e coli atcc 3518 Search Results


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ATCC escherichia coli atcc 3518
Escherichia Coli Atcc 3518, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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USTC Chuangxin Co Ltd hc-3518 centrifuge
List of apparatus.
Hc 3518 Centrifuge, supplied by USTC Chuangxin Co Ltd, 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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Promega pl-pgc-1 -prom(3518)-luc
List of apparatus.
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List of apparatus.
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Santa Cruz Biotechnology ncz
Fig. 6. cFPGS mRNA transport to cell protrusions is dependent on actin filaments. HeLa cells, deprived of FA for 12 days, were co-transfected with MCP-GFP along with either F-MS2 (A–T) or F-MS2-dmGQ (U–Y). The next day, each cell group was split into different wells and left to grow in FA-free medium for an additional 24 h. Cells were pre-treated for 1 h with 0.1% DMSO (vehicle, A–E), 40 μM VBT (F–J), 10 μM <t>NCZ</t> (K–O), or 250 <t>nM</t> <t>LAN</t> B (P–Y) and supplemented with 2 μM FA for 15 min before fixation and IF microscopy. The localization of cFPGS mRNA is indicated by MCP-GFP (green fluorescence, 488 nm), FLAG-cFPGS protein was detected by an anti-FLAG antibody (red, 405 nm), and F-actin was stained by DyLight 650 Phalloidin (white, 630 nm). T The silhouette of the cells was outlined with a purple line. Cells were scanned using a confocal microscope (×63 magnitude). The scale bars denote 10 μm. Shown are representative images of three independent experiments
Ncz, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DRG International drg toxocara canis elisa (eia-3518) test
Fig. 6. cFPGS mRNA transport to cell protrusions is dependent on actin filaments. HeLa cells, deprived of FA for 12 days, were co-transfected with MCP-GFP along with either F-MS2 (A–T) or F-MS2-dmGQ (U–Y). The next day, each cell group was split into different wells and left to grow in FA-free medium for an additional 24 h. Cells were pre-treated for 1 h with 0.1% DMSO (vehicle, A–E), 40 μM VBT (F–J), 10 μM <t>NCZ</t> (K–O), or 250 <t>nM</t> <t>LAN</t> B (P–Y) and supplemented with 2 μM FA for 15 min before fixation and IF microscopy. The localization of cFPGS mRNA is indicated by MCP-GFP (green fluorescence, 488 nm), FLAG-cFPGS protein was detected by an anti-FLAG antibody (red, 405 nm), and F-actin was stained by DyLight 650 Phalloidin (white, 630 nm). T The silhouette of the cells was outlined with a purple line. Cells were scanned using a confocal microscope (×63 magnitude). The scale bars denote 10 μm. Shown are representative images of three independent experiments
Drg Toxocara Canis Elisa (Eia 3518) Test, supplied by DRG International, 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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PASCO calcium ion-selective electrode ps-3518
Fig. 6. cFPGS mRNA transport to cell protrusions is dependent on actin filaments. HeLa cells, deprived of FA for 12 days, were co-transfected with MCP-GFP along with either F-MS2 (A–T) or F-MS2-dmGQ (U–Y). The next day, each cell group was split into different wells and left to grow in FA-free medium for an additional 24 h. Cells were pre-treated for 1 h with 0.1% DMSO (vehicle, A–E), 40 μM VBT (F–J), 10 μM <t>NCZ</t> (K–O), or 250 <t>nM</t> <t>LAN</t> B (P–Y) and supplemented with 2 μM FA for 15 min before fixation and IF microscopy. The localization of cFPGS mRNA is indicated by MCP-GFP (green fluorescence, 488 nm), FLAG-cFPGS protein was detected by an anti-FLAG antibody (red, 405 nm), and F-actin was stained by DyLight 650 Phalloidin (white, 630 nm). T The silhouette of the cells was outlined with a purple line. Cells were scanned using a confocal microscope (×63 magnitude). The scale bars denote 10 μm. Shown are representative images of three independent experiments
Calcium Ion Selective Electrode Ps 3518, supplied by PASCO, 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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Becton Dickinson flow cytometry becton dickinson facscalibur
Fig. 6. cFPGS mRNA transport to cell protrusions is dependent on actin filaments. HeLa cells, deprived of FA for 12 days, were co-transfected with MCP-GFP along with either F-MS2 (A–T) or F-MS2-dmGQ (U–Y). The next day, each cell group was split into different wells and left to grow in FA-free medium for an additional 24 h. Cells were pre-treated for 1 h with 0.1% DMSO (vehicle, A–E), 40 μM VBT (F–J), 10 μM <t>NCZ</t> (K–O), or 250 <t>nM</t> <t>LAN</t> B (P–Y) and supplemented with 2 μM FA for 15 min before fixation and IF microscopy. The localization of cFPGS mRNA is indicated by MCP-GFP (green fluorescence, 488 nm), FLAG-cFPGS protein was detected by an anti-FLAG antibody (red, 405 nm), and F-actin was stained by DyLight 650 Phalloidin (white, 630 nm). T The silhouette of the cells was outlined with a purple line. Cells were scanned using a confocal microscope (×63 magnitude). The scale bars denote 10 μm. Shown are representative images of three independent experiments
Flow Cytometry Becton Dickinson Facscalibur, supplied by Becton Dickinson, 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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Image Search Results


