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mouse anti-leuenkephalin  (BioIVT Inc)

 
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    BioIVT Inc mouse anti-leuenkephalin
    Characterization of α2A-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2A-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U) depicts α2A-AR-IR (red). The second column (B, F, J,N, R, V) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column(C, G, K,O, S, W) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column(D, H, L,P, T, X) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2A-AR -IR and α2C-AR-IR are rarely colocalized. Row 2(E–H) demonstrates that α2A-AR-IR and SP-IR are highly colocalized. Row 3 (I–L) demonstrates that α2A-AR-IR and CGRP-IR fibers are highly, but not exclusively, colocalized. Row 4(M–P) demonstrates that α2A-AR-IR and ENK-IR are rarely colocalized. Row 5 (Q–T) demonstrates that α2A-AR-IR and DβH-IR are closely apposed, but not colocalized. Similarly, row 6(U–X) demonstrates that instances of colocalization between α2A-AR-IR and TH-IR could not be detected. SP, Substance P; CGRP, calcitonin gene-related peptide; ENK, <t>leuenkephalin;</t> DβH, dopamine β-hydroxylase; TH, tyrosine hydroxylase.
    Mouse Anti Leuenkephalin, supplied by BioIVT 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/mouse+anti-leuenkephalin/mouse+anti+leuenkephalin/pmc06793037-61-78-81
    Average 90 stars, based on 1 article reviews
    mouse anti-leuenkephalin - by Bioz Stars, 2026-10
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    Images

    1) Product Images from "Differential Distribution of α 2A and α 2C Adrenergic Receptor Immunoreactivity in the Rat Spinal Cord"

    Article Title: Differential Distribution of α 2A and α 2C Adrenergic Receptor Immunoreactivity in the Rat Spinal Cord

    Journal: The Journal of Neuroscience

    doi: 10.1523/JNEUROSCI.18-15-05928.1998

    Characterization of α2A-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2A-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U) depicts α2A-AR-IR (red). The second column (B, F, J,N, R, V) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column(C, G, K,O, S, W) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column(D, H, L,P, T, X) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2A-AR -IR and α2C-AR-IR are rarely colocalized. Row 2(E–H) demonstrates that α2A-AR-IR and SP-IR are highly colocalized. Row 3 (I–L) demonstrates that α2A-AR-IR and CGRP-IR fibers are highly, but not exclusively, colocalized. Row 4(M–P) demonstrates that α2A-AR-IR and ENK-IR are rarely colocalized. Row 5 (Q–T) demonstrates that α2A-AR-IR and DβH-IR are closely apposed, but not colocalized. Similarly, row 6(U–X) demonstrates that instances of colocalization between α2A-AR-IR and TH-IR could not be detected. SP, Substance P; CGRP, calcitonin gene-related peptide; ENK, leuenkephalin; DβH, dopamine β-hydroxylase; TH, tyrosine hydroxylase.
    Figure Legend Snippet: Characterization of α2A-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2A-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U) depicts α2A-AR-IR (red). The second column (B, F, J,N, R, V) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column(C, G, K,O, S, W) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column(D, H, L,P, T, X) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2A-AR -IR and α2C-AR-IR are rarely colocalized. Row 2(E–H) demonstrates that α2A-AR-IR and SP-IR are highly colocalized. Row 3 (I–L) demonstrates that α2A-AR-IR and CGRP-IR fibers are highly, but not exclusively, colocalized. Row 4(M–P) demonstrates that α2A-AR-IR and ENK-IR are rarely colocalized. Row 5 (Q–T) demonstrates that α2A-AR-IR and DβH-IR are closely apposed, but not colocalized. Similarly, row 6(U–X) demonstrates that instances of colocalization between α2A-AR-IR and TH-IR could not be detected. SP, Substance P; CGRP, calcitonin gene-related peptide; ENK, leuenkephalin; DβH, dopamine β-hydroxylase; TH, tyrosine hydroxylase.

