Category:Fluorescent antibody technique

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Subcategories

This category has the following 4 subcategories, out of 4 total.

D

I

Indirect fluorescent antibody stain (4 F)
Indirect fluorescent antibody technique (13 F)

Media in category "Fluorescent antibody technique"

The following 200 files are in this category, out of 306 total.

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A-Highly-Conserved-Poc1-Protein-Characterized-in-Embryos-of-the-Hydrozoan-Clytia-hemisphaerica-pone.0013994.s004.ogv 6.7 s, 1,020 × 340; 1.02 MB
A-Highly-Conserved-Poc1-Protein-Characterized-in-Embryos-of-the-Hydrozoan-Clytia-hemisphaerica-pone.0013994.s005.ogv 14 s, 478 × 346; 6.51 MB
A-Kinome-RNAi-Screen-Identified-AMPK-as-Promoting-Poxvirus-Entry-through-the-Control-of-Actin-ppat.1000954.s017.ogv 1 min 2 s, 640 × 480; 6.45 MB
A-Kinome-RNAi-Screen-Identified-AMPK-as-Promoting-Poxvirus-Entry-through-the-Control-of-Actin-ppat.1000954.s018.ogv 47 s, 640 × 480; 3.29 MB
A-Model-of-Ischemia-Induced-Neuroblast-Activation-in-the-Adult-Subventricular-Zone-pone.0005278.s009.ogv 5.2 s, 976 × 816; 2.77 MB
A-Model-of-Ischemia-Induced-Neuroblast-Activation-in-the-Adult-Subventricular-Zone-pone.0005278.s010.ogv 20 s, 356 × 314; 175 KB
A-Model-of-Ischemia-Induced-Neuroblast-Activation-in-the-Adult-Subventricular-Zone-pone.0005278.s011.ogv 20 s, 356 × 314; 183 KB
A-negative-feedback-loop-controls-NMDA-receptor-function-in-cortical-interneurons-via-neuregulin-ncomms8222-s2.ogv 30 s, 512 × 512; 1.15 MB
A-negative-feedback-loop-controls-NMDA-receptor-function-in-cortical-interneurons-via-neuregulin-ncomms8222-s3.ogv 25 s, 512 × 512; 2.72 MB
A-negative-feedback-loop-controls-NMDA-receptor-function-in-cortical-interneurons-via-neuregulin-ncomms8222-s4.ogv 25 s, 512 × 512; 821 KB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s001.ogv 5.3 s, 315 × 306; 271 KB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s002.ogv 8.9 s, 240 × 240; 160 KB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s003.ogv 9.9 s, 378 × 258; 230 KB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s004.ogv 8.6 s, 246 × 246; 125 KB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s005.ogv 17 s, 374 × 441; 2.29 MB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s006.ogv 17 s, 364 × 307; 1.52 MB
A-Novel-Microtubule-Inhibitor-4SC-207-with-Anti-Proliferative-Activity-in-Taxane-Resistant-Cells-pone.0079594.s007.ogv 17 s, 374 × 298; 1.48 MB
A-Novel-Role-for-the-Centrosomal-Protein-Pericentrin-in-Regulation-of-Insulin-Secretory-Vesicle-pone.0011812.s004.ogv 17 s, 320 × 240; 445 KB
A-Secreted-BMP-Antagonist-Cer1-Fine-Tunes-the-Spatial-Organization-of-the-Ureteric-Bud-Tree-during-pone.0027676.s010.ogv 30 s, 950 × 355; 3.2 MB
A-Secreted-BMP-Antagonist-Cer1-Fine-Tunes-the-Spatial-Organization-of-the-Ureteric-Bud-Tree-during-pone.0027676.s011.ogv 21 s, 820 × 475; 4.52 MB
AMA ANTIBODIES.jpg 1,877 × 1,533; 4.09 MB
Anaplasma-phagocytophilum-Ats-1-Is-Imported-into-Host-Cell-Mitochondria-and-Interferes-with-ppat.1000774.s004.ogv 3.6 s, 494 × 480; 296 KB
Arsenic-trioxide-alters-the-differentiation-of-mouse-embryonic-stem-cell-into-cardiomyocytes-srep14993-s2.ogv 42 s, 320 × 240; 2.8 MB
Arsenic-trioxide-alters-the-differentiation-of-mouse-embryonic-stem-cell-into-cardiomyocytes-srep14993-s3.ogv 59 s, 320 × 240; 2.97 MB
