dylight 488 lycopersicon esculentum tomato  (Vector Laboratories)


Bioz Verified Symbol Vector Laboratories is a verified supplier
Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories dylight 488 lycopersicon esculentum tomato
    Dylight 488 Lycopersicon Esculentum Tomato, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dylight 488 lycopersicon esculentum tomato/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    dylight 488 lycopersicon esculentum tomato - by Bioz Stars, 2024-06
    86/100 stars

    Images

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with <t>lectin</t> to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function"

    Article Title: Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function

    Journal: Brain

    doi: 10.1093/brain/awae065

    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Figure Legend Snippet: Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.

    Techniques Used: Slice Preparation, Immunostaining, Fluorescence, Expressing, Staining, Generated

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with <t>lectin</t> to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function"

    Article Title: Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function

    Journal: Brain

    doi: 10.1093/brain/awae065

    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Figure Legend Snippet: Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.

    Techniques Used: Slice Preparation, Immunostaining, Fluorescence, Expressing, Staining, Generated

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with <t>lectin</t> to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function"

    Article Title: Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function

    Journal: Brain

    doi: 10.1093/brain/awae065

    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Figure Legend Snippet: Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.

    Techniques Used: Slice Preparation, Immunostaining, Fluorescence, Expressing, Staining, Generated

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin

    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "CCR2 + monocytes replenish border-associated macrophages in the diseased mouse brain"

    Article Title: CCR2 + monocytes replenish border-associated macrophages in the diseased mouse brain

    Journal: Cell reports

    doi: 10.1016/j.celrep.2024.114120


    Figure Legend Snippet:

    Techniques Used: Recombinant, Plasmid Preparation, Software, Microscopy, Flow Cytometry

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    20 h of delipidation is sufficient to clear most young adult mouse tissues Lightsheet images of the eye (A), kidney (B), heart (C) testes (D) and brain (E) from 2 month old mice perfused with far-red fluorescent <t>lectin</t> to label the vascular endothelium after 20 h of delipidation (using 50% THF) and RI matching in EZ View. Numbers below correspond to white boxed in regions in the above images. Successful clearing and lightsheet imaging should yield images where smaller blood vessels are clearly resolved, as shown in the bottom panels of the figure. Scale bars in A1, B1 = 400 μm; C1 = 500 μm; A2 = 140 μm; B2, C2 = 200 μm; D1 = 400 μm; E1 = 1500 μm; D2 = 100 μm; E2 = 500 μm.
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "Protocol for optical, aqueous-based clearing of murine tissues using EZ Clear"

    Article Title: Protocol for optical, aqueous-based clearing of murine tissues using EZ Clear

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2024.103053

    20 h of delipidation is sufficient to clear most young adult mouse tissues Lightsheet images of the eye (A), kidney (B), heart (C) testes (D) and brain (E) from 2 month old mice perfused with far-red fluorescent lectin to label the vascular endothelium after 20 h of delipidation (using 50% THF) and RI matching in EZ View. Numbers below correspond to white boxed in regions in the above images. Successful clearing and lightsheet imaging should yield images where smaller blood vessels are clearly resolved, as shown in the bottom panels of the figure. Scale bars in A1, B1 = 400 μm; C1 = 500 μm; A2 = 140 μm; B2, C2 = 200 μm; D1 = 400 μm; E1 = 1500 μm; D2 = 100 μm; E2 = 500 μm.
    Figure Legend Snippet: 20 h of delipidation is sufficient to clear most young adult mouse tissues Lightsheet images of the eye (A), kidney (B), heart (C) testes (D) and brain (E) from 2 month old mice perfused with far-red fluorescent lectin to label the vascular endothelium after 20 h of delipidation (using 50% THF) and RI matching in EZ View. Numbers below correspond to white boxed in regions in the above images. Successful clearing and lightsheet imaging should yield images where smaller blood vessels are clearly resolved, as shown in the bottom panels of the figure. Scale bars in A1, B1 = 400 μm; C1 = 500 μm; A2 = 140 μm; B2, C2 = 200 μm; D1 = 400 μm; E1 = 1500 μm; D2 = 100 μm; E2 = 500 μm.

