Anti-Transferrin Receptor antibody [13E4]
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(13 제품이 사용된 논문 )
- Flow Cyt
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Flow Cytometry - Anti-Transferrin Receptor antibody [13E4] (AB38171)
Overlay histogram showing Jurkat cells stained with ab38171 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab38171, 0.5μg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line). Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in Jurkat cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
- ICC/IF
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Immunocytochemistry/ Immunofluorescence - Anti-Transferrin Receptor antibody [13E4] (AB38171)
ICC/IF image of ab38171 stained DU145 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab38171 at 5μg/ml overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti- mouse (ab96879) IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.
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This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TfR plays a critical role in iron homeostasis by mediating the internalization of transferrin and release of iron in the endosomes. It operates as part of the transferrin-transferrin receptor complex facilitating iron assimilation necessary for DNA synthesis and cell growth. Iron release involves acidifying endosomes allowing transferrin to bind with specific cellular receptors including alternate forms like beta 2 transferrin. The process subsequently contributes to erythropoiesis and various metabolic processes by regulating essential cellular iron levels.
Pathways
The transferrin receptor is central to iron metabolism and the receptor-mediated endocytosis pathway. It tightly interacts with transferrin and intracellular pathways process the iron released from transferrin within endosomes. The receptor's role in this pathway involves a dynamic with other proteins such as HFE and hepcidin. These interactions help control systemic iron levels linking closely to the maintenance of erythroid cell health and proliferation.
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제품이 사용된 논문 (13)
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The Journal of cell biology 223: PubMed38048228
2023
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Journal of structural biology: X 6:100056 PubMed34977554
2022
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American journal of cancer research 11:691-711 PubMed33791148
2021
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Molecules (Basel, Switzerland) 25: PubMed33348564
2020
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Cellular microbiology 23:e13270 PubMed32981231
2020
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Nature communications 10:2621 PubMed31197168
2019
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The Journal of cell biology 217:2549-2564 PubMed29891722
2018
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Scientific reports 8:8867 PubMed29891921
2018
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Nature communications 6:6289 PubMed25662504
2015
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Neurourology and urodynamics 35:382-9 PubMed25597596
2015
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