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mouse anti fmr1  (Developmental Studies Hybridoma Bank)
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Developmental Studies Hybridoma Bank mouse anti fmr1
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mouse antibody to fmr1  (Developmental Studies Hybridoma Bank)
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(A–G’) Co-localization analysis of Toll and subcellular compartment markers in Drosophila S2 cells. Toll-1::Venus was expressed by co-transfection of pActin-GAL4 and p20×UAS-Toll-1::Venus plasmids, followed by immunostaining to assess co-localization. (A and A’) Toll-1::Venus anti-Rab5 labeling. (B and B’) Toll-1::Venus anti-Rab7 labeling. (C and C’) Toll-1::Venus anti-Rab8 labeling. (D and D’) Toll-1::Venus anti-Atg8 labeling. (E and E’) Toll-1::Venus anti-Kdel labeling. (F and F’) Toll-1::Venus anti-Lamp1 labeling. (G and G’) Toll-1::Venus <t>anti-Fmr1</t> labeling. (H) Quantification of co-localization using Pearson’s correlation coefficients between Toll-1::Venus and various organelle markers: stress granules (Fmr1), lysosomes (Lamp1), endoplasmic reticulum (Kdel), autophagosomes (Atg8), early endosomes (Rab5), secretory vesicles (Rab8), and late endosomes (Rab7).
Mouse Antibody To Fmr1, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ab 568800 rabbit anti ha proteintech 51064 2 ap ab 11042321 mouse anti ha sigma aldrich h9658 100ul ab 260092 mouse anti drosophila fmr1  (Proteintech)
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(A–G’) Co-localization analysis of Toll and subcellular compartment markers in Drosophila S2 cells. Toll-1::Venus was expressed by co-transfection of pActin-GAL4 and p20×UAS-Toll-1::Venus plasmids, followed by immunostaining to assess co-localization. (A and A’) Toll-1::Venus anti-Rab5 labeling. (B and B’) Toll-1::Venus anti-Rab7 labeling. (C and C’) Toll-1::Venus anti-Rab8 labeling. (D and D’) Toll-1::Venus anti-Atg8 labeling. (E and E’) Toll-1::Venus anti-Kdel labeling. (F and F’) Toll-1::Venus anti-Lamp1 labeling. (G and G’) Toll-1::Venus <t>anti-Fmr1</t> labeling. (H) Quantification of co-localization using Pearson’s correlation coefficients between Toll-1::Venus and various organelle markers: stress granules (Fmr1), lysosomes (Lamp1), endoplasmic reticulum (Kdel), autophagosomes (Atg8), early endosomes (Rab5), secretory vesicles (Rab8), and late endosomes (Rab7).
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11g5 n a mouse anti fmrp  (Developmental Studies Hybridoma Bank)
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(A–G’) Co-localization analysis of Toll and subcellular compartment markers in Drosophila S2 cells. Toll-1::Venus was expressed by co-transfection of pActin-GAL4 and p20×UAS-Toll-1::Venus plasmids, followed by immunostaining to assess co-localization. (A and A’) Toll-1::Venus anti-Rab5 labeling. (B and B’) Toll-1::Venus anti-Rab7 labeling. (C and C’) Toll-1::Venus anti-Rab8 labeling. (D and D’) Toll-1::Venus anti-Atg8 labeling. (E and E’) Toll-1::Venus anti-Kdel labeling. (F and F’) Toll-1::Venus anti-Lamp1 labeling. (G and G’) Toll-1::Venus <t>anti-Fmr1</t> labeling. (H) Quantification of co-localization using Pearson’s correlation coefficients between Toll-1::Venus and various organelle markers: stress granules (Fmr1), lysosomes (Lamp1), endoplasmic reticulum (Kdel), autophagosomes (Atg8), early endosomes (Rab5), secretory vesicles (Rab8), and late endosomes (Rab7).
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mouse monoclonal anti-fmrp (clone 1c3)  (Millipore)
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Millipore mouse monoclonal anti-fmrp (clone 1c3)
(A–G’) Co-localization analysis of Toll and subcellular compartment markers in Drosophila S2 cells. Toll-1::Venus was expressed by co-transfection of pActin-GAL4 and p20×UAS-Toll-1::Venus plasmids, followed by immunostaining to assess co-localization. (A and A’) Toll-1::Venus anti-Rab5 labeling. (B and B’) Toll-1::Venus anti-Rab7 labeling. (C and C’) Toll-1::Venus anti-Rab8 labeling. (D and D’) Toll-1::Venus anti-Atg8 labeling. (E and E’) Toll-1::Venus anti-Kdel labeling. (F and F’) Toll-1::Venus anti-Lamp1 labeling. (G and G’) Toll-1::Venus <t>anti-Fmr1</t> labeling. (H) Quantification of co-localization using Pearson’s correlation coefficients between Toll-1::Venus and various organelle markers: stress granules (Fmr1), lysosomes (Lamp1), endoplasmic reticulum (Kdel), autophagosomes (Atg8), early endosomes (Rab5), secretory vesicles (Rab8), and late endosomes (Rab7).
Mouse Monoclonal Anti Fmrp (Clone 1c3), supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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santa cruz sc101048 mouse  (Santa Cruz Biotechnology)
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monoclonal mouse anti fmrp  (Developmental Studies Hybridoma Bank)
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Image Search Results