    Techniques Used: Labeling

    Characterization of α2C-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2C-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U,Y) depicts α2C-AR-IR (red). The second column(B, F, J,N, R, V, Z) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column (C, G, K,O, S, W,AA) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column (D, H, L,P, T, X,BB) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2C-AR-IR and SP-IR are rarely colocalized. Row 2 (E–H) demonstrates that α2C-AR-IR and CGRP-IR fibers are moderately colocalized.Row 3 (I–L) demonstrates that α2C-AR-IR and somatostatin-IR fibers are moderately colocalized. Row 4 (M–P) demonstrates that α2C-AR-IR and ENK-IR are moderately colocalized. Row 5(Q–T) demonstrates that α2C-AR-IR and NK-1R are not colocalized. Row 6 (U–X) demonstrates that α2C-AR-IR and GFAP-IR are very rarely colocalized.Row 7 (Y–BB) demonstrates that α2C-AR-IR and DβH-IR are not colocalized. A similar lack of colocalization was observed between α2C-AR-IR and TH-IR (data not shown). SP, Substance P; CGRP, calcitonin gene-related peptide; SOM, somatostatin; ENK, leuenkephalin; NK-1R, NK-1 receptor; GFAP, glial fibrillary acidic protein; DβH, dopamine β-hydroxylase.
    Figure Legend Snippet: Characterization of α2C-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2C-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U,Y) depicts α2C-AR-IR (red). The second column(B, F, J,N, R, V, Z) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column (C, G, K,O, S, W,AA) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column (D, H, L,P, T, X,BB) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2C-AR-IR and SP-IR are rarely colocalized. Row 2 (E–H) demonstrates that α2C-AR-IR and CGRP-IR fibers are moderately colocalized.Row 3 (I–L) demonstrates that α2C-AR-IR and somatostatin-IR fibers are moderately colocalized. Row 4 (M–P) demonstrates that α2C-AR-IR and ENK-IR are moderately colocalized. Row 5(Q–T) demonstrates that α2C-AR-IR and NK-1R are not colocalized. Row 6 (U–X) demonstrates that α2C-AR-IR and GFAP-IR are very rarely colocalized.Row 7 (Y–BB) demonstrates that α2C-AR-IR and DβH-IR are not colocalized. A similar lack of colocalization was observed between α2C-AR-IR and TH-IR (data not shown). SP, Substance P; CGRP, calcitonin gene-related peptide; SOM, somatostatin; ENK, leuenkephalin; NK-1R, NK-1 receptor; GFAP, glial fibrillary acidic protein; DβH, dopamine β-hydroxylase.

    Techniques Used: Labeling

    Related Articles

    Labeling:

    Article Title: Differential Distribution of α2Aand α2CAdrenergic Receptor Immunoreactivity in the Rat Spinal Cord
    Article Snippet: Primary antisera were used at the following dilutions: rabbit anti-a2AAR, 1:1000; rabbit anti-a2C-AR, 1:1000; guinea pig anti-a2C-AR, 1:500; mouse anti-calcitonin gene-related peptide (CGRP), 1:2000 (Research Biochemicals, Natick, MA); mouse anti-dopamine-b-hydroxylase, 1:500 (Chemicon, Temecula, CA); rat anti-substance P (SP), 1:1000 (Research Biochemicals); rabbit anti-neurokinin-1 receptor (NK-1R) 1:500 (Vigna et al., 1994; a gift from Dr. P. Mantyh, University of Minnesota, Minneapolis, MN); rabbit anti-somatostatin, 1:1000 (Seybold and Elde, 1980); mouse anti-leuenkephalin, 1:500 (Sera-Lab, Sussex, UK); mouse antityrosine hydroxylase, 1:500 (IncStar, Stillwater, MN); guinea pig antipreprodynorphin, 1:500 (Arvidsson et al., 1995b); and mouse anti-GFAP, 1:500 (Sigma).



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    BioIVT Inc mouse anti-leuenkephalin
    Characterization of α2A-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2A-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U) depicts α2A-AR-IR (red). The second column (B, F, J,N, R, V) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column(C, G, K,O, S, W) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column(D, H, L,P, T, X) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2A-AR -IR and α2C-AR-IR are rarely colocalized. Row 2(E–H) demonstrates that α2A-AR-IR and SP-IR are highly colocalized. Row 3 (I–L) demonstrates that α2A-AR-IR and CGRP-IR fibers are highly, but not exclusively, colocalized. Row 4(M–P) demonstrates that α2A-AR-IR and ENK-IR are rarely colocalized. Row 5 (Q–T) demonstrates that α2A-AR-IR and DβH-IR are closely apposed, but not colocalized. Similarly, row 6(U–X) demonstrates that instances of colocalization between α2A-AR-IR and TH-IR could not be detected. SP, Substance P; CGRP, calcitonin gene-related peptide; ENK, <t>leuenkephalin;</t> DβH, dopamine β-hydroxylase; TH, tyrosine hydroxylase.
    Mouse Anti Leuenkephalin, supplied by BioIVT 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/mouse+anti-leuenkephalin/mouse+anti+leuenkephalin/pmc06793037-61-78-81
    Average 90 stars, based on 1 article reviews
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    Image Search Results


