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antifibroblast marker er tr7 rat monoclonal antibodies mabs  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology antifibroblast marker er tr7 rat monoclonal antibodies mabs
    Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ <t>mAbs</t> (smooth muscle actin <t>monoclonal</t> antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.
    Antifibroblast Marker Er Tr7 Rat Monoclonal Antibodies Mabs, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 122 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rat+antifibroblast+marker/Fibroblast+Marker+Antibody/10__1097_slash_qad__0000000000000636-68-15-24
    Average 94 stars, based on 122 article reviews
    antifibroblast marker er tr7 rat monoclonal antibodies mabs - by Bioz Stars, 2026-10
    94/100 stars

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    1) Product Images from "Role of intestinal myofibroblasts in HIV-associated intestinal collagen deposition and immune reconstitution following combination antiretroviral therapy"

    Article Title: Role of intestinal myofibroblasts in HIV-associated intestinal collagen deposition and immune reconstitution following combination antiretroviral therapy

    Journal: AIDS

    doi: 10.1097/qad.0000000000000636

    Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ mAbs (smooth muscle actin monoclonal antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.
    Figure Legend Snippet: Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ mAbs (smooth muscle actin monoclonal antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.

    Techniques Used: Bioprocessing, Activation Assay, Microscopy, Marker

    Fig. 4. Intestinal myofibroblasts are abundant in intestinal lamina propria of HIV-positive patients and express Toll-like receptor 4. Intestinal myofibroblasts (IMFs) are abundant in intestinal lamina propria of both HIV-negative and HIV-positive patients and express Toll-like receptor (TLR)4. Confocal microscopy analysis of longitudinally displayed duodenal sections. DAPI (40,6-diamidino-2-phenylindole) was used to identify nuclei of cells (blue), antifibroblast marker CD90 mAbs (green), and fibroblasts activation protein (FAP) (red) was used to identify activated mesenchymal stromal fibroblasts/myofibroblasts in duodenal mucosa. TLR4 was detected using anti-TLR4 mAbs (clone HTA125). Faint staining for FAP and collagen A in HIV-negative tissue is typical for normal controls. Merged images demonstrated co-localization between CD90 and TLR4, yellow-orange coloring.
    Figure Legend Snippet: Fig. 4. Intestinal myofibroblasts are abundant in intestinal lamina propria of HIV-positive patients and express Toll-like receptor 4. Intestinal myofibroblasts (IMFs) are abundant in intestinal lamina propria of both HIV-negative and HIV-positive patients and express Toll-like receptor (TLR)4. Confocal microscopy analysis of longitudinally displayed duodenal sections. DAPI (40,6-diamidino-2-phenylindole) was used to identify nuclei of cells (blue), antifibroblast marker CD90 mAbs (green), and fibroblasts activation protein (FAP) (red) was used to identify activated mesenchymal stromal fibroblasts/myofibroblasts in duodenal mucosa. TLR4 was detected using anti-TLR4 mAbs (clone HTA125). Faint staining for FAP and collagen A in HIV-negative tissue is typical for normal controls. Merged images demonstrated co-localization between CD90 and TLR4, yellow-orange coloring.

    Techniques Used: Confocal Microscopy, Marker, Activation Assay, Staining

    Related Articles

    Marker:

    Article Title: Protease-activated receptor 2, rather than protease-activated receptor 1, contributes to the aggressive properties of synovial fibroblasts in rheumatoid arthritis.
    Article Snippet: The PAR-1 antagonist (SCH79797) was from Axon Medchem, while the PAR-2 antagonist (ENMD10680) was from Enzo Life Sciences. .. PAR-1 and PAR-2 antibodies, rabbit anti-ERK, phospho-ERK, p38, and phospho-p38 antibodies, a rat antifibroblast marker (ERTR7), fluorescein isothiocyanate–conjugated anti-rat IgG2a, and validated PAR-1 and PAR-2 small interfering RNA (siRNA) were from Santa Cruz Biotechnology. .. Recombinant APC was from Eli Lilly, while the N-TER Nanoparticle siRNA Transfection System, recombinant TNF , and anti-human -actin antibodies were from Sigma.

    Small Interfering RNA:

    Article Title: Protease-activated receptor 2, rather than protease-activated receptor 1, contributes to the aggressive properties of synovial fibroblasts in rheumatoid arthritis.
    Article Snippet: The PAR-1 antagonist (SCH79797) was from Axon Medchem, while the PAR-2 antagonist (ENMD10680) was from Enzo Life Sciences. .. PAR-1 and PAR-2 antibodies, rabbit anti-ERK, phospho-ERK, p38, and phospho-p38 antibodies, a rat antifibroblast marker (ERTR7), fluorescein isothiocyanate–conjugated anti-rat IgG2a, and validated PAR-1 and PAR-2 small interfering RNA (siRNA) were from Santa Cruz Biotechnology. .. Recombinant APC was from Eli Lilly, while the N-TER Nanoparticle siRNA Transfection System, recombinant TNF , and anti-human -actin antibodies were from Sigma.