Arsenic-trioxide-alters-the-differentiation-of-mouse-embryonic-stem-cell-into-cardiomyocytes-srep14993-s4.ogv 42 s, 320 × 240; 2.22 MB
Arsenic-trioxide-alters-the-differentiation-of-mouse-embryonic-stem-cell-into-cardiomyocytes-srep14993-s5.ogv 45 s, 320 × 240; 805 KB
Asparagine-requirement-in-Plasmodium-berghei-as-a-target-to-prevent-malaria-transmission-and-liver-ncomms9775-s2.ogv 15 s, 400 × 400; 5.57 MB
Asparagine-requirement-in-Plasmodium-berghei-as-a-target-to-prevent-malaria-transmission-and-liver-ncomms9775-s3.ogv 15 s, 400 × 400; 8 MB
Asparagine-requirement-in-Plasmodium-berghei-as-a-target-to-prevent-malaria-transmission-and-liver-ncomms9775-s4.ogv 15 s, 398 × 400; 9.19 MB
Asparagine-requirement-in-Plasmodium-berghei-as-a-target-to-prevent-malaria-transmission-and-liver-ncomms9775-s5.ogv 15 s, 400 × 398; 7.1 MB
Asparagine-requirement-in-Plasmodium-berghei-as-a-target-to-prevent-malaria-transmission-and-liver-ncomms9775-s6.ogv 15 s, 400 × 400; 6.01 MB
Asymmetry-of-Early-Endosome-Distribution-in-C.-elegans-Embryos-pone.0000493.s001.ogv 7.0 s, 548 × 198; 3.11 MB
Bacillus-subtilis-MreB-Orthologs-Self-Organize-into-Filamentous-Structures-underneath-the-Cell-pone.0027035.s001.ogv 9.0 s, 166 × 168; 53 KB
Bacillus-subtilis-MreB-Orthologs-Self-Organize-into-Filamentous-Structures-underneath-the-Cell-pone.0027035.s002.ogv 9.0 s, 223 × 228; 32 KB
Bacillus-subtilis-MreB-Orthologs-Self-Organize-into-Filamentous-Structures-underneath-the-Cell-pone.0027035.s003.ogv 14 s, 206 × 224; 97 KB
Bacillus-subtilis-MreB-Orthologs-Self-Organize-into-Filamentous-Structures-underneath-the-Cell-pone.0027035.s004.ogv 8.0 s, 315 × 294; 448 KB
Bacillus-subtilis-MreB-Orthologs-Self-Organize-into-Filamentous-Structures-underneath-the-Cell-pone.0027035.s005.ogv 8.0 s, 327 × 321; 117 KB
Bim-and-Bmf-Synergize-To-Induce-Apoptosis-in-Neisseria-Gonorrhoeae-Infection-ppat.1000348.s011.ogv 1.1 s, 328 × 306; 51 KB
Bim-and-Bmf-Synergize-To-Induce-Apoptosis-in-Neisseria-Gonorrhoeae-Infection-ppat.1000348.s012.ogv 11 s, 300 × 294; 936 KB
Bub1-autophosphorylation-feeds-back-to-regulate-kinetochore-docking-and-promote-localized-substrate-ncomms9364-s3.ogv 3.0 s, 67 × 65; 17 KB
Bub1-autophosphorylation-feeds-back-to-regulate-kinetochore-docking-and-promote-localized-substrate-ncomms9364-s4.ogv 3.4 s, 91 × 79; 16 KB
Bub1-autophosphorylation-feeds-back-to-regulate-kinetochore-docking-and-promote-localized-substrate-ncomms9364-s5.ogv 20 s, 80 × 80; 44 KB
Capture-of-Neuroepithelial-Like-Stem-Cells-from-Pluripotent-Stem-Cells-Provides-a-Versatile-System-pone.0029597.s009.ogv 23 s, 1,152 × 924; 10.99 MB
Cdk5-mediated-phosphorylation-of-RapGEF2-controls-neuronal-migration-in-the-developing-cerebral-ncomms5826-s2.ogv 7.7 s, 480 × 480; 1.46 MB
Cdk5-mediated-phosphorylation-of-RapGEF2-controls-neuronal-migration-in-the-developing-cerebral-ncomms5826-s3.ogv 7.7 s, 480 × 480; 1.45 MB
Cell-Cycle-Phase-Regulates-Glucocorticoid-Receptor-Function-pone.0022289.s001.ogv 9.7 s, 640 × 480; 1.12 MB
Cell-movement-pbio.1001320.s011.ogv 8.4 s, 512 × 512; 106 KB
Cell-movement-pbio.1001320.s012.ogv 25 s, 1,060 × 793; 123 KB
Cell-movement-pbio.1001320.s013.ogv 24 s, 786 × 576; 2.16 MB