    Techniques Used: Imaging

    Increasing delipidation time from 20 h to 68 h dramatically improves tissue clearing and imaging in aged adult mouse tissues Lightsheet images of kidney (A and B), heart (C and D), ovary (E), eye (F) and spleen (G) from 5 month old mice following perfusion with far red fluorescent lectin to label blood vessels. Kidney and heart samples were delipidated for 20 h (A and C) and then imaged following RI matching. These exact same tissues were then subjected to an additional 48 h of delipidation prior to a second round of RI matching and imaging (B and D). The kidney sample delipidated for 20 h (A) does not show any discernable vasculature, indicating that this incubation time is not adequate for tissue clearing of 5 month old kidney. After an additional 48 h of delipidation, the vasculature of the 5 month old kidney (B) is evident. The heart after 20 h of delipidation (C) shows clear signal in the vasculature, although some areas lack crisp signal. However, an additional 48 h of delipidation adds detail previously undetected with the 20 h delipidation and improves the signal to noise ratio. 20 h of delipidation is adequate for the ovary (E) and eye (F), whereas the spleen requires an additional 48 h of delipidation to observe optimal signal. Scale bars in A1–D1 = 500 μm; A2–E1 = 200 μm; F1 = 300 μm; G1 = 700 μm; E2 = 70 μm; F2 = 100 μm; G2 = 200 μm.
    Figure Legend Snippet: Increasing delipidation time from 20 h to 68 h dramatically improves tissue clearing and imaging in aged adult mouse tissues Lightsheet images of kidney (A and B), heart (C and D), ovary (E), eye (F) and spleen (G) from 5 month old mice following perfusion with far red fluorescent lectin to label blood vessels. Kidney and heart samples were delipidated for 20 h (A and C) and then imaged following RI matching. These exact same tissues were then subjected to an additional 48 h of delipidation prior to a second round of RI matching and imaging (B and D). The kidney sample delipidated for 20 h (A) does not show any discernable vasculature, indicating that this incubation time is not adequate for tissue clearing of 5 month old kidney. After an additional 48 h of delipidation, the vasculature of the 5 month old kidney (B) is evident. The heart after 20 h of delipidation (C) shows clear signal in the vasculature, although some areas lack crisp signal. However, an additional 48 h of delipidation adds detail previously undetected with the 20 h delipidation and improves the signal to noise ratio. 20 h of delipidation is adequate for the ovary (E) and eye (F), whereas the spleen requires an additional 48 h of delipidation to observe optimal signal. Scale bars in A1–D1 = 500 μm; A2–E1 = 200 μm; F1 = 300 μm; G1 = 700 μm; E2 = 70 μm; F2 = 100 μm; G2 = 200 μm.

    Techniques Used: Imaging, Incubation


    Figure Legend Snippet:

    Techniques Used: Recombinant, Saline, Plasmid Preparation, Dissection, Suction Filtration, Pore Size, Fluorescence, Microscopy

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    20 h of delipidation is sufficient to clear most young adult mouse tissues Lightsheet images of the eye (A), kidney (B), heart (C) testes (D) and brain (E) from 2 month old mice perfused with far-red fluorescent <t>lectin</t> to label the vascular endothelium after 20 h of delipidation (using 50% THF) and RI matching in EZ View. Numbers below correspond to white boxed in regions in the above images. Successful clearing and lightsheet imaging should yield images where smaller blood vessels are clearly resolved, as shown in the bottom panels of the figure. Scale bars in A1, B1 = 400 μm; C1 = 500 μm; A2 = 140 μm; B2, C2 = 200 μm; D1 = 400 μm; E1 = 1500 μm; D2 = 100 μm; E2 = 500 μm.
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    1) Product Images from "Protocol for optical, aqueous-based clearing of murine tissues using EZ Clear"

    Article Title: Protocol for optical, aqueous-based clearing of murine tissues using EZ Clear

