single precision float (32-bit) Search Results


90
STMicroelectronics Pte mcu stm32f429
Mcu Stm32f429, supplied by STMicroelectronics Pte, 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/product/single+precision+float+%2832-bit%29/pmc04118367-53-80-87?v=STMicroelectronics+Pte
Average 90 stars, based on 1 article reviews
mcu stm32f429 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
STMicroelectronics Pte stm32l 32-bit ultra-low power arm-based microprocessor
Stm32l 32 Bit Ultra Low Power Arm Based Microprocessor, supplied by STMicroelectronics Pte, 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/product/single+precision+float+%2832-bit%29/us11885838-319-14-22?v=STMicroelectronics+Pte
Average 90 stars, based on 1 article reviews
stm32l 32-bit ultra-low power arm-based microprocessor - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
STMicroelectronics Pte 32-bit microcontroller unit
32 Bit Microcontroller Unit, supplied by STMicroelectronics Pte, 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/product/single+precision+float+%2832-bit%29/us11925792-62-10-9?v=STMicroelectronics+Pte
Average 90 stars, based on 1 article reviews
32-bit microcontroller unit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
Silicon Laboratories Inc the efm32 tiny gecko 32-bit microcontroller
The Efm32 Tiny Gecko 32 Bit Microcontroller, supplied by Silicon Laboratories 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/product/single+precision+float+%2832-bit%29/us11445965-552-18-25?v=Silicon+Laboratories+Inc
Average 90 stars, based on 1 article reviews
the efm32 tiny gecko 32-bit microcontroller - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
Carl Zeiss axiovision (release 4.8.2 sp3, 32-bit)
Axiovision (Release 4.8.2 Sp3, 32 Bit), supplied by Carl Zeiss, 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/product/single+precision+float+%2832-bit%29/pmc09909437-297-15-9?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
axiovision (release 4.8.2 sp3, 32-bit) - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
MBF Bioscience image analysis software neurolucida® 9.14.5 32 bit
Image Analysis Software Neurolucida® 9.14.5 32 Bit, supplied by MBF Bioscience, 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/product/single+precision+float+%2832-bit%29/pmc06151128-51-12-19?v=MBF+Bioscience
Average 90 stars, based on 1 article reviews
image analysis software neurolucida® 9.14.5 32 bit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
Anwendung GmbH 16- und 32-bit
16 Und 32 Bit, supplied by Anwendung GmbH, 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/product/single+precision+float+%2832-bit%29/10__1002_slash_phbl__19960521103-346-15-17?v=Anwendung+GmbH
Average 90 stars, based on 1 article reviews
16- und 32-bit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
SAS institute version 9.4, 32-bit
Version 9.4, 32 Bit, supplied by SAS institute, 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/product/single+precision+float+%2832-bit%29/pmc08244318-177-8-9?v=SAS+institute
Average 90 stars, based on 1 article reviews
version 9.4, 32-bit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
STMicroelectronics Pte enhanced st20 32-bit vl-risc
Enhanced St20 32 Bit Vl Risc, supplied by STMicroelectronics Pte, 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/product/single+precision+float+%2832-bit%29/us09866789-133-8-7?v=STMicroelectronics+Pte
Average 90 stars, based on 1 article reviews
enhanced st20 32-bit vl-risc - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
MBF Bioscience stereological image analysis software neurolucida® 9.14.5 32 bit
a, Schematics show demarcation of SCI lesion center (Cn) and evenly spaced lines beyond the Cn placed by <t>image</t> <t>analysis</t> <t>software</t> (Neurolucida®, Microbrightfield) for quantification of axon intercepts in horizontal tissue sections of mice with SCI and one (D 1 ) or two (D 1 +D 2 ) hydrogel depots. b, Multi-fluorescent, survey images show BDA-labeled axons and GFAP-labelled astrocytes that demarcate astrocyte scar proximal borders (PB) and distal borders (DB) around the non-neural lesion core (LC) after SCI. The hydrogel of the empty depot (left) was tagged with a blue fluorescent label for visualization. Note the essential absence of axons passing the astrocyte scar (AS) proximal border (PB) to reach the lesion center (Cn) or beyond in the mouse with SCI plus empty depot (left), in striking contrast with the large number of axons that regrew through the lesion core (LC) and passed beyond the distal astrocyte scar border (DB) into spared grey matter (gm) in the mouse with full treatment of stimulatory AAV plus growth factors (right). GFAP staining shows that the SCI lesions are anatomically complete across the entire width of the spinal cord in both cases. Note that the second depot was placed at 9 days after SCI, by which time the distal astrocyte scar border was essentially formed . Note also that astrocytes do not migrate into the depots, potentially giving the mistaken impression of cavity formation when looking only at the GFAP channel alone. Nevertheless, examination of other fluorescence channels shows that depot sites clearly contain DAPI-stained stromal cells and BDA-positive axons. c, Large area survey images of BDA-labeled axons in composite mosaic scans of horizontal sections. In a control mouse (top) that received SCI plus empty depot, few axons reach the lesion center, almost none pass beyond, and no axons are present at 3mm. In the a treated mouse (middle) that received stimulatory AAV plus growth factors, many axons regrow through the lesion core and reach or pass 1.5mm beyond the lesion center, which is the equivalent length of a full thoracic spinal segment in mice . Note also that there are no axons present at 3mm, demonstrating that the SCI lesion was complete and that axons that are found past the lesion center represent axon regrowth after SCI in response to the experimental manipulations. In an uninjured mice (bottom), there are many labeled axons at the distance equivalent to 3mm beyond the location of SCI in injured mice. d, Graph shows mean±SEM numbers of axon intercepts at lesion centers for all experimental groups (dots in graphs show numbers and distribution of individual mice per group). (ns not significant versus SCI-only, # P <0.01 versus SCI-only and ns versus each other, ** P <0.01, *** P <0.001 versus all other groups, one-way ANOVA/Bonferroni, F (12, 57) = 22.3).
Stereological Image Analysis Software Neurolucida® 9.14.5 32 Bit, supplied by MBF Bioscience, 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/product/single+precision+float+%2832-bit%29/pmc06151128-62-5-18?v=MBF+Bioscience
