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rabbit polyclonal anti laminin primary antibody  (Millipore)

 
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    Structured Review

    Millipore rabbit polyclonal anti laminin primary antibody
    Rabbit Polyclonal Anti Laminin Primary Antibody, supplied by Millipore, 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/rabbit polyclonal anti laminin primary antibody/product/Millipore
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal anti laminin primary antibody - by Bioz Stars, 2025-02
    86/100 stars

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    86
    Millipore rabbit polyclonal anti laminin primary antibody
    Rabbit Polyclonal Anti Laminin Primary Antibody, supplied by Millipore, 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/rabbit polyclonal anti laminin primary antibody/product/Millipore
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal anti laminin primary antibody - by Bioz Stars, 2025-02
    86/100 stars
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    86
    Agilent technologies rabbit polyclonal primary antibody against laminin
    Cross-sections of the OL and GL in the mid-portion of medial recti muscles from a control donor (OL, a1–a3; GL, b1–b3), a spinal-onset ALS donor (OL, c1–c3; GL, d1–d3), and a bulbar-onset ALS donor (OL, e1–e3; GL, f1–f3), triple-labeled for MyHCIIa ( long arrows , green myofibers ), MyHCI ( arrowheads , red myofibers ), and <t>laminin</t> ( gray ), which labels the basal lamina, thereby delineating the myofiber contours as well as making nerve fascicles and capillaries visible. A proportion of the myofibers was not labeled with either antibody and was inferred to contain MyHCeom ( short arrows ). The labeling of myofibers containing MyHCIIa was more homogeneous and stronger in the GL of the control donors (b1, b3) compared to the GL in both spinal-onset ALS donors (d1, d3) and bulbar-onset ALS donors (f1, f3). The labeling intensity of myofibers containing MyHCIIa was less heterogeneous in the OL of control donors (a1, a3) than both spinal-onset ALS donors (c1, c3) and bulbar-onset donors (e1, e3). Myofibers that were not labeled with antibodies against either MyHCIIa or MyHCI were more frequent in the GL of the spinal-onset ALS donors (d3) and even more abundant in the bulbar-onset ALS donors (f3) compared to the myofibers in the GL of control donors (b3). Scale bar : 50 µm.
    Rabbit Polyclonal Primary Antibody Against Laminin, supplied by Agilent technologies, 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/rabbit polyclonal primary antibody against laminin/product/Agilent technologies
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal primary antibody against laminin - by Bioz Stars, 2025-02
    86/100 stars
      Buy from Supplier

    86
    Millipore primary) rabbit polyclonal anti-laminin antibody (diluted
    Cross-sections of the OL and GL in the mid-portion of medial recti muscles from a control donor (OL, a1–a3; GL, b1–b3), a spinal-onset ALS donor (OL, c1–c3; GL, d1–d3), and a bulbar-onset ALS donor (OL, e1–e3; GL, f1–f3), triple-labeled for MyHCIIa ( long arrows , green myofibers ), MyHCI ( arrowheads , red myofibers ), and <t>laminin</t> ( gray ), which labels the basal lamina, thereby delineating the myofiber contours as well as making nerve fascicles and capillaries visible. A proportion of the myofibers was not labeled with either antibody and was inferred to contain MyHCeom ( short arrows ). The labeling of myofibers containing MyHCIIa was more homogeneous and stronger in the GL of the control donors (b1, b3) compared to the GL in both spinal-onset ALS donors (d1, d3) and bulbar-onset ALS donors (f1, f3). The labeling intensity of myofibers containing MyHCIIa was less heterogeneous in the OL of control donors (a1, a3) than both spinal-onset ALS donors (c1, c3) and bulbar-onset donors (e1, e3). Myofibers that were not labeled with antibodies against either MyHCIIa or MyHCI were more frequent in the GL of the spinal-onset ALS donors (d3) and even more abundant in the bulbar-onset ALS donors (f3) compared to the myofibers in the GL of control donors (b3). Scale bar : 50 µm.
    Primary) Rabbit Polyclonal Anti Laminin Antibody (Diluted, supplied by Millipore, 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/primary) rabbit polyclonal anti-laminin antibody (diluted/product/Millipore
    Average 86 stars, based on 1 article reviews
    primary) rabbit polyclonal anti-laminin antibody (diluted - by Bioz Stars, 2025-02
    86/100 stars
      Buy from Supplier