Characterization-of-Eag1-Channel-Lateral-Mobility-in-Rat-Hippocampal-Cultures-by-Single-Particle-pone.0008858.s003.ogv 1 min 30 s, 29 × 52; 59 KB
Characterization-of-Eag1-Channel-Lateral-Mobility-in-Rat-Hippocampal-Cultures-by-Single-Particle-pone.0008858.s004.ogv 1 min 30 s, 277 × 86; 709 KB
Chromosomal-Instability-by-Inefficient-Mps1-Auto-Activation-Due-to-a-Weakened-Mitotic-Checkpoint-pone.0002415.s002.ogv 3.7 s, 180 × 180; 24 KB
Chromosomal-Instability-by-Inefficient-Mps1-Auto-Activation-Due-to-a-Weakened-Mitotic-Checkpoint-pone.0002415.s003.ogv 8.7 s, 180 × 180; 38 KB
Complement-Receptor-1-Is-a-Sialic-Acid-Independent-Erythrocyte-Receptor-of-Plasmodium-falciparum-ppat.1000968.s005.ogv 19 s, 384 × 288; 92 KB
Complement-Receptor-1-Is-a-Sialic-Acid-Independent-Erythrocyte-Receptor-of-Plasmodium-falciparum-ppat.1000968.s006.ogv 19 s, 384 × 288; 94 KB
Complement-Receptor-1-Is-a-Sialic-Acid-Independent-Erythrocyte-Receptor-of-Plasmodium-falciparum-ppat.1000968.s007.ogv 19 s, 384 × 288; 169 KB
Complement-Receptor-1-Is-a-Sialic-Acid-Independent-Erythrocyte-Receptor-of-Plasmodium-falciparum-ppat.1000968.s008.ogv 19 s, 384 × 288; 134 KB
Complement-Receptor-1-Is-a-Sialic-Acid-Independent-Erythrocyte-Receptor-of-Plasmodium-falciparum-ppat.1000968.s009.ogv 19 s, 384 × 288; 117 KB
Complement-Receptor-1-Is-a-Sialic-Acid-Independent-Erythrocyte-Receptor-of-Plasmodium-falciparum-ppat.1000968.s010.ogv 19 s, 384 × 288; 84 KB
Coordination-of-glioblastoma-cell-motility-by-PKCι-1476-4598-9-233-S2.ogv 25 s, 312 × 240; 484 KB
Coordination-of-glioblastoma-cell-motility-by-PKCι-1476-4598-9-233-S3.ogv 25 s, 312 × 240; 793 KB
Coordination-of-glioblastoma-cell-motility-by-PKCι-1476-4598-9-233-S4.ogv 25 s, 312 × 240; 346 KB
CRIM1-Complexes-with-ß-catenin-and-Cadherins-Stabilizes-Cell-Cell-Junctions-and-Is-Critical-for-pone.0032635.s002.ogv 5.4 s, 1,350 × 729; 554 KB
CRIM1-Complexes-with-ß-catenin-and-Cadherins-Stabilizes-Cell-Cell-Junctions-and-Is-Critical-for-pone.0032635.s003.ogv 5.4 s, 1,237 × 1,029; 655 KB
Differential-Association-between-HERG-and-KCNE1-or-KCNE2-pone.0000933.s001.ogv 5.1 s, 300 × 298; 226 KB
Differential-Association-between-HERG-and-KCNE1-or-KCNE2-pone.0000933.s002.ogv 5.1 s, 184 × 244; 122 KB
Distinctive-Left-Sided-Distribution-of-Adrenergic-Derived-Cells-in-the-Adult-Mouse-Heart-pone.0022811.s001.ogv 49 s, 348 × 312; 1.7 MB
Distinctive-Left-Sided-Distribution-of-Adrenergic-Derived-Cells-in-the-Adult-Mouse-Heart-pone.0022811.s002.ogv 55 s, 348 × 312; 3.63 MB
Early-transplantation-of-human-immature-dental-pulp-stem-cells-from-baby-teeth-to-golden-retriever-1479-5876-6-35-S1.ogv 13 s, 640 × 480; 7.4 MB
Early-transplantation-of-human-immature-dental-pulp-stem-cells-from-baby-teeth-to-golden-retriever-1479-5876-6-35-S2.ogv 12 s, 640 × 480; 7.69 MB
Early-transplantation-of-human-immature-dental-pulp-stem-cells-from-baby-teeth-to-golden-retriever-1479-5876-6-35-S3.ogv 4.3 s, 640 × 480; 1.35 MB
Efferent-Control-of-the-Electrical-and-Mechanical-Properties-of-Hair-Cells-in-the-Bullfrog's-pone.0013777.s004.ogv 1 min 34 s, 640 × 640; 3.66 MB
Efferent-Control-of-the-Electrical-and-Mechanical-Properties-of-Hair-Cells-in-the-Bullfrog's-pone.0013777.s005.ogv 24 s, 447 × 403; 202 KB
Efferent-Control-of-the-Electrical-and-Mechanical-Properties-of-Hair-Cells-in-the-Bullfrog's-pone.0013777.s006.ogv 6.8 s, 512 × 512; 2.17 MB