Average 90 stars, based on 1 article reviews
stereological image analysis software neurolucida® 9.14.5 32 bit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
Panasonic Healthcare ccd color camera panasonic rgb 32 bit
a, Schematics show demarcation of SCI lesion center (Cn) and evenly spaced lines beyond the Cn placed by <t>image</t> <t>analysis</t> <t>software</t> (Neurolucida®, Microbrightfield) for quantification of axon intercepts in horizontal tissue sections of mice with SCI and one (D 1 ) or two (D 1 +D 2 ) hydrogel depots. b, Multi-fluorescent, survey images show BDA-labeled axons and GFAP-labelled astrocytes that demarcate astrocyte scar proximal borders (PB) and distal borders (DB) around the non-neural lesion core (LC) after SCI. The hydrogel of the empty depot (left) was tagged with a blue fluorescent label for visualization. Note the essential absence of axons passing the astrocyte scar (AS) proximal border (PB) to reach the lesion center (Cn) or beyond in the mouse with SCI plus empty depot (left), in striking contrast with the large number of axons that regrew through the lesion core (LC) and passed beyond the distal astrocyte scar border (DB) into spared grey matter (gm) in the mouse with full treatment of stimulatory AAV plus growth factors (right). GFAP staining shows that the SCI lesions are anatomically complete across the entire width of the spinal cord in both cases. Note that the second depot was placed at 9 days after SCI, by which time the distal astrocyte scar border was essentially formed . Note also that astrocytes do not migrate into the depots, potentially giving the mistaken impression of cavity formation when looking only at the GFAP channel alone. Nevertheless, examination of other fluorescence channels shows that depot sites clearly contain DAPI-stained stromal cells and BDA-positive axons. c, Large area survey images of BDA-labeled axons in composite mosaic scans of horizontal sections. In a control mouse (top) that received SCI plus empty depot, few axons reach the lesion center, almost none pass beyond, and no axons are present at 3mm. In the a treated mouse (middle) that received stimulatory AAV plus growth factors, many axons regrow through the lesion core and reach or pass 1.5mm beyond the lesion center, which is the equivalent length of a full thoracic spinal segment in mice . Note also that there are no axons present at 3mm, demonstrating that the SCI lesion was complete and that axons that are found past the lesion center represent axon regrowth after SCI in response to the experimental manipulations. In an uninjured mice (bottom), there are many labeled axons at the distance equivalent to 3mm beyond the location of SCI in injured mice. d, Graph shows mean±SEM numbers of axon intercepts at lesion centers for all experimental groups (dots in graphs show numbers and distribution of individual mice per group). (ns not significant versus SCI-only, # P <0.01 versus SCI-only and ns versus each other, ** P <0.01, *** P <0.001 versus all other groups, one-way ANOVA/Bonferroni, F (12, 57) = 22.3).
Ccd Color Camera Panasonic Rgb 32 Bit, supplied by Panasonic Healthcare, 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/product/single+precision+float+%2832-bit%29/10__1299_slash_jmmp__4__520-102-1-4?v=Panasonic+Healthcare
Average 90 stars, based on 1 article reviews
ccd color camera panasonic rgb 32 bit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
STMicroelectronics Pte cortex-m4 processor 32-bit stm32f469
a, Schematics show demarcation of SCI lesion center (Cn) and evenly spaced lines beyond the Cn placed by <t>image</t> <t>analysis</t> <t>software</t> (Neurolucida®, Microbrightfield) for quantification of axon intercepts in horizontal tissue sections of mice with SCI and one (D 1 ) or two (D 1 +D 2 ) hydrogel depots. b, Multi-fluorescent, survey images show BDA-labeled axons and GFAP-labelled astrocytes that demarcate astrocyte scar proximal borders (PB) and distal borders (DB) around the non-neural lesion core (LC) after SCI. The hydrogel of the empty depot (left) was tagged with a blue fluorescent label for visualization. Note the essential absence of axons passing the astrocyte scar (AS) proximal border (PB) to reach the lesion center (Cn) or beyond in the mouse with SCI plus empty depot (left), in striking contrast with the large number of axons that regrew through the lesion core (LC) and passed beyond the distal astrocyte scar border (DB) into spared grey matter (gm) in the mouse with full treatment of stimulatory AAV plus growth factors (right). GFAP staining shows that the SCI lesions are anatomically complete across the entire width of the spinal cord in both cases. Note that the second depot was placed at 9 days after SCI, by which time the distal astrocyte scar border was essentially formed . Note also that astrocytes do not migrate into the depots, potentially giving the mistaken impression of cavity formation when looking only at the GFAP channel alone. Nevertheless, examination of other fluorescence channels shows that depot sites clearly contain DAPI-stained stromal cells and BDA-positive axons. c, Large area survey images of BDA-labeled axons in composite mosaic scans of horizontal sections. In a control mouse (top) that received SCI plus empty depot, few axons reach the lesion center, almost none pass beyond, and no axons are present at 3mm. In the a treated mouse (middle) that received stimulatory AAV plus growth factors, many axons regrow through the lesion core and reach or pass 1.5mm beyond the lesion center, which is the equivalent length of a full thoracic spinal segment in mice . Note also that there are no axons present at 3mm, demonstrating that the SCI lesion was complete and that axons that are found past the lesion center represent axon regrowth after SCI in response to the experimental manipulations. In an uninjured mice (bottom), there are many labeled axons at the distance equivalent to 3mm beyond the location of SCI in injured mice. d, Graph shows mean±SEM numbers of axon intercepts at lesion centers for all experimental groups (dots in graphs show numbers and distribution of individual mice per group). (ns not significant versus SCI-only, # P <0.01 versus SCI-only and ns versus each other, ** P <0.01, *** P <0.001 versus all other groups, one-way ANOVA/Bonferroni, F (12, 57) = 22.3).
Cortex M4 Processor 32 Bit Stm32f469, supplied by STMicroelectronics Pte, 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/product/single+precision+float+%2832-bit%29/pm37896739-437-23-25?v=STMicroelectronics+Pte
Average 90 stars, based on 1 article reviews
cortex-m4 processor 32-bit stm32f469 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