    86
    Millipore primary rabbit polyclonal anti laminin antibody
    Extravasation of biodegradable microspheres at D14. (A) Examples of biodegradable microspheres (white in overlay) scored as ‘in’, ‘going out’ and ‘out’ in coronal brain sections stained by i.v. injected lectin (red) before killing, and postmortem for <t>laminin</t> (green). Scale bar = 25 µm. (B) Quantification of microsphere extravasation of M1 (black), M2 (red), and M3 (green) microspheres at D14. (C) An extravasation score between 0 and 2 was calculated per rat (‘in’ was weighed as 0, ‘going out’ as 1 and ‘out’ as 2). (B) and (C) M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the extravasation analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. * P < 0.05, ** P < 0.01, Kruskal-Wallis with Dunn’s multiple comparison test.
    Primary Rabbit Polyclonal Anti Laminin Antibody, supplied by Millipore, 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/primary rabbit polyclonal anti laminin antibody/product/Millipore
    Average 86 stars, based on 1 article reviews
    primary rabbit polyclonal anti laminin antibody - by Bioz Stars, 2025-02
    86/100 stars
      Buy from Supplier

    86
    Millipore rabbit anti laminin primary polyclonal antibody
    Extravasation of biodegradable microspheres at D14. (A) Examples of biodegradable microspheres (white in overlay) scored as ‘in’, ‘going out’ and ‘out’ in coronal brain sections stained by i.v. injected lectin (red) before killing, and postmortem for <t>laminin</t> (green). Scale bar = 25 µm. (B) Quantification of microsphere extravasation of M1 (black), M2 (red), and M3 (green) microspheres at D14. (C) An extravasation score between 0 and 2 was calculated per rat (‘in’ was weighed as 0, ‘going out’ as 1 and ‘out’ as 2). (B) and (C) M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the extravasation analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. * P < 0.05, ** P < 0.01, Kruskal-Wallis with Dunn’s multiple comparison test.
    Rabbit Anti Laminin Primary Polyclonal Antibody, supplied by Millipore, 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/rabbit anti laminin primary polyclonal antibody/product/Millipore
    Average 86 stars, based on 1 article reviews
    rabbit anti laminin primary polyclonal antibody - by Bioz Stars, 2025-02
    86/100 stars
      Buy from Supplier

    86
    Millipore rabbit anti mouse laminin polyclonal primary antibody
    Extravasation of biodegradable microspheres at D14. (A) Examples of biodegradable microspheres (white in overlay) scored as ‘in’, ‘going out’ and ‘out’ in coronal brain sections stained by i.v. injected lectin (red) before killing, and postmortem for <t>laminin</t> (green). Scale bar = 25 µm. (B) Quantification of microsphere extravasation of M1 (black), M2 (red), and M3 (green) microspheres at D14. (C) An extravasation score between 0 and 2 was calculated per rat (‘in’ was weighed as 0, ‘going out’ as 1 and ‘out’ as 2). (B) and (C) M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the extravasation analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. * P < 0.05, ** P < 0.01, Kruskal-Wallis with Dunn’s multiple comparison test.
    Rabbit Anti Mouse Laminin Polyclonal Primary Antibody, supplied by Millipore, 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/rabbit anti mouse laminin polyclonal primary antibody/product/Millipore
    Average 86 stars, based on 1 article reviews
    rabbit anti mouse laminin polyclonal primary antibody - by Bioz Stars, 2025-02
    86/100 stars
      Buy from Supplier

