Thermo Fisher). The secondary antibodies included anti-rabbit IgG-Alexa Fluor 488 and anti-mouse IgG-Alexa Fluor 555 (Invitrogen). We also used Tel-C (TAACCC)-FITC probe for telomere staining. The cells were washed and mounted with DAPI Fluoromount-G (SouthernBiotech, Birmingham, AL). Images were acquired with a confocal laser-scanning inverted microscope (Leica Confocal, Model TCS sp8, Germany).
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3

Visualizing DNA Repair Foci in CD4 T Cells

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CD4 T cells were isolated and treated as described above, followed by immunofluorescence staining using a method described previously [26 (link)]. Rabbit anti-53BP1, anti-Ku70, anti-RAD51 or anti-Top1cc (Cell Signaling) and mouse TRF1 (Thermo Fisher) were used as primary antibodies and anti-rabbit IgG-Alexa Fluor 488 and anti-mouse IgG-Alexa Fluor 555 (Invitrogen) were used as secondary antibodies. The cells were washed and mounted with DAPI Fluoromount-G (SouthernBiotech, Birmingham, AL). Images were acquired with a confocal laser-scanning inverted microscope (Leica Confocal, Model TCS sp8, Germany).
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