a, Schematics show demarcation of SCI lesion center (Cn) and evenly spaced lines beyond the Cn placed by image analysis software (Neurolucida®, Microbrightfield) for quantification of axon intercepts in horizontal tissue sections of mice with SCI and one (D 1 ) or two (D 1 +D 2 ) hydrogel depots. b, Multi-fluorescent, survey images show BDA-labeled axons and GFAP-labelled astrocytes that demarcate astrocyte scar proximal borders (PB) and distal borders (DB) around the non-neural lesion core (LC) after SCI. The hydrogel of the empty depot (left) was tagged with a blue fluorescent label for visualization. Note the essential absence of axons passing the astrocyte scar (AS) proximal border (PB) to reach the lesion center (Cn) or beyond in the mouse with SCI plus empty depot (left), in striking contrast with the large number of axons that regrew through the lesion core (LC) and passed beyond the distal astrocyte scar border (DB) into spared grey matter (gm) in the mouse with full treatment of stimulatory AAV plus growth factors (right). GFAP staining shows that the SCI lesions are anatomically complete across the entire width of the spinal cord in both cases. Note that the second depot was placed at 9 days after SCI, by which time the distal astrocyte scar border was essentially formed . Note also that astrocytes do not migrate into the depots, potentially giving the mistaken impression of cavity formation when looking only at the GFAP channel alone. Nevertheless, examination of other fluorescence channels shows that depot sites clearly contain DAPI-stained stromal cells and BDA-positive axons. c, Large area survey images of BDA-labeled axons in composite mosaic scans of horizontal sections. In a control mouse (top) that received SCI plus empty depot, few axons reach the lesion center, almost none pass beyond, and no axons are present at 3mm. In the a treated mouse (middle) that received stimulatory AAV plus growth factors, many axons regrow through the lesion core and reach or pass 1.5mm beyond the lesion center, which is the equivalent length of a full thoracic spinal segment in mice . Note also that there are no axons present at 3mm, demonstrating that the SCI lesion was complete and that axons that are found past the lesion center represent axon regrowth after SCI in response to the experimental manipulations. In an uninjured mice (bottom), there are many labeled axons at the distance equivalent to 3mm beyond the location of SCI in injured mice. d, Graph shows mean±SEM numbers of axon intercepts at lesion centers for all experimental groups (dots in graphs show numbers and distribution of individual mice per group). (ns not significant versus SCI-only, # P <0.01 versus SCI-only and ns versus each other, ** P <0.01, *** P <0.001 versus all other groups, one-way ANOVA/Bonferroni, F (12, 57) = 22.3).