    Image Search Results


    Cross-sections of the OL and GL in the mid-portion of medial recti muscles from a control donor (OL, a1–a3; GL, b1–b3), a spinal-onset ALS donor (OL, c1–c3; GL, d1–d3), and a bulbar-onset ALS donor (OL, e1–e3; GL, f1–f3), triple-labeled for MyHCIIa ( long arrows , green myofibers ), MyHCI ( arrowheads , red myofibers ), and laminin ( gray ), which labels the basal lamina, thereby delineating the myofiber contours as well as making nerve fascicles and capillaries visible. A proportion of the myofibers was not labeled with either antibody and was inferred to contain MyHCeom ( short arrows ). The labeling of myofibers containing MyHCIIa was more homogeneous and stronger in the GL of the control donors (b1, b3) compared to the GL in both spinal-onset ALS donors (d1, d3) and bulbar-onset ALS donors (f1, f3). The labeling intensity of myofibers containing MyHCIIa was less heterogeneous in the OL of control donors (a1, a3) than both spinal-onset ALS donors (c1, c3) and bulbar-onset donors (e1, e3). Myofibers that were not labeled with antibodies against either MyHCIIa or MyHCI were more frequent in the GL of the spinal-onset ALS donors (d3) and even more abundant in the bulbar-onset ALS donors (f3) compared to the myofibers in the GL of control donors (b3). Scale bar : 50 µm.

    Journal: Investigative Ophthalmology & Visual Science

    Article Title: Myofiber Type Shift in Extraocular Muscles in Amyotrophic Lateral Sclerosis

    doi: 10.1167/iovs.64.5.15

    Figure Lengend Snippet: Cross-sections of the OL and GL in the mid-portion of medial recti muscles from a control donor (OL, a1–a3; GL, b1–b3), a spinal-onset ALS donor (OL, c1–c3; GL, d1–d3), and a bulbar-onset ALS donor (OL, e1–e3; GL, f1–f3), triple-labeled for MyHCIIa ( long arrows , green myofibers ), MyHCI ( arrowheads , red myofibers ), and laminin ( gray ), which labels the basal lamina, thereby delineating the myofiber contours as well as making nerve fascicles and capillaries visible. A proportion of the myofibers was not labeled with either antibody and was inferred to contain MyHCeom ( short arrows ). The labeling of myofibers containing MyHCIIa was more homogeneous and stronger in the GL of the control donors (b1, b3) compared to the GL in both spinal-onset ALS donors (d1, d3) and bulbar-onset ALS donors (f1, f3). The labeling intensity of myofibers containing MyHCIIa was less heterogeneous in the OL of control donors (a1, a3) than both spinal-onset ALS donors (c1, c3) and bulbar-onset donors (e1, e3). Myofibers that were not labeled with antibodies against either MyHCIIa or MyHCI were more frequent in the GL of the spinal-onset ALS donors (d3) and even more abundant in the bulbar-onset ALS donors (f3) compared to the myofibers in the GL of control donors (b3). Scale bar : 50 µm.

    Article Snippet: Rabbit polyclonal primary antibody against laminin was used to label myofiber contours (Z 0097; Dako Denmark A/S, Glostrup, Denmark).

    Techniques: Muscles, Control, Labeling

    Extravasation of biodegradable microspheres at D14. (A) Examples of biodegradable microspheres (white in overlay) scored as ‘in’, ‘going out’ and ‘out’ in coronal brain sections stained by i.v. injected lectin (red) before killing, and postmortem for laminin (green). Scale bar = 25 µm. (B) Quantification of microsphere extravasation of M1 (black), M2 (red), and M3 (green) microspheres at D14. (C) An extravasation score between 0 and 2 was calculated per rat (‘in’ was weighed as 0, ‘going out’ as 1 and ‘out’ as 2). (B) and (C) M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the extravasation analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. * P < 0.05, ** P < 0.01, Kruskal-Wallis with Dunn’s multiple comparison test.

