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SeraCare Life Sciences peroxidase-based detection method
Peroxidase Based Detection Method, supplied by SeraCare Life Sciences, 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/peroxidase+based+method/peroxidase+based+detection+method/pm12557214-156-7-10
Average 90 stars, based on 1 article reviews
peroxidase-based detection method - by Bioz Stars, 2026-11
90/100 stars

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Article Title: Role for keratins 6 and 17 during wound closure in embryonic mouse skin.
Article Snippet: Injury to adult skin triggers a response designed to restore its vital barrier function.. A conserved aspect of this response is a rapid switch in gene expression whereby the type II keratin 6 (K6) and type I keratins 16 and 17 (K16, K17) are induced in epithelial cells at the wound edge.. This induction occurs at the expense of the keratins normally expressed during terminal differentiation and correlates with the activation of epithelial cells at the wound edge, ahead of their migration into the wound site.



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Expression of membrane RANKL on BC cell lines under the two different culture conditions. ( A ) <t>Immunocytochemistry</t> staining for mRANKL in the MDA-MB-231 cell line under both culture conditions (x 400 magnification). ( B ) Immunocytochemistry staining for mRANKL in the MCF-7 cell line under both culture conditions (x 400). Positive controls were performed in both BC cell lines incubated with anti-RANKL (cytoplasmatic RANKL = cRANKL, evaluated previously) and anti-AE1AE3 (a pan-cytokeratin epithelial marker). No staining was observed in both BC cell lines incubated with an irrelevant rabbit Ig Ab as a negative isotype control. Nuclei were counterstained with hematoxylin (purple).
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Expression of membrane RANKL on BC cell lines under the two different culture conditions. ( A ) Immunocytochemistry staining for mRANKL in the MDA-MB-231 cell line under both culture conditions (x 400 magnification). ( B ) Immunocytochemistry staining for mRANKL in the MCF-7 cell line under both culture conditions (x 400). Positive controls were performed in both BC cell lines incubated with anti-RANKL (cytoplasmatic RANKL = cRANKL, evaluated previously) and anti-AE1AE3 (a pan-cytokeratin epithelial marker). No staining was observed in both BC cell lines incubated with an irrelevant rabbit Ig Ab as a negative isotype control. Nuclei were counterstained with hematoxylin (purple).

Journal: Cancer Cell International

Article Title: Expression of osteoprotegerin, receptor activator of nuclear factor kappa-B ligand, tumor necrosis factor-related apoptosis-inducing ligand, stromal cell-derived factor-1 and their receptors in epithelial metastatic breast cancer cell lines

doi: 10.1186/1475-2867-12-29

Figure Lengend Snippet: Expression of membrane RANKL on BC cell lines under the two different culture conditions. ( A ) Immunocytochemistry staining for mRANKL in the MDA-MB-231 cell line under both culture conditions (x 400 magnification). ( B ) Immunocytochemistry staining for mRANKL in the MCF-7 cell line under both culture conditions (x 400). Positive controls were performed in both BC cell lines incubated with anti-RANKL (cytoplasmatic RANKL = cRANKL, evaluated previously) and anti-AE1AE3 (a pan-cytokeratin epithelial marker). No staining was observed in both BC cell lines incubated with an irrelevant rabbit Ig Ab as a negative isotype control. Nuclei were counterstained with hematoxylin (purple).

Article Snippet: According to the manufacturer’s recommendations, a peroxidase-based immunocytochemistry staining method (K0690, Dako) was used for primary Ab detection, and a 3,3′-diaminobenzidine tetrahydrochloride (DAB) substrate system (K3468, Dako) was used as the chromogen.

Techniques: Expressing, Immunocytochemistry, Staining, Incubation, Marker

Expression of membrane and cytoplasmic RANK (mRANK/cRANK), SDF-1 and CXCR4 in both BC cell lines. ( A ) Immunocytochemistry staining for RANK, SDF-1 and CXCR4 in MDA-MB-231 and MCF-7 cells grown under arrest and post-stimulation culture conditions (x 400 magnification). ( B ) The MDA-MB-231 and MCF-7 cell lines were incubated with irrelevant IgG1 and mouse Igs Abs as negative isotype controls (x 400 magnification). Nuclei were counterstained with hematoxylin (purple).

Journal: Cancer Cell International

Article Title: Expression of osteoprotegerin, receptor activator of nuclear factor kappa-B ligand, tumor necrosis factor-related apoptosis-inducing ligand, stromal cell-derived factor-1 and their receptors in epithelial metastatic breast cancer cell lines

doi: 10.1186/1475-2867-12-29

Figure Lengend Snippet: Expression of membrane and cytoplasmic RANK (mRANK/cRANK), SDF-1 and CXCR4 in both BC cell lines. ( A ) Immunocytochemistry staining for RANK, SDF-1 and CXCR4 in MDA-MB-231 and MCF-7 cells grown under arrest and post-stimulation culture conditions (x 400 magnification). ( B ) The MDA-MB-231 and MCF-7 cell lines were incubated with irrelevant IgG1 and mouse Igs Abs as negative isotype controls (x 400 magnification). Nuclei were counterstained with hematoxylin (purple).

Article Snippet: According to the manufacturer’s recommendations, a peroxidase-based immunocytochemistry staining method (K0690, Dako) was used for primary Ab detection, and a 3,3′-diaminobenzidine tetrahydrochloride (DAB) substrate system (K3468, Dako) was used as the chromogen.

Techniques: Expressing, Immunocytochemistry, Staining, Incubation

Expression of TRAIL, TRAIL-R1, TRAIL-R2, TRAIL-R3 and TRAIL-R4 in both BC cell lines. ( A ) Immunocytochemistry staining for TRAIL, TRAIL-R1, TRAIL-R2, TRAIL-R3 and TRAIL-R4 in the MDA-MB-231 and MCF-7 cell lines grown under arrest and post-stimulation culture conditions (x 400 magnification). ( B ) The MDA-MB-231 and MCF-7 cell lines were incubated with anti-AE1AE3 (positive control) and with irrelevant mouse Igs, goat IgG and IgG1 Abs as negative isotype controls (x 400 magnification). Nuclei were counterstained with hematoxylin (purple).

Journal: Cancer Cell International

Article Title: Expression of osteoprotegerin, receptor activator of nuclear factor kappa-B ligand, tumor necrosis factor-related apoptosis-inducing ligand, stromal cell-derived factor-1 and their receptors in epithelial metastatic breast cancer cell lines

doi: 10.1186/1475-2867-12-29

Figure Lengend Snippet: Expression of TRAIL, TRAIL-R1, TRAIL-R2, TRAIL-R3 and TRAIL-R4 in both BC cell lines. ( A ) Immunocytochemistry staining for TRAIL, TRAIL-R1, TRAIL-R2, TRAIL-R3 and TRAIL-R4 in the MDA-MB-231 and MCF-7 cell lines grown under arrest and post-stimulation culture conditions (x 400 magnification). ( B ) The MDA-MB-231 and MCF-7 cell lines were incubated with anti-AE1AE3 (positive control) and with irrelevant mouse Igs, goat IgG and IgG1 Abs as negative isotype controls (x 400 magnification). Nuclei were counterstained with hematoxylin (purple).

Article Snippet: According to the manufacturer’s recommendations, a peroxidase-based immunocytochemistry staining method (K0690, Dako) was used for primary Ab detection, and a 3,3′-diaminobenzidine tetrahydrochloride (DAB) substrate system (K3468, Dako) was used as the chromogen.

Techniques: Expressing, Immunocytochemistry, Staining, Incubation, Positive Control