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2024.103053

    20 h of delipidation is sufficient to clear most young adult mouse tissues Lightsheet images of the eye (A), kidney (B), heart (C) testes (D) and brain (E) from 2 month old mice perfused with far-red fluorescent lectin to label the vascular endothelium after 20 h of delipidation (using 50% THF) and RI matching in EZ View. Numbers below correspond to white boxed in regions in the above images. Successful clearing and lightsheet imaging should yield images where smaller blood vessels are clearly resolved, as shown in the bottom panels of the figure. Scale bars in A1, B1 = 400 μm; C1 = 500 μm; A2 = 140 μm; B2, C2 = 200 μm; D1 = 400 μm; E1 = 1500 μm; D2 = 100 μm; E2 = 500 μm.
    Figure Legend Snippet: 20 h of delipidation is sufficient to clear most young adult mouse tissues Lightsheet images of the eye (A), kidney (B), heart (C) testes (D) and brain (E) from 2 month old mice perfused with far-red fluorescent lectin to label the vascular endothelium after 20 h of delipidation (using 50% THF) and RI matching in EZ View. Numbers below correspond to white boxed in regions in the above images. Successful clearing and lightsheet imaging should yield images where smaller blood vessels are clearly resolved, as shown in the bottom panels of the figure. Scale bars in A1, B1 = 400 μm; C1 = 500 μm; A2 = 140 μm; B2, C2 = 200 μm; D1 = 400 μm; E1 = 1500 μm; D2 = 100 μm; E2 = 500 μm.

    Techniques Used: Imaging

    Increasing delipidation time from 20 h to 68 h dramatically improves tissue clearing and imaging in aged adult mouse tissues Lightsheet images of kidney (A and B), heart (C and D), ovary (E), eye (F) and spleen (G) from 5 month old mice following perfusion with far red fluorescent lectin to label blood vessels. Kidney and heart samples were delipidated for 20 h (A and C) and then imaged following RI matching. These exact same tissues were then subjected to an additional 48 h of delipidation prior to a second round of RI matching and imaging (B and D). The kidney sample delipidated for 20 h (A) does not show any discernable vasculature, indicating that this incubation time is not adequate for tissue clearing of 5 month old kidney. After an additional 48 h of delipidation, the vasculature of the 5 month old kidney (B) is evident. The heart after 20 h of delipidation (C) shows clear signal in the vasculature, although some areas lack crisp signal. However, an additional 48 h of delipidation adds detail previously undetected with the 20 h delipidation and improves the signal to noise ratio. 20 h of delipidation is adequate for the ovary (E) and eye (F), whereas the spleen requires an additional 48 h of delipidation to observe optimal signal. Scale bars in A1–D1 = 500 μm; A2–E1 = 200 μm; F1 = 300 μm; G1 = 700 μm; E2 = 70 μm; F2 = 100 μm; G2 = 200 μm.
    Figure Legend Snippet: Increasing delipidation time from 20 h to 68 h dramatically improves tissue clearing and imaging in aged adult mouse tissues Lightsheet images of kidney (A and B), heart (C and D), ovary (E), eye (F) and spleen (G) from 5 month old mice following perfusion with far red fluorescent lectin to label blood vessels. Kidney and heart samples were delipidated for 20 h (A and C) and then imaged following RI matching. These exact same tissues were then subjected to an additional 48 h of delipidation prior to a second round of RI matching and imaging (B and D). The kidney sample delipidated for 20 h (A) does not show any discernable vasculature, indicating that this incubation time is not adequate for tissue clearing of 5 month old kidney. After an additional 48 h of delipidation, the vasculature of the 5 month old kidney (B) is evident. The heart after 20 h of delipidation (C) shows clear signal in the vasculature, although some areas lack crisp signal. However, an additional 48 h of delipidation adds detail previously undetected with the 20 h delipidation and improves the signal to noise ratio. 20 h of delipidation is adequate for the ovary (E) and eye (F), whereas the spleen requires an additional 48 h of delipidation to observe optimal signal. Scale bars in A1–D1 = 500 μm; A2–E1 = 200 μm; F1 = 300 μm; G1 = 700 μm; E2 = 70 μm; F2 = 100 μm; G2 = 200 μm.

