simplepci Search Results


compix simplepci  (Compix Inc)
90
Compix Inc compix simplepci
Compix Simplepci, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/compix simplepci/product/Compix Inc
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compix simplepci - by Bioz Stars, 2026-06
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simplepci software  (Compix Inc)
90
Compix Inc simplepci software
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci Software, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci software/product/Compix Inc
Average 90 stars, based on 1 article reviews
simplepci software - by Bioz Stars, 2026-06
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simplepci  (Compix Inc)
90
Compix Inc simplepci
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci/product/Compix Inc
Average 90 stars, based on 1 article reviews
simplepci - by Bioz Stars, 2026-06
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simplepci 4.0 software  (Compix Inc)
90
Compix Inc simplepci 4.0 software
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci 4.0 Software, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci 4.0 software/product/Compix Inc
Average 90 stars, based on 1 article reviews
simplepci 4.0 software - by Bioz Stars, 2026-06
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simplepci  (Hamamatsu)
90
Hamamatsu simplepci
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci, supplied by Hamamatsu, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci/product/Hamamatsu
Average 90 stars, based on 1 article reviews
simplepci - by Bioz Stars, 2026-06
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simplepci image analysis system ver.5  (Compix Inc)
90
Compix Inc simplepci image analysis system ver.5
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci Image Analysis System Ver.5, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci image analysis system ver.5/product/Compix Inc
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simplepci image analysis system ver.5 - by Bioz Stars, 2026-06
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simplepci 6.0 software  (Hamamatsu)
90
Hamamatsu simplepci 6.0 software
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci 6.0 Software, supplied by Hamamatsu, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci 6.0 software/product/Hamamatsu
Average 90 stars, based on 1 article reviews
simplepci 6.0 software - by Bioz Stars, 2026-06
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c-imaging (simplepci  (Hamamatsu)
90
Hamamatsu c-imaging (simplepci
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
C Imaging (Simplepci, supplied by Hamamatsu, 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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c-imaging (simplepci - by Bioz Stars, 2026-06
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hamamatsu simplepci software  (Hamamatsu)
90
Hamamatsu hamamatsu simplepci software
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Hamamatsu Simplepci Software, supplied by Hamamatsu, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hamamatsu simplepci software/product/Hamamatsu
Average 90 stars, based on 1 article reviews
hamamatsu simplepci software - by Bioz Stars, 2026-06
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high-resolution software simplepci version 5.3  (Compix Inc)
90
Compix Inc high-resolution software simplepci version 5.3
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
High Resolution Software Simplepci Version 5.3, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/high-resolution software simplepci version 5.3/product/Compix Inc
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high-resolution software simplepci version 5.3 - by Bioz Stars, 2026-06
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simplepci 6.0  (Compix Inc)
90
Compix Inc simplepci 6.0
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci 6.0, supplied by Compix Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/simplepci 6.0/product/Compix Inc
Average 90 stars, based on 1 article reviews
simplepci 6.0 - by Bioz Stars, 2026-06
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simplepci imaging system version 5.2.1.1609  (Compix Inc)
90
Compix Inc simplepci imaging system version 5.2.1.1609
Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using <t>SimplePCI</t> Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.
Simplepci Imaging System Version 5.2.1.1609, supplied by Compix Inc, 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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simplepci imaging system version 5.2.1.1609 - by Bioz Stars, 2026-06
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Image Search Results


Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using SimplePCI Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.

Journal: The Journal of Cell Biology

Article Title: Rap1 controls cell adhesion and cell motility through the regulation of myosin II

doi: 10.1083/jcb.200607072

Figure Lengend Snippet: Subcellular localization of GFP-Phg2 and morphology of phg2 -null cells. (A) Translocation of GFP-Phg2 to the cell cortex in response to cAMP stimulation. The fluorescence intensity on the plasma membrane fraction or in the cytosol fraction was quantitated using SimplePCI Imaging Systems. The graphs represent mean values of 10 cells from two separate experiments. (B) Localization of GFP-Phg2 in the migrating cells. The arrow indicates the direction of movement. (C) Morphology of phg2 -null cells. Vegetative cells were plated in HL5 growth medium or Na/K phosphate buffer on a plate with a hole covered by a glass coverslip and were imaged. phg2 -null cells show lamellipodia-like (white arrows) or filopodia-like structures (black arrows) compared with wild-type cells.

Article Snippet: Images were captured using SimplePCI software (Compix Inc., Imaging Systems) and were analyzed using ImageJ software (National Institutes of Health).

Techniques: Translocation Assay, Fluorescence, Clinical Proteomics, Membrane, Imaging