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    antifibroblast marker er tr7 rat monoclonal antibodies mabs  (Santa Cruz Biotechnology)
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    Santa Cruz Biotechnology antifibroblast marker er tr7 rat monoclonal antibodies mabs
    Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ <t>mAbs</t> (smooth muscle actin <t>monoclonal</t> antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.
    Antifibroblast Marker Er Tr7 Rat Monoclonal Antibodies Mabs, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rat+antifibroblast+marker/Fibroblast+Marker+Antibody/10__1097_slash_qad__0000000000000636-68-15-24
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    antifibroblast marker er tr7 rat monoclonal antibodies mabs - by Bioz Stars, 2026-10
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    rat antifibroblast marker  (Santa Cruz Biotechnology)
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    Santa Cruz Biotechnology rat antifibroblast marker
    Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ <t>mAbs</t> (smooth muscle actin <t>monoclonal</t> antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.
    Rat Antifibroblast Marker, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rat+antifibroblast+marker/Fibroblast+Marker+Antibody/pm21905006-66-12-31
    Average 94 stars, based on 1 article reviews
    rat antifibroblast marker - by Bioz Stars, 2026-10
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    Image Search Results


    Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ mAbs (smooth muscle actin monoclonal antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.

    Journal: AIDS

    Article Title: Role of intestinal myofibroblasts in HIV-associated intestinal collagen deposition and immune reconstitution following combination antiretroviral therapy

    doi: 10.1097/qad.0000000000000636

    Figure Lengend Snippet: Fig. 3. Intestinal myofibroblasts are source of collagen in HIV disease. Anti-a-SMAþ mAbs (smooth muscle actin monoclonal antibodies) (clone 1A4) were used to detect myofibroblasts (shown in green), rabbit polyclonal fluorochrome conjugated anti-FAP Abs were used to analyze activation of IMFs (shown in red), collagen A deposition was detected by second harmonic generation (SHG) analysis (shown in blue) using two-photon microscopy. Increase in a ‘filament’ type fully formed collagen A in HIV-positive duodenal mucosa is adjacent to the a-SMAþ IMFs (in green), which also express marker of activation, FAP, and result in formation of orange-yellow color on merged images. FAP, fibroblasts activation protein; IMF, intestinal myofibroblast.

    Article Snippet: The samples were then incubated with the mixture of the following antibodies: 1 mg/ml of antifibroblast marker ER-TR7 rat monoclonal antibodies (mAbs) (clone ER-TR7; Santa Cruz Biotech Inc., California, USA) conjugated to AF-546, anti-a-smooth muscle actin (SMA) monoclonal Abs (clone 1A4; Sigma), anti-CD90 (Clone 5E10; eBioscience, Inc., San Diego, California, USA) conjugated with AF-488, or TLR4 was detected using anti-TLR4 mAbs (clone HTA125; eBioscience) for 30 min at room temperature.

    Techniques: Bioprocessing, Activation Assay, Microscopy, Marker

    Fig. 4. Intestinal myofibroblasts are abundant in intestinal lamina propria of HIV-positive patients and express Toll-like receptor 4. Intestinal myofibroblasts (IMFs) are abundant in intestinal lamina propria of both HIV-negative and HIV-positive patients and express Toll-like receptor (TLR)4. Confocal microscopy analysis of longitudinally displayed duodenal sections. DAPI (40,6-diamidino-2-phenylindole) was used to identify nuclei of cells (blue), antifibroblast marker CD90 mAbs (green), and fibroblasts activation protein (FAP) (red) was used to identify activated mesenchymal stromal fibroblasts/myofibroblasts in duodenal mucosa. TLR4 was detected using anti-TLR4 mAbs (clone HTA125). Faint staining for FAP and collagen A in HIV-negative tissue is typical for normal controls. Merged images demonstrated co-localization between CD90 and TLR4, yellow-orange coloring.

    Journal: AIDS

    Article Title: Role of intestinal myofibroblasts in HIV-associated intestinal collagen deposition and immune reconstitution following combination antiretroviral therapy

    doi: 10.1097/qad.0000000000000636

    Figure Lengend Snippet: Fig. 4. Intestinal myofibroblasts are abundant in intestinal lamina propria of HIV-positive patients and express Toll-like receptor 4. Intestinal myofibroblasts (IMFs) are abundant in intestinal lamina propria of both HIV-negative and HIV-positive patients and express Toll-like receptor (TLR)4. Confocal microscopy analysis of longitudinally displayed duodenal sections. DAPI (40,6-diamidino-2-phenylindole) was used to identify nuclei of cells (blue), antifibroblast marker CD90 mAbs (green), and fibroblasts activation protein (FAP) (red) was used to identify activated mesenchymal stromal fibroblasts/myofibroblasts in duodenal mucosa. TLR4 was detected using anti-TLR4 mAbs (clone HTA125). Faint staining for FAP and collagen A in HIV-negative tissue is typical for normal controls. Merged images demonstrated co-localization between CD90 and TLR4, yellow-orange coloring.

    Article Snippet: The samples were then incubated with the mixture of the following antibodies: 1 mg/ml of antifibroblast marker ER-TR7 rat monoclonal antibodies (mAbs) (clone ER-TR7; Santa Cruz Biotech Inc., California, USA) conjugated to AF-546, anti-a-smooth muscle actin (SMA) monoclonal Abs (clone 1A4; Sigma), anti-CD90 (Clone 5E10; eBioscience, Inc., San Diego, California, USA) conjugated with AF-488, or TLR4 was detected using anti-TLR4 mAbs (clone HTA125; eBioscience) for 30 min at room temperature.

    Techniques: Confocal Microscopy, Marker, Activation Assay, Staining