e coli neb 5 alpha Search Results


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Representation of immunoblot analysis of the cell lysate of <t>E.</t> <t>coli</t> expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.
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Representation of immunoblot analysis of the cell lysate of <t>E.</t> <t>coli</t> expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.
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GeneSearch Inc neb® 5-alpha e. coli cells
Representation of immunoblot analysis of the cell lysate of <t>E.</t> <t>coli</t> expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.
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Infors AG e. coli neb 5-alpha
Representation of immunoblot analysis of the cell lysate of <t>E.</t> <t>coli</t> expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.
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Glentham Life Sciences virus strains neb 5 alpha competent e coli neb c2988j one shot bl21 star
Representation of immunoblot analysis of the cell lysate of <t>E.</t> <t>coli</t> expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.
Virus Strains Neb 5 Alpha Competent E Coli Neb C2988j One Shot Bl21 Star, supplied by Glentham Life Sciences, 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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Image Search Results


Journal: iScience

Article Title: Multifaceted role of RNA editing in promoting loss-of-function of PODXL in cancer

doi: 10.1016/j.isci.2022.104836

Figure Lengend Snippet:

Article Snippet: NEB 5-alpha Competent E.coli (High Efficiency) , NEB , Cat# C2987H.

Techniques: Recombinant, Transfection, SYBR Green Assay, Protease Inhibitor, Staining, Bradford Assay, Fractionation, Cell Culture, Plasmid Preparation, Clone Assay, Software

Representation of immunoblot analysis of the cell lysate of E. coli expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.

Journal: bioRxiv

Article Title: Molecular basis for recognition of the Group A Carbohydrate backbone by the PlyC streptococcal bacteriophage endolysin

doi: 10.1101/2021.03.19.436156

Figure Lengend Snippet: Representation of immunoblot analysis of the cell lysate of E. coli expressing the SCC and GAC pRha and carrying an empty control plasmid (−ve). A) Blot was incubated with PlyCB-Alexa Fluor ® 647 (PlyCB WT AF647 ). B) Probing the same samples with the GAC antibodies confirms the presence of GAC in the bands. Molecular mass markers are given in kDa.

Article Snippet: E. coli genotypes DH5 α (NEB, cat. No. C2988J), DH10 α (Thermo Fisher, cat No. 18297010), BL21 (NEB, cat No. C2530H) and Origami 2 (Millipore Sigma, cat. No. 71346) were used for routine plasmid propagation or protein expression and grown in Lysogeny Broth (LB) medium supplemented with either 50 µg/ml kanamycin, 100 µg/ml ampicillin or 35 µg/ml chloramphenicol as needed.

Techniques: Western Blot, Expressing, Plasmid Preparation, Incubation

PlyCB binding to E. coli cells were investigated by flow cytometry after labelling with PlyCB WT AF647 and PlyCB R66E AF647 mutant proteins. Blue: −ve control cells without pRha. Red: pRha producing E. coli cells. Representative histograms are shown. A) Left panel: unstained cells. Right panel: The anti-GAC antibodies (GAC-FITC) were used as a positive control to label the E. coli cells producing pRha. The antibodies do not bind to the E. coli cells carrying an empty plasmid (−ve).B) Left panel: PlyCB WT AF647 binds to the E. coli cells producing pRha, but not to the E. coli cells carrying an empty plasmid (−ve). Right panel: PlyCB R66E AF647 does not binds to the E. coli cells producing pRha.

Journal: bioRxiv

Article Title: Molecular basis for recognition of the Group A Carbohydrate backbone by the PlyC streptococcal bacteriophage endolysin

doi: 10.1101/2021.03.19.436156

Figure Lengend Snippet: PlyCB binding to E. coli cells were investigated by flow cytometry after labelling with PlyCB WT AF647 and PlyCB R66E AF647 mutant proteins. Blue: −ve control cells without pRha. Red: pRha producing E. coli cells. Representative histograms are shown. A) Left panel: unstained cells. Right panel: The anti-GAC antibodies (GAC-FITC) were used as a positive control to label the E. coli cells producing pRha. The antibodies do not bind to the E. coli cells carrying an empty plasmid (−ve).B) Left panel: PlyCB WT AF647 binds to the E. coli cells producing pRha, but not to the E. coli cells carrying an empty plasmid (−ve). Right panel: PlyCB R66E AF647 does not binds to the E. coli cells producing pRha.

Article Snippet: E. coli genotypes DH5 α (NEB, cat. No. C2988J), DH10 α (Thermo Fisher, cat No. 18297010), BL21 (NEB, cat No. C2530H) and Origami 2 (Millipore Sigma, cat. No. 71346) were used for routine plasmid propagation or protein expression and grown in Lysogeny Broth (LB) medium supplemented with either 50 µg/ml kanamycin, 100 µg/ml ampicillin or 35 µg/ml chloramphenicol as needed.

Techniques: Binding Assay, Flow Cytometry, Mutagenesis, Positive Control, Plasmid Preparation