ER-Bound-Protein-Tyrosine-Phosphatase-PTP1B-Interacts-with-Src-at-the-Plasma-MembraneSubstrate-pone.0038948.s007.ogv 4.0 s, 312 × 332; 77 KB
Expression-of-P.-falciparum-var-Genes-Involves-Exchange-of-the-Histone-Variant-H2A.Z-at-the-Promoter-ppat.1001292.s011.ogv 6.2 s, 320 × 240; 23 KB
FleA-Expression-in-Aspergillus-fumigatus-Is-Recognized-by-Fucosylated-Structures-on-Mucins-and-ppat.1005555.s003.ogv 2.4 s, 312 × 312; 31 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s008.ogv 15 s, 720 × 576; 452 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s009.ogv 38 s, 720 × 576; 2 MB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s010.ogv 6.3 s, 720 × 576; 201 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s012.ogv 26 s, 720 × 576; 1.48 MB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s013.ogv 12 s, 720 × 576; 391 KB
Functional-Analysis-of-the-Leading-Malaria-Vaccine-Candidate-AMA-1-Reveals-an-Essential-Role-for-ppat.1000322.s014.ogv 38 s, 720 × 576; 2.17 MB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s001.ogv 21 s, 320 × 240; 165 KB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s002.ogv 8.5 s, 384 × 288; 147 KB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s003.ogv 9.8 s, 320 × 240; 142 KB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s004.ogv 19 s, 320 × 240; 283 KB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s005.ogv 30 s, 320 × 240; 1.47 MB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s006.ogv 40 s, 320 × 240; 1.69 MB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s007.ogv 40 s, 320 × 240; 1.69 MB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s008.ogv 33 s, 320 × 240; 1 MB
Fungal-Cell-Gigantism-during-Mammalian-Infection-ppat.1000945.s009.ogv 41 s, 320 × 240; 1.82 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s10.ogv 8.0 s, 1,440 × 480; 954 KB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s11.ogv 3.4 s, 960 × 480; 821 KB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s12.ogv 11 s, 1,445 × 480; 1.53 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s13.ogv 6.0 s, 1,022 × 480; 1.73 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s2.ogv 4.8 s, 1,440 × 480; 1.27 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s3.ogv 30 s, 960 × 480; 5.09 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s4.ogv 10 s, 960 × 480; 2.56 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s7.ogv 9.8 s, 642 × 480; 1.8 MB
Gap-geometry-dictates-epithelial-closure-efficiency-ncomms8683-s9.ogv 6.0 s, 1,440 × 480; 777 KB
Greatly-attenuated-experimental-autoimmune-encephalomyelitis-in-aquaporin-4-knockout-mice-1471-2202-10-94-S1.ogv 8.0 s, 660 × 280; 562 KB
Hematopoietic-Stem-Cell-Cytokines-and-Fibroblast-Growth-factor-2-Stimulate-Human-Endothelial-Cell-pone.0085147.s001.ogv 0.0 s, 688 × 595; 11.56 MB
Hematopoietic-Stem-Cell-Cytokines-and-Fibroblast-Growth-factor-2-Stimulate-Human-Endothelial-Cell-pone.0085147.s002.ogv 0.0 s, 735 × 594; 18.93 MB
Hematopoietic-Stem-Cell-Cytokines-and-Fibroblast-Growth-factor-2-Stimulate-Human-Endothelial-Cell-pone.0085147.s003.ogv 0.0 s, 688 × 595; 17.74 MB
Hematopoietic-Stem-Cell-Cytokines-and-Fibroblast-Growth-factor-2-Stimulate-Human-Endothelial-Cell-pone.0085147.s004.ogv 0.0 s, 735 × 594; 12.35 MB