Journal: Nature

Article Title: Required growth facilitators propel axon regeneration across complete spinal cord injury

doi: 10.1038/s41586-018-0467-6

Figure Lengend Snippet: a, Schematics show demarcation of SCI lesion center (Cn) and evenly spaced lines beyond the Cn placed by image analysis software (Neurolucida®, Microbrightfield) for quantification of axon intercepts in horizontal tissue sections of mice with SCI and one (D 1 ) or two (D 1 +D 2 ) hydrogel depots. b, Multi-fluorescent, survey images show BDA-labeled axons and GFAP-labelled astrocytes that demarcate astrocyte scar proximal borders (PB) and distal borders (DB) around the non-neural lesion core (LC) after SCI. The hydrogel of the empty depot (left) was tagged with a blue fluorescent label for visualization. Note the essential absence of axons passing the astrocyte scar (AS) proximal border (PB) to reach the lesion center (Cn) or beyond in the mouse with SCI plus empty depot (left), in striking contrast with the large number of axons that regrew through the lesion core (LC) and passed beyond the distal astrocyte scar border (DB) into spared grey matter (gm) in the mouse with full treatment of stimulatory AAV plus growth factors (right). GFAP staining shows that the SCI lesions are anatomically complete across the entire width of the spinal cord in both cases. Note that the second depot was placed at 9 days after SCI, by which time the distal astrocyte scar border was essentially formed . Note also that astrocytes do not migrate into the depots, potentially giving the mistaken impression of cavity formation when looking only at the GFAP channel alone. Nevertheless, examination of other fluorescence channels shows that depot sites clearly contain DAPI-stained stromal cells and BDA-positive axons. c, Large area survey images of BDA-labeled axons in composite mosaic scans of horizontal sections. In a control mouse (top) that received SCI plus empty depot, few axons reach the lesion center, almost none pass beyond, and no axons are present at 3mm. In the a treated mouse (middle) that received stimulatory AAV plus growth factors, many axons regrow through the lesion core and reach or pass 1.5mm beyond the lesion center, which is the equivalent length of a full thoracic spinal segment in mice . Note also that there are no axons present at 3mm, demonstrating that the SCI lesion was complete and that axons that are found past the lesion center represent axon regrowth after SCI in response to the experimental manipulations. In an uninjured mice (bottom), there are many labeled axons at the distance equivalent to 3mm beyond the location of SCI in injured mice. d, Graph shows mean±SEM numbers of axon intercepts at lesion centers for all experimental groups (dots in graphs show numbers and distribution of individual mice per group). (ns not significant versus SCI-only, # P <0.01 versus SCI-only and ns versus each other, ** P <0.01, *** P <0.001 versus all other groups, one-way ANOVA/Bonferroni, F (12, 57) = 22.3).

Article Snippet: Cell counts were performed using stereological image analysis software (StereoInvestigator®, 9.14.5 32 Bit, and NeuroLucida®, 9.14.5 32 Bit, MicroBrightField, Williston, VT) operating a computer-driven microscope regulated in the x, y and z axes (Zeiss).

Techniques: Software, Labeling, Staining, Fluorescence, Control