(A–G’) Co-localization analysis of Toll and subcellular compartment markers in Drosophila S2 cells. Toll-1::Venus was expressed by co-transfection of pActin-GAL4 and p20×UAS-Toll-1::Venus plasmids, followed by immunostaining to assess co-localization. (A and A’) Toll-1::Venus anti-Rab5 labeling. (B and B’) Toll-1::Venus anti-Rab7 labeling. (C and C’) Toll-1::Venus anti-Rab8 labeling. (D and D’) Toll-1::Venus anti-Atg8 labeling. (E and E’) Toll-1::Venus anti-Kdel labeling. (F and F’) Toll-1::Venus anti-Lamp1 labeling. (G and G’) Toll-1::Venus anti-Fmr1 labeling. (H) Quantification of co-localization using Pearson’s correlation coefficients between Toll-1::Venus and various organelle markers: stress granules (Fmr1), lysosomes (Lamp1), endoplasmic reticulum (Kdel), autophagosomes (Atg8), early endosomes (Rab5), secretory vesicles (Rab8), and late endosomes (Rab7).

Journal: bioRxiv

Article Title: An Innate Immune Receptor Toll-1 converts chronic light stress into glial-phagocytosis

doi: 10.1101/2025.09.03.673940

Figure Lengend Snippet: (A–G’) Co-localization analysis of Toll and subcellular compartment markers in Drosophila S2 cells. Toll-1::Venus was expressed by co-transfection of pActin-GAL4 and p20×UAS-Toll-1::Venus plasmids, followed by immunostaining to assess co-localization. (A and A’) Toll-1::Venus anti-Rab5 labeling. (B and B’) Toll-1::Venus anti-Rab7 labeling. (C and C’) Toll-1::Venus anti-Rab8 labeling. (D and D’) Toll-1::Venus anti-Atg8 labeling. (E and E’) Toll-1::Venus anti-Kdel labeling. (F and F’) Toll-1::Venus anti-Lamp1 labeling. (G and G’) Toll-1::Venus anti-Fmr1 labeling. (H) Quantification of co-localization using Pearson’s correlation coefficients between Toll-1::Venus and various organelle markers: stress granules (Fmr1), lysosomes (Lamp1), endoplasmic reticulum (Kdel), autophagosomes (Atg8), early endosomes (Rab5), secretory vesicles (Rab8), and late endosomes (Rab7).

Article Snippet: The following antibodies were used for immunohistochemistry: mAb24B10 (1:25, DSHB), rat antibody to HA (3F10, 1:50, Roche), mouse antibody to Fmr1 (5A11, 1:50, DSHB), rabbit antibody to Lamp1 (1:200, Abcam), mouse antibody to KDEL (10C3, 1:50, Novus), rabbit antibody to Atg8 (1:200, Abcam), rabbit antibody to Rab5 (1:50, Abcam), mouse antibody to Rab8 (1:400, BD Biosciences), and mouse antibody to Rab7 (1:100, DSHB).

Techniques: Cotransfection, Immunostaining, Labeling

Journal: Cell reports

Article Title: CGG repeats in the human FMR1 gene regulate mRNA localization and cellular stress in developing neurons

doi: 10.1016/j.celrep.2024.114330

Figure Lengend Snippet:

Article Snippet: FMRP , Santa Cruz sc101048 (mouse) , ICC (1:100; ) .

Techniques: Marker

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: CGG repeats in the human FMR1 gene regulate mRNA localization and cellular stress in developing neurons

doi: 10.1016/j.celrep.2024.114330

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: FMRP , Santa Cruz sc101048 (mouse) , ICC (1:100; ) .

Techniques: Recombinant, Knock-Out, Viability Assay, ISH Cell Assay, Cloning, Clone Assay, CRISPR, Software