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Uvp chemstudio imager

Manufactured by Analytik Jena
Sourced in Germany

The UVP ChemStudio imager is a compact and versatile imaging system designed for a wide range of applications in molecular biology and biochemistry laboratories. It is capable of capturing high-quality images of gels, blots, and other samples illuminated with UV, visible, or chemiluminescent light sources.

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5 protocols using uvp chemstudio imager

1

SDS-PAGE Protein Separation and Sypro Staining

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SDS-PAGE was run on a PhastGel gradient (10–15%) minigel system (GE Healthcare, Munich, Germany). For Sypro staining, proteins were fixed on the gel for 2 × 30 min in 50% MeOH and 7% acetic acid. The gel was then incubated with 2 ml Sypro Ruby protein stain (Sigma-Aldrich; Merck, Darmstadt, Germany) overnight at room temperature. After 30 min washing in 10% MeOH and 7% acetic acid and additional washing for 10 min in H2O, fluorescence signals were detected on a UVP ChemStudio imager (Analytik Jena, Jena, Germany).
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2

SDS-PAGE and Western Blotting Protocol

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SDS-PAGE was performed on NovexTM WedgeWellTM 8–16% Tris-Glycine gels (Invitrogen; Thermo Fisher Scientific, Waltham, USA) for 90 min at 125 V. After electrophoresis, proteins were blotted to a PVDF-P membrane (Millipore; Merck, Darmstadt, Germany), which was blocked in 3% casein-PBS and incubated for 1 h at room temperature with 2 μg/ml mAb 1A11 or with the rabbit antiserum (1:1000). The membrane was washed three times in PBS with 0.1% Tween 20 and incubated overnight with rabbit anti-mouse- or goat anti-rabbit-HRP (horseradish peroxidase) conjugate (Dako; Merck, Darmstadt, Germany) diluted 1:2000 in 1% casein-PBS. After three further washing steps in PBS with 0.1% Tween 20 and two in PBS, Super Signal Western Femto (Pierce; Thermo Fisher Scientific, Waltham, MA, USA) was applied and chemiluminescence signals were detected on a UVP ChemStudio imager (Analytik Jena, Jena, Germany).
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3

Western Blot Detection of Hbl B

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For Western blotting, 30 µl protein solution or B. cereus culture supernatant were applied to Criterion XT precast gels (BioRad Laboratories, Feldkirchen, Germany). After electrophoresis, proteins were blotted to a PVDF-P membrane (Millipore; Merck, Darmstadt, Germany). The membrane was saturated with 3% casein-PBS and incubated for 1 h at room temperature with 2 µg/ml Strep-MAB-Classic (IBA Lifesciences, Göttingen, Germany) or monoclonal antibody (mAb) 11A5 [21 (link)] for detection of Hbl B.’ Afterward, it was washed three times in PBS with 0.1% Tween 20 and incubated overnight with a 1:2000 dilution of rabbit anti-mouse-horseradish peroxidase conjugate (Dako; Merck, Darmstadt, Germany) before three further washing steps in PBS with 0.1% Tween 20 and two in PBS. Subsequently, Super Signal Western Femto (Pierce; Thermo Fisher Scientific, Waltham, MA, USA) was applied, and chemiluminescence signals were sensed on a UVP ChemStudio imager (Analytik Jena, Jena, Germany).
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4

Western Blot Analysis of GFP Fusion Proteins

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For detection of the green fluorescent protein (GFP) fusion protein in RXR3 complementation plants, total protein was extracted as described previously (Ying et al., 2022 (link)). Equal amounts (30 µg) of each sample were separated by sodium dodecyl sulphate‐polyacrylamide gel electrophoresis (SDS‐PAGE), transferred into Immobilon‐P PVDF membrane (0.45 μm; Millipore Sigma) and probed with 1/5000‐diluted monoclonal mouse anti‐GFP horseradish peroxidase (HRP)‐conjugated antibody (Miltenyi Biotec). Chemiluminescence detection was performed with ECL™ Prime Western Blotting System (Millipore Sigma) and UVP ChemStudio imager (Analytik Jena).
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5

Immunoblotting Analysis of Pn14p Protein

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Samples of Pn14p were blotted on a PVDF membrane. The membrane was incubated in 3% BSA in PBST buffer (0.1% Tween 20 in 1× PBS, pH 7.4) for 1 h followed by a brief wash in PBST. The membrane was then incubated with polyclonal Anti-Pn14p sera (1:5000 dilution in 1% BSA PBST buffer) for 2 h at room temperature followed by four 10-min PBST washes. The membrane was then incubated with horseradish peroxidase linked anti-mouse IgG secondary antibody (1:10,000 in 1% BSA PBST) for 1 h at room temperature followed by five 10-min PBST washes. The membrane was developed using chemiluminescent substrate (Bio-Rad) and imaged on an Analytik Jena UVP ChemStudio imager. Signal densitometry was performed using the NIH ImageJ software.
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