    Characterization of α2A-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2A-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U) depicts α2A-AR-IR (red). The second column (B, F, J,N, R, V) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column(C, G, K,O, S, W) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column(D, H, L,P, T, X) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2A-AR -IR and α2C-AR-IR are rarely colocalized. Row 2(E–H) demonstrates that α2A-AR-IR and SP-IR are highly colocalized. Row 3 (I–L) demonstrates that α2A-AR-IR and CGRP-IR fibers are highly, but not exclusively, colocalized. Row 4(M–P) demonstrates that α2A-AR-IR and ENK-IR are rarely colocalized. Row 5 (Q–T) demonstrates that α2A-AR-IR and DβH-IR are closely apposed, but not colocalized. Similarly, row 6(U–X) demonstrates that instances of colocalization between α2A-AR-IR and TH-IR could not be detected. SP, Substance P; CGRP, calcitonin gene-related peptide; ENK, leuenkephalin; DβH, dopamine β-hydroxylase; TH, tyrosine hydroxylase.

    Journal: The Journal of Neuroscience

    Article Title: Differential Distribution of α 2A and α 2C Adrenergic Receptor Immunoreactivity in the Rat Spinal Cord

    doi: 10.1523/JNEUROSCI.18-15-05928.1998

    Figure Lengend Snippet: Characterization of α2A-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2A-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U) depicts α2A-AR-IR (red). The second column (B, F, J,N, R, V) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column(C, G, K,O, S, W) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column(D, H, L,P, T, X) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2A-AR -IR and α2C-AR-IR are rarely colocalized. Row 2(E–H) demonstrates that α2A-AR-IR and SP-IR are highly colocalized. Row 3 (I–L) demonstrates that α2A-AR-IR and CGRP-IR fibers are highly, but not exclusively, colocalized. Row 4(M–P) demonstrates that α2A-AR-IR and ENK-IR are rarely colocalized. Row 5 (Q–T) demonstrates that α2A-AR-IR and DβH-IR are closely apposed, but not colocalized. Similarly, row 6(U–X) demonstrates that instances of colocalization between α2A-AR-IR and TH-IR could not be detected. SP, Substance P; CGRP, calcitonin gene-related peptide; ENK, leuenkephalin; DβH, dopamine β-hydroxylase; TH, tyrosine hydroxylase.

    Article Snippet: Primary antisera were used at the following dilutions: rabbit anti-α 2A -AR, 1:1000; rabbit anti-α 2C -AR, 1:1000; guinea pig anti-α 2C -AR, 1:500; mouse anti-calcitonin gene-related peptide (CGRP), 1:2000 (Research Biochemicals, Natick, MA); mouse anti-dopamine-β-hydroxylase, 1:500 (Chemicon, Temecula, CA); rat anti-substance P (SP), 1:1000 (Research Biochemicals); rabbit anti-neurokinin-1 receptor (NK-1R) 1:500 ( Vigna et al., 1994 ; a gift from Dr. P. Mantyh, University of Minnesota, Minneapolis, MN); rabbit anti-somatostatin, 1:1000 ( Seybold and Elde, 1980 ); mouse anti-leuenkephalin, 1:500 (Sera-Lab, Sussex, UK); mouse anti-tyrosine hydroxylase, 1:500 (IncStar, Stillwater, MN); guinea pig anti-preprodynorphin, 1:500 ( Arvidsson et al., 1995b ); and mouse anti-GFAP, 1:500 (Sigma).

