simplepci software 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, 2026-05
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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, 2026-05
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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, 2026-05
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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
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simplepci 6.0 software - by Bioz Stars, 2026-05
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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, 2026-05
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hamamatsu simplepci software  (Hamamatsu)
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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, 2026-05
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digital imaging software simplepci 5a  (Compix Inc)
90
Compix Inc digital imaging software simplepci 5a
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.
Digital Imaging Software Simplepci 5a, 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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digital imaging software simplepci 5a - by Bioz Stars, 2026-05
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image analysis simple pci  (Hamamatsu)
90
Hamamatsu image analysis simple pci
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.
Image Analysis Simple Pci, 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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computer software simplepci  (Compix Inc)
90
Compix Inc computer software 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.
Computer Software 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/computer software simplepci/product/Compix Inc
Average 90 stars, based on 1 article reviews
computer software simplepci - by Bioz Stars, 2026-05
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simplepci acquisition software  (Hamamatsu)
90
Hamamatsu simplepci acquisition 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 Acquisition 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 acquisition software/product/Hamamatsu
Average 90 stars, based on 1 article reviews
simplepci acquisition software - by Bioz Stars, 2026-05
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simplepci aic software  (Compix Inc)
90
Compix Inc simplepci aic 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 Aic 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 aic software/product/Compix Inc
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simplepci 5.3.1 software  (Hamamatsu)
90
Hamamatsu simplepci 5.3.1 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 5.3.1 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
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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