massarray® typer v4.0 software Search Results


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agena bioscience typer viewer v 4 0 26 75 software
Typer Viewer V 4 0 26 75 Software, supplied by agena bioscience, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sequenom massarray typer analyzer v4 0
Massarray Typer Analyzer V4 0, supplied by Sequenom, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SYSTAT tablecurve 3d v 4 0
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GraphPad Software Inc graphpad prism v.4.0
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SYSTAT lilliefors correction
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SAS institute sas software v.9.4
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Applied Maths gelcompar, v. 4.0
Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.
Gelcompar, V. 4.0, supplied by Applied Maths, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TomoTherapy hi-art treatment-planning system v4.0
Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.
Hi Art Treatment Planning System V4.0, supplied by TomoTherapy, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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RStudio rstudio v4.0.2
Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.
Rstudio V4.0.2, supplied by RStudio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Arraystar inc v4.0
Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.
V4.0, supplied by Arraystar inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Ridom GmbH seqsphere+ v.4.0
Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.
Seqsphere+ V.4.0, supplied by Ridom GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Ridom GmbH ridom seqsphere+ v.4.0
Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.
Ridom Seqsphere+ V.4.0, supplied by Ridom GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.

Journal:

Article Title: Detection of Anionic Antimicrobial Peptides in Ovine Bronchoalveolar Lavage Fluid and Respiratory Epithelium

doi:

Figure Lengend Snippet: Western blot of ovine tracheal epithelium and lung homogenate. Lane 1, protein ladder (10 to 200 kDa) standard; lane 2, tracheal-cell homogenate stained with Coomassie blue; lane 3, tracheal-cell homogenate probed with antibody PAB96-1; lane 4, lung homogenate probed with antibody PAB96-1; lane 5, lung homogenate stained with Coomassie blue; lane 6, protein ladder standard. In tracheal epithelial cells, antibody PAB96-1 identified four bands with molecular masses of 53.7, 31.2, 28.0, and 25.7 kDa. In the lung, antibody PAB96-1 identified five bands with molecular masses of 53.5, 37.1, 31.2, 28.0, and 25.7 kDa. Identical results were seen with antibody 1G9-1C2 (data not shown). As controls, strips of membrane containing separated tracheal and lung proteins were incubated with preimmunized rabbit serum (1:200), preimmunized mouse serum (1:200), or peroxidase-labeled goat anti-rabbit IgG (0.5 μg/ml) or goat anti-mouse IgG (0.5 μg/ml). No reactions were seen (data not shown). In addition, preincubation of antibody PAB96-1 (5 μg/ml) or 1G9-1C2 (5 μg/ml) with 1.0 mM H-DDDDDDD-OH eliminated specific staining of all bands (data not shown). Blots were photographed (digital camera RD-175; Minolta), and the sizes of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths) by extrapolation from a standard curve of the sizes of the stained bands on the protein ladder.

Article Snippet: Blots were photographed (digital camera RD-175; Minolta, Ramsey, N.J.), and the molecular masses of the reactive bands were determined (GelCompar, v. 4.0; Applied Maths, Kortrijk, Belgium) by extrapolation from a standard curve of the molecular masses of the prestained bands on the protein ladder.

Techniques: Western Blot, Staining, Incubation, Labeling