    Techniques: Labeling

    Characterization of α2C-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2C-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U,Y) depicts α2C-AR-IR (red). The second column(B, F, J,N, R, V, Z) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column (C, G, K,O, S, W,AA) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column (D, H, L,P, T, X,BB) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2C-AR-IR and SP-IR are rarely colocalized. Row 2 (E–H) demonstrates that α2C-AR-IR and CGRP-IR fibers are moderately colocalized.Row 3 (I–L) demonstrates that α2C-AR-IR and somatostatin-IR fibers are moderately colocalized. Row 4 (M–P) demonstrates that α2C-AR-IR and ENK-IR are moderately colocalized. Row 5(Q–T) demonstrates that α2C-AR-IR and NK-1R are not colocalized. Row 6 (U–X) demonstrates that α2C-AR-IR and GFAP-IR are very rarely colocalized.Row 7 (Y–BB) demonstrates that α2C-AR-IR and DβH-IR are not colocalized. A similar lack of colocalization was observed between α2C-AR-IR and TH-IR (data not shown). SP, Substance P; CGRP, calcitonin gene-related peptide; SOM, somatostatin; ENK, leuenkephalin; NK-1R, NK-1 receptor; GFAP, glial fibrillary acidic protein; DβH, dopamine β-hydroxylase.

    Journal: The Journal of Neuroscience

    Article Title: Differential Distribution of α 2A and α 2C Adrenergic Receptor Immunoreactivity in the Rat Spinal Cord

    doi: 10.1523/JNEUROSCI.18-15-05928.1998

    Figure Lengend Snippet: Characterization of α2C-AR-IR fibers in rat spinal cord. Single sections of lumbar spinal cord were double-labeled with α2C-AR antisera in combination with various other antisera. The first column(A, E, I,M, Q, U,Y) depicts α2C-AR-IR (red). The second column(B, F, J,N, R, V, Z) depicts immunoreactivity obtained with other antisera used in double-labeling (green). The third column (C, G, K,O, S, W,AA) depicts digitally merged images of the first two columns. In merged images, the appearance of yellow may indicate colocalization, although higher magnification is required to distinguish colocalization from close apposition. The fourth column (D, H, L,P, T, X,BB) depicts merged images obtained at higher magnification. Row 1(A–D) demonstrates that α2C-AR-IR and SP-IR are rarely colocalized. Row 2 (E–H) demonstrates that α2C-AR-IR and CGRP-IR fibers are moderately colocalized.Row 3 (I–L) demonstrates that α2C-AR-IR and somatostatin-IR fibers are moderately colocalized. Row 4 (M–P) demonstrates that α2C-AR-IR and ENK-IR are moderately colocalized. Row 5(Q–T) demonstrates that α2C-AR-IR and NK-1R are not colocalized. Row 6 (U–X) demonstrates that α2C-AR-IR and GFAP-IR are very rarely colocalized.Row 7 (Y–BB) demonstrates that α2C-AR-IR and DβH-IR are not colocalized. A similar lack of colocalization was observed between α2C-AR-IR and TH-IR (data not shown). SP, Substance P; CGRP, calcitonin gene-related peptide; SOM, somatostatin; ENK, leuenkephalin; NK-1R, NK-1 receptor; GFAP, glial fibrillary acidic protein; DβH, dopamine β-hydroxylase.

    Article Snippet: Primary antisera were used at the following dilutions: rabbit anti-α 2A -AR, 1:1000; rabbit anti-α 2C -AR, 1:1000; guinea pig anti-α 2C -AR, 1:500; mouse anti-calcitonin gene-related peptide (CGRP), 1:2000 (Research Biochemicals, Natick, MA); mouse anti-dopamine-β-hydroxylase, 1:500 (Chemicon, Temecula, CA); rat anti-substance P (SP), 1:1000 (Research Biochemicals); rabbit anti-neurokinin-1 receptor (NK-1R) 1:500 ( Vigna et al., 1994 ; a gift from Dr. P. Mantyh, University of Minnesota, Minneapolis, MN); rabbit anti-somatostatin, 1:1000 ( Seybold and Elde, 1980 ); mouse anti-leuenkephalin, 1:500 (Sera-Lab, Sussex, UK); mouse anti-tyrosine hydroxylase, 1:500 (IncStar, Stillwater, MN); guinea pig anti-preprodynorphin, 1:500 ( Arvidsson et al., 1995b ); and mouse anti-GFAP, 1:500 (Sigma).

    Techniques: Labeling