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Cd8 pecy7 or apc

Manufactured by Thermo Fisher Scientific
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The CD8/PeCy7 or APC is a laboratory instrument designed for the detection and analysis of CD8+ T cells. It utilizes fluorescent labeling to identify and quantify the presence of these cells in biological samples. The core function of this product is to provide researchers with a reliable and accurate method for assessing CD8+ T cell populations.

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Lab products found in correlation

Canto 2, by BD (2 mentions) Annexin 5 apc, by Thermo Fisher Scientific (2 mentions) Cd19 apc, by Thermo Fisher Scientific (2 mentions) Streptavidin pecy5, by BD (2 mentions) Cd117 pecy7, by Thermo Fisher Scientific (2 mentions) Cd4 pe or pb, by Thermo Fisher Scientific (2 mentions) Cd279 bv421, by Thermo Fisher Scientific (2 mentions) Cd117 apccy7, by Thermo Fisher Scientific (2 mentions) Gr 1 pe, by Thermo Fisher Scientific (2 mentions) Apc brdu flow kit, by BD (2 mentions) Cd11b percp cy5, by Thermo Fisher Scientific (2 mentions) Cd45.1 pe, by Thermo Fisher Scientific (2 mentions) Moflow, by Beckman Coulter (2 mentions) B220 apc cy7, by Thermo Fisher Scientific (2 mentions) Tcrβ pe, by Thermo Fisher Scientific (2 mentions) Ki67 pe, by Thermo Fisher Scientific (2 mentions) Sca 1 apc, by Thermo Fisher Scientific (2 mentions) Cd45.2 apc, by Thermo Fisher Scientific (2 mentions)

Close spelling variants of this product

CD8-APC (44 citations)

2 protocols using cd8 pecy7 or apc

1

Multi-lineage Hematopoietic Cell Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total white blood cells from hematopoietic organs were stained in PBS supplemented with 2% FBS with fluorochrome-conjugated mouse antibodies against specific hematopoietic lineage markers. For the analysis of transplant-receiving mice, WBM was stained with fluorochrome-conjugated mouse antibodies to discriminate cells derived from competitors and donors (CD45.1+ and CD45.2+ respectively) and GFP expression was used to precisely define donor-derived cells (GFP+ CD45.2+). Fluorochrome-conjugated mouse antibodies were obtained from Becton Dickinson (Streptavidin/PeCy5, CD117/PeCy7, CD45.1/PE, CD4/PE or PB, CD8/PeCy7 or APC, CD19/APC, B220/APCCy7, TCRβ/PE, CD279/BV421, CD11b/PerCP-Cy5.5, Annexin V/APC, Ki67/PE) and eBiosciences (CD117/APCCy7, Sca-1/APC, CD45.2/APC, Gr1/PE). Hoescht 33342 was obtained from Invitrogen. APC BrdU Flow kit (Becton Dickinson) was used according to the manufacturer’s instruction. Cell sorting was performed either on a MoFlow (Beckman Coulter) or Influx (Becton Dickinson) cell sorter and analysis on a Canto II (Becton Dickinson). FACS data were analyzed by FlowJo Software (v8.8.7).
Scourzic L., Couronné L., Pedersen M.T., Della Valle V., Diop M., Mylonas E., Calvo J., Mouly E., Lopez C.K., Martin N., Fontenay M., Bender A., Guibert S., Dubreuil P., Dessen P., Droin N., Pflumio F., Weber M., Gaulard P., Helin K., Mercher T, & Bernard O.A. (2016). DNMT3AR882H mutant and Tet2 inactivation cooperate in the deregulation of DNA methylation control to induce lymphoid malignancies in mice. Leukemia, 30(6), 1388-1398.
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2

Multi-lineage Hematopoietic Cell Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total white blood cells from hematopoietic organs were stained in PBS supplemented with 2% FBS with fluorochrome-conjugated mouse antibodies against specific hematopoietic lineage markers. For the analysis of transplant-receiving mice, WBM was stained with fluorochrome-conjugated mouse antibodies to discriminate cells derived from competitors and donors (CD45.1+ and CD45.2+ respectively) and GFP expression was used to precisely define donor-derived cells (GFP+ CD45.2+). Fluorochrome-conjugated mouse antibodies were obtained from Becton Dickinson (Streptavidin/PeCy5, CD117/PeCy7, CD45.1/PE, CD4/PE or PB, CD8/PeCy7 or APC, CD19/APC, B220/APCCy7, TCRβ/PE, CD279/BV421, CD11b/PerCP-Cy5.5, Annexin V/APC, Ki67/PE) and eBiosciences (CD117/APCCy7, Sca-1/APC, CD45.2/APC, Gr1/PE). Hoescht 33342 was obtained from Invitrogen. APC BrdU Flow kit (Becton Dickinson) was used according to the manufacturer’s instruction. Cell sorting was performed either on a MoFlow (Beckman Coulter) or Influx (Becton Dickinson) cell sorter and analysis on a Canto II (Becton Dickinson). FACS data were analyzed by FlowJo Software (v8.8.7).
Scourzic L., Couronné L., Pedersen M.T., Della Valle V., Diop M., Mylonas E., Calvo J., Mouly E., Lopez C.K., Martin N., Fontenay M., Bender A., Guibert S., Dubreuil P., Dessen P., Droin N., Pflumio F., Weber M., Gaulard P., Helin K., Mercher T, & Bernard O.A. (2016). DNMT3AR882H mutant and Tet2 inactivation cooperate in the deregulation of DNA methylation control to induce lymphoid malignancies in mice. Leukemia, 30(6), 1388-1398.
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