Hematopoietic-Stem-Cell-Cytokines-and-Fibroblast-Growth-factor-2-Stimulate-Human-Endothelial-Cell-pone.0085147.s005.ogv 0.0 s, 688 × 595; 2.25 MB
Hematopoietic-Stem-Cell-Cytokines-and-Fibroblast-Growth-factor-2-Stimulate-Human-Endothelial-Cell-pone.0085147.s006.ogv 20 s, 688 × 595; 6.31 MB
Herpes-Simplex-Virus-Dances-with-Amyloid-Precursor-Protein-while-Exiting-the-Cell-pone.0017966.s010.ogv 23 s, 598 × 314; 313 KB
Herpes-Simplex-Virus-Dances-with-Amyloid-Precursor-Protein-while-Exiting-the-Cell-pone.0017966.s012.ogv 1.8 s, 550 × 228; 116 KB
Herpes-Simplex-Virus-Dances-with-Amyloid-Precursor-Protein-while-Exiting-the-Cell-pone.0017966.s013.ogv 18 s, 117 × 106; 448 KB
Herpes-Simplex-Virus-Dances-with-Amyloid-Precursor-Protein-while-Exiting-the-Cell-pone.0017966.s014.ogv 28 s, 147 × 258; 1.95 MB
Herpes-Simplex-Virus-Dances-with-Amyloid-Precursor-Protein-while-Exiting-the-Cell-pone.0017966.s015.ogv 4.8 s, 348 × 392; 893 KB
Human-Engineered-Heart-Tissue-as-a-Versatile-Tool-in-Basic-Research-and-Preclinical-Toxicology-pone.0026397.s004.ogv 14 s, 720 × 576; 1.65 MB
Human-Engineered-Heart-Tissue-as-a-Versatile-Tool-in-Basic-Research-and-Preclinical-Toxicology-pone.0026397.s005.ogv 1 min 0 s, 640 × 480; 1.22 MB
In-Situ-Dividing-and-Phagocytosing-Retinal-Microglia-Express-Nestin-Vimentin-and-NG2-In-Vivo-pone.0022408.s001.ogv 5.0 s, 1,245 × 1,245; 396 KB
In-Situ-Dividing-and-Phagocytosing-Retinal-Microglia-Express-Nestin-Vimentin-and-NG2-In-Vivo-pone.0022408.s002.ogv 9.0 s, 1,245 × 1,245; 1.14 MB
In-Situ-Dividing-and-Phagocytosing-Retinal-Microglia-Express-Nestin-Vimentin-and-NG2-In-Vivo-pone.0022408.s003.ogv 5.0 s, 696 × 696; 135 KB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s008.ogv 10 s, 513 × 512; 3.45 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s009.ogv 10 s, 511 × 512; 3.78 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s010.ogv 17 s, 500 × 445; 3.43 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s011.ogv 10 s, 406 × 442; 2.2 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s012.ogv 7.5 s, 800 × 403; 2.87 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s013.ogv 12 s, 512 × 514; 2.48 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s014.ogv 8.0 s, 512 × 515; 3.1 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s015.ogv 10 s, 700 × 700; 5.63 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s016.ogv 10 s, 395 × 455; 1.94 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s017.ogv 22 s, 580 × 479; 4.12 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s018.ogv 7.5 s, 800 × 403; 3.02 MB
In-Vivo-Approaches-Reveal-a-Key-Role-for-DCs-in-CD4+-T-Cell-Activation-and-Parasite-Clearance-ppat.1004598.s019.ogv 10 s, 890 × 638; 3.25 MB
Influenza-A-Virus-Assembly-Intermediates-Fuse-in-the-Cytoplasm-ppat.1003971.s007.ogv 38 s, 280 × 240; 8.95 MB
Influenza-A-Virus-Assembly-Intermediates-Fuse-in-the-Cytoplasm-ppat.1003971.s008.ogv 37 s, 360 × 360; 14.64 MB
Influenza-A-Virus-Assembly-Intermediates-Fuse-in-the-Cytoplasm-ppat.1003971.s009.ogv 14 s, 1,024 × 1,024; 12.14 MB
Kaposi's-Sarcoma-Associated-Herpesvirus-ORF45-Interacts-with-Kinesin-2-Transporting-Viral-Capsid-ppat.1000332.s002.ogv 4.4 s, 488 × 480; 409 KB