List of apparatus.

Journal: Polymers

Article Title: Preparation and Hydrogen Storage Characteristics of Surfactant-Modified Graphene

doi: 10.3390/polym10111220

Figure Lengend Snippet: List of apparatus.

Article Snippet: HC-3518 Centrifuge , China USTC Chuangxin Co., Ltd., Hefei, Anhui, China.

Techniques:

Fig. 6. cFPGS mRNA transport to cell protrusions is dependent on actin filaments. HeLa cells, deprived of FA for 12 days, were co-transfected with MCP-GFP along with either F-MS2 (A–T) or F-MS2-dmGQ (U–Y). The next day, each cell group was split into different wells and left to grow in FA-free medium for an additional 24 h. Cells were pre-treated for 1 h with 0.1% DMSO (vehicle, A–E), 40 μM VBT (F–J), 10 μM NCZ (K–O), or 250 nM LAN B (P–Y) and supplemented with 2 μM FA for 15 min before fixation and IF microscopy. The localization of cFPGS mRNA is indicated by MCP-GFP (green fluorescence, 488 nm), FLAG-cFPGS protein was detected by an anti-FLAG antibody (red, 405 nm), and F-actin was stained by DyLight 650 Phalloidin (white, 630 nm). T The silhouette of the cells was outlined with a purple line. Cells were scanned using a confocal microscope (×63 magnitude). The scale bars denote 10 μm. Shown are representative images of three independent experiments

Journal: BMC biology

Article Title: Folylpolyglutamate synthetase mRNA G-quadruplexes regulate its cell protrusion localization and enhance a cancer cell invasive phenotype upon folate repletion.

doi: 10.1186/s12915-023-01525-1

Figure Lengend Snippet: Fig. 6. cFPGS mRNA transport to cell protrusions is dependent on actin filaments. HeLa cells, deprived of FA for 12 days, were co-transfected with MCP-GFP along with either F-MS2 (A–T) or F-MS2-dmGQ (U–Y). The next day, each cell group was split into different wells and left to grow in FA-free medium for an additional 24 h. Cells were pre-treated for 1 h with 0.1% DMSO (vehicle, A–E), 40 μM VBT (F–J), 10 μM NCZ (K–O), or 250 nM LAN B (P–Y) and supplemented with 2 μM FA for 15 min before fixation and IF microscopy. The localization of cFPGS mRNA is indicated by MCP-GFP (green fluorescence, 488 nm), FLAG-cFPGS protein was detected by an anti-FLAG antibody (red, 405 nm), and F-actin was stained by DyLight 650 Phalloidin (white, 630 nm). T The silhouette of the cells was outlined with a purple line. Cells were scanned using a confocal microscope (×63 magnitude). The scale bars denote 10 μm. Shown are representative images of three independent experiments

Article Snippet: NCZ (#sc-3518), LAN B (#sc203318), Y27632 (#sc-281642), and CyMl (#sc-500804) were from Santa Cruz Biotechnology, Dallas, TX, USA.

Techniques: Transfection, Microscopy, Fluorescence, Staining