    Journal: Drug Delivery

    Article Title: Extravasation of biodegradable microspheres in the rat brain

    doi: 10.1080/10717544.2023.2194579

    Figure Lengend Snippet: Extravasation of biodegradable microspheres at D14. (A) Examples of biodegradable microspheres (white in overlay) scored as ‘in’, ‘going out’ and ‘out’ in coronal brain sections stained by i.v. injected lectin (red) before killing, and postmortem for laminin (green). Scale bar = 25 µm. (B) Quantification of microsphere extravasation of M1 (black), M2 (red), and M3 (green) microspheres at D14. (C) An extravasation score between 0 and 2 was calculated per rat (‘in’ was weighed as 0, ‘going out’ as 1 and ‘out’ as 2). (B) and (C) M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the extravasation analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. * P < 0.05, ** P < 0.01, Kruskal-Wallis with Dunn’s multiple comparison test.

    Article Snippet: The following antibodies were used: (primary) rabbit polyclonal anti-laminin antibody (diluted 1:500, Cat #L9393; Sigma-Aldrich, Zwijndrecht, The Netherlands), rabbit polyclonal anti-Iba 1 antibody (diluted 1:1000, Cat #019-19741, Wako, Neuss, Germany), mouse anti-NeuN antibody (NEUronal Nuclei, clone A60; diluted 1:200, Cat #MAB377, Millipore BV, Amsterdam, The Netherlands), and (secondary) goat-anti-mouse Cy5 (diluted 1:500) or goat-anti-rabbit Cy5; diluted 1:200) diluted in blocking buffer.

    Techniques: Staining, Injection

    Perfused vessels after microembolization with biodegradable microspheres at D14. (A) Examples of vessels obstructed with biodegradable microspheres. Top panel shows a nonperfused vessel, indicated by lack of i.v. lectin perfusion (red; indicated by asterisks) proximally and distally of the microsphere (white), while the vessel wall is clearly outlined by laminin (green). Bottom panel shows a perfused vessel, despite the presence of a microsphere. Scale bar = 25 µm. (B) Quantification of vessel perfusion after microembolization with M1 (black), M2 (red), and M3 (green) microspheres at D14. M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the perfusion analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. ** P < 0.01, ANOVA with Tukey’s multiple comparison test.

    Journal: Drug Delivery

    Article Title: Extravasation of biodegradable microspheres in the rat brain

    doi: 10.1080/10717544.2023.2194579

    Figure Lengend Snippet: Perfused vessels after microembolization with biodegradable microspheres at D14. (A) Examples of vessels obstructed with biodegradable microspheres. Top panel shows a nonperfused vessel, indicated by lack of i.v. lectin perfusion (red; indicated by asterisks) proximally and distally of the microsphere (white), while the vessel wall is clearly outlined by laminin (green). Bottom panel shows a perfused vessel, despite the presence of a microsphere. Scale bar = 25 µm. (B) Quantification of vessel perfusion after microembolization with M1 (black), M2 (red), and M3 (green) microspheres at D14. M1: n = 6, M2: n = 7, M3: n = 7 animals (one M2 animal was excluded from the perfusion analysis because the i.v. lectin injection failed). Data are depicted as median ± IQR (box) and min – max (whiskers), each data point represents an individual animal. ** P < 0.01, ANOVA with Tukey’s multiple comparison test.

    Article Snippet: The following antibodies were used: (primary) rabbit polyclonal anti-laminin antibody (diluted 1:500, Cat #L9393; Sigma-Aldrich, Zwijndrecht, The Netherlands), rabbit polyclonal anti-Iba 1 antibody (diluted 1:1000, Cat #019-19741, Wako, Neuss, Germany), mouse anti-NeuN antibody (NEUronal Nuclei, clone A60; diluted 1:200, Cat #MAB377, Millipore BV, Amsterdam, The Netherlands), and (secondary) goat-anti-mouse Cy5 (diluted 1:500) or goat-anti-rabbit Cy5; diluted 1:200) diluted in blocking buffer.

    Techniques: Injection