    Techniques Used: Imaging, Incubation


    Figure Legend Snippet:

    Techniques Used: Recombinant, Saline, Plasmid Preparation, Dissection, Suction Filtration, Pore Size, Fluorescence, Microscopy

    lycopersicon esculentum tomato lectin  (Vector Laboratories)


    Bioz Verified Symbol Vector Laboratories is a verified supplier
    Bioz Manufacturer Symbol Vector Laboratories manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Vector Laboratories lycopersicon esculentum tomato lectin
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars

    Images

    Similar Products

  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86
    Vector Laboratories dylight 488 lycopersicon esculentum tomato
    Dylight 488 Lycopersicon Esculentum Tomato, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dylight 488 lycopersicon esculentum tomato/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    dylight 488 lycopersicon esculentum tomato - by Bioz Stars, 2024-06
    86/100 stars
      Buy from Supplier

    86
    Vector Laboratories lycopersicon esculentum tomato lectin
    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with <t>lectin</t> to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.
    Lycopersicon Esculentum Tomato Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lycopersicon esculentum tomato lectin/product/Vector Laboratories
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    lycopersicon esculentum tomato lectin - by Bioz Stars, 2024-06
    86/100 stars
      Buy from Supplier

    Image Search Results


    Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.

    Journal: Brain

    Article Title: Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function

    doi: 10.1093/brain/awae065

    Figure Lengend Snippet: Increased AQP4 in the murine brain following mild repetitive blast traumatic brain injury. (A) Representative whole brain slice images of AQP4 immunostaining in mouse brains of Sham group and 7 (7D Blast) and 28 days (28D Blast) post mild repetitive blast traumatic brain injury (mTBI). (B) Representative dorsal cortex images of AQP4 immunostaining in Sham, 7D Blast and 28D Blast mouse brains. Scale bar = 200 μm. Increased AQP4, particularly at the cortical surface, was observed at 28 days post mTBI. (C) Representative images of the regions of interest drawn for regional shell analysis of AQP4 in outer grey, inner grey and white matter and representative dorsal and ventral lines drawn for AQP4 line analysis generate intensity plots of AQP4 across the tissue. (D) AQP4 fluorescence intensity from regional shell analysis showing AQP4 immunoreactivity was significantly increased in the outer grey matter at 28 days post mTBI. Data are mean ± SEM from n = 8–10 per group and were analysed with two-way repeated measure ANOVA followed by Sidak’s post hoc test (*P < 0.05, 28 days versus 7 days post mTBI; *P < 0.05, 28 days post mTBI versus Sham). (E) Averaged fluorescence intensity plots from the dorsal surface through the grey matter (as shown in D) and into the subcortical white matter. Data are mean ± SEM from n = 9–10 mice/group. (F) Averaged fluorescence intensity plots extending from the ventral surface through the grey matter (as shown in D) for n = 9 per group. (G) Quantification of AQP4 expression and localization in the dorsal cortex. AQP4 was co-stained with lectin to label blood vessels, a vessel mask was generated and AQP4 fluorescence intensity was measured inside or outside the vessel mask to quantify perivascular (PV) and non-PV AQP4, respectively. AQP4 ratios were calculated as PV/non-PV. (H) Quantification and localization of AQP4 in the ventral cortex. Data were analysed with two-sided t-test. GM = grey matter; WM = white matter.

    Article Snippet: Following overnight primary incubation, sections were incubated with secondary antibodies donkey anti-rabbit Alexa Fluor 647 (1:500; Invitrogen, Cat. No. #A21207) and DyLight 488-labelled Lycopersicon esculentum (Tomato) lectin (Vector Labs, Cat. No. #DL-1177) or donkey anti-mouse Alexa Fluor 488 (1:250; Invitrogen, Cat. No. #A21202) for 2 h at room temperature.

    Techniques: Slice Preparation, Immunostaining, Fluorescence, Expressing, Staining, Generated