Kaposi's-Sarcoma-Associated-Herpesvirus-ORF45-Interacts-with-Kinesin-2-Transporting-Viral-Capsid-ppat.1000332.s003.ogv 4.4 s, 496 × 480; 775 KB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s10.ogv 7.0 s, 640 × 480; 458 KB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s11.ogv 8.0 s, 640 × 480; 301 KB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s2.ogv 4.0 s, 854 × 480; 279 KB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s3.ogv 10 s, 854 × 480; 7.13 MB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s4.ogv 10 s, 854 × 480; 11.56 MB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s5.ogv 9.0 s, 854 × 480; 1.24 MB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s6.ogv 6.0 s, 854 × 480; 1.88 MB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s7.ogv 9.0 s, 854 × 480; 1.8 MB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s8.ogv 6.0 s, 854 × 480; 787 KB
Local-3D-matrix-microenvironment-regulates-cell-migration-through-spatiotemporal-dynamics-of-ncomms9720-s9.ogv 6.0 s, 854 × 480; 1.12 MB
Loss-of-Myotubularin-Function-Results-in-T-Tubule-Disorganization-in-Zebrafish-and-Human-Myotubular-pgen.1000372.s006.ogv 7.5 s, 760 × 540; 346 KB
Loss-of-Myotubularin-Function-Results-in-T-Tubule-Disorganization-in-Zebrafish-and-Human-Myotubular-pgen.1000372.s007.ogv 7.5 s, 760 × 540; 313 KB
Loss-of-Myotubularin-Function-Results-in-T-Tubule-Disorganization-in-Zebrafish-and-Human-Myotubular-pgen.1000372.s008.ogv 1.6 s, 640 × 480; 131 KB
Loss-of-Myotubularin-Function-Results-in-T-Tubule-Disorganization-in-Zebrafish-and-Human-Myotubular-pgen.1000372.s009.ogv 10 s, 320 × 240; 163 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s008.ogv 20 s, 281 × 234; 297 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s009.ogv 20 s, 266 × 265; 544 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s010.ogv 12 s, 356 × 332; 281 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s011.ogv 12 s, 288 × 304; 227 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s012.ogv 12 s, 408 × 306; 430 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s013.ogv 12 s, 308 × 284; 133 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s014.ogv 14 s, 486 × 418; 1,003 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s015.ogv 14 s, 372 × 404; 659 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s016.ogv 11 s, 304 × 280; 192 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s017.ogv 14 s, 490 × 504; 957 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s018.ogv 14 s, 416 × 456; 862 KB
Lung-Epithelial-Injury-by-B.-Anthracis-Lethal-Toxin-Is-Caused-by-MKK-Dependent-Loss-of-Cytoskeletal-pone.0004755.s019.ogv 12 s, 384 × 312; 275 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s001.ogv 6.9 s, 130 × 260; 153 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s002.ogv 8.8 s, 130 × 260; 240 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s003.ogv 6.8 s, 130 × 130; 18 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s004.ogv 4.5 s, 130 × 130; 31 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s005.ogv 7.4 s, 150 × 150; 74 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s006.ogv 7.4 s, 150 × 150; 26 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s007.ogv 4.8 s, 150 × 150; 45 KB
Meiotic-Regulation-of-TPX2-Protein-Levels-Governs-Cell-Cycle-Progression-in-Mouse-Oocytes-pone.0003338.s008.ogv 5.1 s, 190 × 190; 43 KB
Membrane-Bound-Monomer-of-Staphylococcal-α-Hemolysin-Induces-Caspase-Activation-and-Apoptotic-Cell-pone.0006293.s001.ogv 4.0 s, 393 × 213; 2.45 MB
Membrane-Bound-Monomer-of-Staphylococcal-α-Hemolysin-Induces-Caspase-Activation-and-Apoptotic-Cell-pone.0006293.s002.ogv 4.0 s, 392 × 225; 1.91 MB
Membrane-Bound-Monomer-of-Staphylococcal-α-Hemolysin-Induces-Caspase-Activation-and-Apoptotic-Cell-pone.0006293.s003.ogv 4.0 s, 362 × 389; 6.1 MB
Membrane-Bound-Monomer-of-Staphylococcal-α-Hemolysin-Induces-Caspase-Activation-and-Apoptotic-Cell-pone.0006293.s004.ogv 4.0 s, 355 × 380; 4.73 MB
Membrane-Bound-Monomer-of-Staphylococcal-α-Hemolysin-Induces-Caspase-Activation-and-Apoptotic-Cell-pone.0006293.s005.ogv 6.0 s, 255 × 248; 3.09 MB
Membrane-Bound-Monomer-of-Staphylococcal-α-Hemolysin-Induces-Caspase-Activation-and-Apoptotic-Cell-pone.0006293.s006.ogv 4.0 s, 287 × 401; 4.84 MB
Multi-Level-Communication-of-Human-Retinal-Pigment-Epithelial-Cells-via-Tunneling-Nanotubes-pone.0033195.s001.ogv 15 s, 896 × 476; 840 KB
Multimodal-stimulus-coding-by-a-gustatory-sensory-neuron-in-Drosophila-larvae-ncomms10687-s3.ogv 9.1 s, 1,024 × 1,024; 1.05 MB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S1.ogv 8.3 s, 429 × 424; 548 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S10.ogv 12 s, 536 × 412; 2.79 MB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S11.ogv 12 s, 536 × 512; 1.68 MB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S12.ogv 6.1 s, 536 × 512; 1.86 MB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S2.ogv 8.3 s, 535 × 512; 217 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S3.ogv 10 s, 535 × 512; 54 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S4.ogv 10 s, 535 × 512; 684 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S5.ogv 10 s, 535 × 512; 260 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S6.ogv 10 s, 535 × 512; 263 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S7.ogv 5.2 s, 535 × 512; 122 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S8.ogv 6.8 s, 535 × 512; 579 KB
Myosin-Vb-functions-as-a-dynamic-tether-for-peripheral-endocytic-compartments-during-transferrin-1471-2121-9-44-S9.ogv 8.3 s, 226 × 214; 87 KB
Neisseria-meningitidis-Differentially-Controls-Host-Cell-Motility-through-PilC1-and-PilC2-pone.0006834.s003.ogv 22 s, 300 × 225; 2.5 MB
Neisseria-meningitidis-Differentially-Controls-Host-Cell-Motility-through-PilC1-and-PilC2-pone.0006834.s004.ogv 21 s, 300 × 225; 1.93 MB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s1.ogv 18 s, 320 × 240; 80 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s2.ogv 18 s, 1,024 × 768; 463 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s3.ogv 18 s, 1,024 × 768; 406 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s4.ogv 50 s, 640 × 480; 206 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s5.ogv 50 s, 640 × 480; 254 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s6.ogv 50 s, 640 × 480; 231 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s7.ogv 50 s, 640 × 480; 250 KB
Novel-method-for-immunofluorescence-staining-of-mammalian-eggs-using-non-contact-alternating-srep15371-s8.ogv 29 s, 320 × 240; 1.36 MB
Nuclear-envelope-associated-endosomes-deliver-surface-proteins-to-the-nucleus-ncomms9218-s2.ogv 26 s, 768 × 576; 4.38 MB

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